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Volume 2013 (2013), Article ID 813648, 17 pages
Current Understanding of Guanylin Peptides Actions
Department of Physiology, School of Medicine, University of Zagreb, Salata 3, 10000 Zagreb, Croatia
Received 4 February 2013; Accepted 26 February 2013
Academic Editors: L. Espinosa, A. H. Tzamaloukas, and G.-P. Zhou
Copyright © 2013 Aleksandra Sindic. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Guanylin peptides (GPs) family includes guanylin (GN), uroguanylin (UGN), lymphoguanylin, and recently discovered renoguanylin. This growing family is proposed to be intestinal natriuretic peptides. After ingestion of a salty meal, GN and UGN are secreted into the intestinal lumen, where they inhibit sodium absorption and induce anion and water secretion. At the same conditions, those hormones stimulate renal electrolyte excretion by inducing natriuresis, kaliuresis, and diuresis and therefore prevent hypernatremia and hypervolemia after salty meals. In the intestine, a well-known receptor for GPs is guanylate cyclase C (GC-C) whose activation increases intracellular concentration of cGMP. However, in the kidney of GC-C-deficient mice, effects of GPs are unaltered, which could be by new cGMP-independent signaling pathway (G-protein-coupled receptor). This is not unusual as atrial natriuretic peptide also activates two different types of receptors: guanylate cylcase A and clearance receptor which is also G-protein coupled receptor. Physiological role of GPs in other organs (liver, pancreas, lung, sweat glands, and male reproductive system) needs to be discovered. However, it is known that they are involved in pathological conditions like cystic fibrosis, asthma, intestinal tumors, kidney and heart failure, obesity, and metabolic syndrome.
The physiological importance of digestive system is not only to digest and absorb nutrients but also to prepare the body for an increase in blood concentrations of glucose, amino acids, electrolytes, and water. It is well known that several hormones secreted by intestine after a meal, like gastrin, secretin, cholecystokinin, and especially gastric inhibitory peptide increase insulin production even before the concentrations of glucose and amino acids significantly increase in the blood. Lennane et al. in 1975 showed that salt taken per os will increase secretion of electrolyte and water by the kidneys more than the same amount of the salt given intravenously, proposing the existence of intestinal hormones that regulate kidney function . After a salty meal, intestinal natriuretic peptides also known as guanylin peptides (GPs) are secreted by intestine where the inhibit sodium absorption from intestinal lumen by inhibiting sodium/hydrogen exchange (NHE), increase bicarbonate and chloride secretion, inhibit water absorption [2, 3], and increase renal sodium and potassium secretion [4–6]. Effects of GPs on sodium transport in the intestine and the kidneys prevent postprandial hypernatremia, gastric inhibitory peptide has a major role in decreasing postprandial increase in plasmatic glucose concentration as well. The growing family of GPs has, up to date, four members: guanylin (GN), uroguanylin (UGN), lymphoguanylin, and renoguanylin. GN was the first GP isolated first from rat intestine . A year later, the most abundant GP present in the urine, UGN was isolated from opossum urine . The other two members of the GPs family: lymphoguanylin isolated from opossum lymphatic tissues  and renoguanylin found in eels . Mammalian isoform of renoguanylin is not discovered yet. However, the last two members of guanylin peptide family are up to date less investigated and their physiological functions yet need to be discovered.
The importance of GPs in maintaining the homeostasis of water and electrolyte homeostasis working together with other natriuretic peptides (like atrial natriuretic peptide) and opposite to rennin-angiotensin-aldosterone system and arginine vasopressin seems to be very relevant since GPs appeared early in evolution as they are found in all examined animals (mammals, birds, and fishes).
2. Structure and Metabolism of Guanylin Peptides
Genes for natriuretic peptides secreted by the heart (atrial natriuretic peptide (ANP) and brain natriuretic peptide (BNP)) and by intestine (GN and UGN) are located at the first human chromosome and the fourth mouse chromosome . Since GPs are by structure peptide hormones, they are synthesized as preprohormone, prohormone, and hormone (Figure 1). GN and UGN have 3 exons and 2 introns [12, 13]. Human pre-pro-GN has 115 amino acids. Is it cleaved to pro-GN which has 94 amino acids. The active hormone GN has 15 amino acids . The production of human UGN is the same. Human pre pro-UGN has 112 amino acids and it is cleaved to pro-UGN with 86 amino acids. Active human UGN has 16 amino acids [15, 16]. However, it is suggested that the circulating form of UGN has 24 amino acids . The difference in the function of those two types of UGN needs to be established.
GN and UGN have two disulfide bonds between cysteins which are essential for their activity (Figure 1) [14, 16, 22]. Today, we know that main receptor for GPs was first described as receptor for the heat-stable enterotoxin of Escherichia coli (STa) . STa has 19 amino acids and three disulfide bonds which could be the reason for its stronger and unregulated activation on the GPs receptor. Stronger activation of GPs receptor by STa leads to more potent secretion of electrolyte and water into the intestinal lumen which caused secretory diarrhea [24, 25]. Since the discovery of receptors/binding sites for STa which is exogenous enterotoxin, in intestine as well as other extraintestinal tissue like kidneys, we started to look for endogenous ligands and first discovered GN and soon after UGN.
Human GN is known as guanylate cyclase activating peptide-1; GCAP-1 consists of 15 amino acids and possesses two disulfide bonds between two cysteins (between 4–12 and 7–15 positions) (Figure 1) [14, 22]. From 15 amino acids, human GN shares similarity in 10 amino acids with GN from eel, opossum, rat, pig, and guinea pig with the highest similarity to pig GN with a difference only in 2 amino acids (Table 1). GN is present in the plasma mostly as its pro GN form in concentration of 30–40 pM [26, 27].
Human UGN is also known as guanylate cyclase activating peptide-2, GCAP-2. UGN has 16 amino acids and has two disulfide bonds between 4–12 and 7–15 positions similar to GN (Figure 1) . Eel and pig isoforms of UGN also have 16 amino acids while opossum, rat, and guinea pig UGNs have 15 amino acids while they are missing the last amino acid. UGNs from all listed species (Table 1) share 9 amino acids at particular positions . In both GN and UGN structures cysteins are preserved which are necessary for the development of disulfide bonds and activity of GPs.
In contrast to GN, 60–90% of circulating UGN in the plasma is in the form of active hormone in a concentration of 5–7 pM [29, 30]. However, those findings are still in dispute. Recently, circulating plasma pro-UGN was suggested to mediate enterorenal signaling. It is suggested that filtrated pro-UGN is cut by proteases present in the tubular lumen to the active form of UGN [31, 32]. Structural differences between GN and UGN in different species are given in Table 1.
The structural difference between GN and UGN which lies in their sensitivity towards proteases is especially important for the physiological role of the GPs in the kidney. GN has a tyrosine as its ninth amino acid which makes it sensitive to proteases, mostly chymotrypsin. UGN has an asparagine as its ninth amino acid and is therefore protected form proteases present in tubular lumen. However, in the kidney filtrated pro-UGN is not protected and could be cut by tubular proteases [33, 34]. Therefore, GN is degraded by chymotrypsin present in different parts of the kidney nephrons [4, 35] and is consequently not present in urine.
After a salty meal, the intestine is producing GPs in the gut lumen (inhibition of the water and electrolyte absorption). At the same time, intestine produces GPs into the blood. It is proposed that GPs secreted form intestine induced natriuresis, kaliuresis, and diuresis in the kidney after glomerular filtration. Intestinal GPs when located in the tubular lumen act on receptors located at apical membrane of tubular cells. Even the proteins with ten times higher molecular weight, like myoglobin, are filtrated through glomerular membrane almost as easy as water (filterability is 75% of water), suggesting that even pro-GPs present in the plasma could be sufficiently filtrated and present in the lumen of different nephron segments. However, recent research suggests that in addition to endocrine function of the GPs secreted from the intestine, the other source of GPs and their precursors in tubular lumen could be released from the kidney cells. Kidney secretes GPs only locally into the tubular lumen where they act as paracrine peptides but not in the blood .
mRNA for GPs could be found in other organs as well, like adrenal glands, reproductive system, lung, and pancreas, where the importance of GPs secretion is, as far as we known, local regulation of membrane transport systems, and it is still not very well understood [36–38]. Although the mRNA for GPs is present in numerous tissues, the intestine is considered to be the only source for GPs present in the blood [29, 39, 40].
Both endocrine and paracrine secretion of the GPs via intestine are stimulated by parasympathetic system via activation of n.vagus [41, 42]. This vagal stimulation could have importance in UGN function in the stomach while UGN is produced by enterochromaffin-like cells where acetylcholine also regulates production of histamine which regulates HCl production of the stomach . Interestingly, it is known that in patients with Zn2+ deficiency have secretory diarrhea. Cousins laboratory showed when Zn2+ deficiency is induced in rats, unregulated expression of UGN in enterocytes increased, which could explain secretory diarrhea in humans [44–47].
3. Signaling Pathways of Guanylin Peptides in the Intestine
Expression of GN and UGN in intestine is well regulated by salt ingestion. High-salt diet leads to the secretion of GN and UGN into the intestinal lumen. On the other hand, low salt intake decreases mRNA levels of GN and UGN in the rat digestive tract [3, 48], which is suggested to be a protective mechanism in how to spare sodium during periods of salt restriction in the food.
GN is mainly present in goblet and epithelial cells of the colonic mucosa while UGN presents in enterochromaffin cells of the small intestine [2, 3, 49, 50]. mRNA for GN is located from duodenum to distal colon from lower to higher expression along the intestine (Figure 2) [51, 52]. UGN is present along the gastrointestinal tract with the highest expression in the duodenum [18, 38, 49, 51, 53, 54, 77].
Proximal part of the digestive system, mainly duodenum, developed powerful mechanisms to protect epithelial cells against acid secretion from stomach. A well-know mechanism is inhibition of gastric emptying with intestinal hormones. Cholecystokinin is released from the jejunum mucosa as response to the presence of the fatty acids in intestinal lumen. Secretin is secreted in duodenum as a response to low pH duodenal content, and in addition to inhibition of stomach emptying it also induces pancreatic secretion rich in bicarbonate. UGN could play a significant role in epithelial protection by increasing pH of duodenal lumen via inhibition of hydrogen secretion (by NHE inhibition) and increase in bicarbonate secretion. The very important mechanism in those protective effects is pH sensitivity of GPs action. The effects of GN and UGN on concentration of intracellular cGMP after activation of their receptor guanylate cyclase C (GC-C) is pH dependent (Figure 3). The increase in intracellular concentration of cGMP after UGN stimulation is higher at pH 5 compared to pH 8. In opposition to that increase in cGMP, concentration induced by GN is higher at pH 8. Those findings correspond to the expression of the UGN in proximal part of digestive tract where pH is lower than in distal part where is more alkaline and GN is produced more, which potentiate effects of GPs via GC-C-, cGMP-dependent signaling pathway. Furthermore, pH sensitivity of UGN intracellular cGMP accumulation is also important in the duodenum. To neutralize the low pH after stomach empting in addition to pancreatic secretion, duodenum secretes bicarbonate. This secretion is cGMP dependent and could be a result of UGN action which is even more potentiated at low pH conditions. It was suggested by Hamra et al. (1997) that this pH dependence affects the ligand/receptor interaction depending on the N terminal ends of the UGN and GN molecules (Figure 1) .
As you can see at Figure 4. UGN increases bicarbonate secretions via CFTR, cGMP-dependent mechanism involving members of Slc26 transporter family. The Slc26 family has up to date 11 members. It exchanges Cl− with sulfate, iodide, formate, oxalate, hydroxyl ion, and bicarbonate, whereas other function as Cl− channels. Slc26a3 (DRA), Slc26a6 (PAT-1, CFEX), and Slc26a9 are involved in bicarbonate secretion in digestive tract and pancreas via CFTR-dependent pathway. Recently, Slc26a4 (pendrin) was suggested as target for UGN-dependent electrolyte transport in intercalated cells of kidney cortical collecting duct (see later) . In the future, additional research should be done to investigate the possible effects of GPs on other members of Slc26 family in the way to determine existence of CFTR-independent signaling pathway for GPs. Furthermore, UGN inhibits H+ secretion via inhibition of sodium/proton exchanger (NHE) and therefore decreases H+ concentration in the duodenum . As described above, this cGMP/GC-C-dependent UGN effects are more pronounced at acidic pH after gastric emptying, inducing stronger bicarbonate secretion, and inhibition of hydrogen secretion, which helps to lower the concentration of hydrogen ions delivered from the stomach.
In stomach, UGN is produced by enterochromaffin-like cells. Those cells are major source of histamine after stimulation with gastrin and acetylcholine. Histamine regulates HCl production of the stomach . The physiological and pathophysiological roles of UGN are the stomach are still not known; we can assume that UGN is involved in the protection of stomach from HCl by secreting bicarbonate in stomach lumen. Furthermore, GN is produced by parietal cells. After intravenous application of GN, those cells increase the production of protective mucus, which is one more protective mechanism in the stomach [56, 57].
In more details, when secreted in the gut lumen, GPs stimulate enterocytes via the membrane-bound guanylate cyclase C (GC-C) located at the apical membrane of the enterocytes. Activation of GC-C produces cGMP from GTP [7, 8]. The increase in cGMP as second messenger activates the protein kinase G II (PKG II) [58, 59] and inhibits the phosphodiesterase III (PDE III). Phosphodiesterases are divided into types concerning regulatory mechanism and substrate. PDE type III is responsible for the degradation of cAMP; therefore, inhibition of PDE III by cGMP leads to increase of intracellular concentration of cAMP which follows activation of cAMP-specific protein kinase A (PKA) [59–61]. Furthermore, cGMP partially inhibits Na+ absorption from intestinal lumen into the blood by inhibiting apical Na+/H+ exchanger type 2 (NHE2) and therefore preventing fast increase in blood sodium concentrations after the consumption of the salty meal [62, 63]. PKG II and PKA increase the secretion of Cl− via the cystic fibrosis transmembrane conductance regulator (CFTR) followed by an activation of the member of Slc26 family which exchanges bicarbonate for chloride resulting in bicarbonate secretion. Two different opinions on how bicarbonate secretion occurs in intestine lumen as well as in other organs exist. Some researchers believe that bicarbonate is transported by CFTR itself. Since GPs still stimulate bicarbonate secretion in CFTR-deficient mice, it is reasonable to believe that the CFTR has a regulatory role while bicarbonate secretion is due to activation of members of Slc26 family . Changes which follow GC-C activation in the intestine increase the amount of electrolyte in the intestinal lumen, which slows down the absorption of the water from intestinal lumen to the blood which could not be quickly excreted from the organism by the kidneys and protect from drastic increase in blood volume (Figure 4) [60, 65–67].
4. GC-C-Dependent Signaling Pathway
STa-specific binding sites are found in intestine and colon of mammals including human. Interestingly, binding sites are also found in extraintestinal tissue like gallbladder, trachea, testis, kidney, and opossum kidney cell line (OK cells) [68–70]. Since 1978, it is known that STa increased intracellular concentration of cGMP in intestine ; however, until 1990 and Schulz discovery the receptor responsible for STa effects in the gut was not known . The discovered receptor was named guanylate cyclase C because it increases intracellular cGMP concentration and it is discovered after guanylate cyclase A (GC-A) and guanylate cyclase B (GC-B) receptors for atrial natriuretic peptides. Furthermore, CaCo-2 and T84 cell lines are intestinal human carcinoma cell lines. Intracellular concentration of cGMP increases in both cell lines after GPs stimulations via guanylate cycles C, and it is a well-established model for investigation of this main signaling pathway for GPs.
Main GPs receptor, GC-C, belongs to the family of guanylate cyclases. There are 2 major types of guanylate cyclases: soluble or cytoplasmatic guanylate cyclase which is receptor for NO and CO and membrane-bound guanylate cyclases which are receptors for natruretic peptides (Table 2). Soluble guanylate cyclases are widely spread (muscles, platelets, lung, liver, kidney, heart, and CNS) and recently well investigated as receptors of NO. Up to date, 6 membrane-bound guanylate cyclases are known. GC-A (also known as natriuretic peptide receptor type A, NPR-A) is receptor for atrial natriuretic peptide (ANP); it is a kidney isoform urodilatin and brain natriuretic peptide (BNP) and is involved in electrolyte and water homeostasis by heart. GC-A is also present in numerous tissue as well as soluble guanylate cyclase (smooth muscle, kidney, adrenal gland, heart, and CNS). GC-B or natriuretic peptide receptor type B, NPR-B, has a high affinity towards CNP. It is located at fibroblasts, heart, and CNS and plays more important role in the physiology of bones and cartilage. A splice variant of this receptor, NPR-Bi, is a truncated form expressed in human tissues, also binds CNP but lacks GC-function (it does not produce cGMP as second messenger but acts as a tyrosine kinase) [71, 72]. A fourth type of receptor, the natriuretic peptide receptors type C (NPR-C) is clearance receptor and binds all four natriuretic peptides. This receptor is G-protein-coupled receptor which is missing guanylate cyclase domain and guanylate cyclase activity.
Guanylate cyclases D, E, and F (GC-D, GC-E, and GC-F) are located in sensory organs. Recently, GC-D was proposed to be a GPs receptor in olfactory system . Guanylate cyclase G (GC-G or GC-1) is an orphan receptor present in the skeletal muscle, lung, intestine, testis, and kidney [74–76]. This orphan receptor could play important role in GPs signaling mechanism instead of GC-C in the kidney (see later).
GC-C is widely spread, localized in tissues expressing other parts of GP signaling pathway like CFTR (adrenal glands, brain, the embryonic or regenerating but not adult liver, placenta, testis, airways, spleen, thymus, and lymphatic nodes) [77–79]. GC-C expression is increased in infants and prematures which could explain higher sensitivity to presence of STa in intestine and more pronounced diarrhea in children . Like other GCs, GC-C has extracellular, juxtamembrane domain, kinase homology, and catalytic domain (Figure 5).
As any other transmembrane receptor, extracellular domain is responsible for ligand binding. Juxtamembrane domain is bound to extracellular domain by transmembrane domain and it is located near the cell membrane. This domain has similar structure to parts of IGF (insulin-like growth factor) and EGF (epidermal growth factor) receptors which are responsible for binding the G-proteins [81, 82]. Kinase homology domain is similar to catalytic domain of PDGF (platelet-derived growth factor) receptors. Catalytic domain converts GTP to cGMP after ligand binding to extracellular domain. For pronounced guanylate cyclase activity of GC-C kinase, homology domain should be phosphorylated. C-terminal tail of the GC-C is unique and it is involved in binding the GC-C to cytoskeleton and important for endocytosis of ligand-receptor complexes .
Protein kinase C (PKC) is a well-established regulator of GC-C activity. PKC phosphorylates C-terminal tail of GC-C which leads to 70% increase in intracellular concentration of cGMP after STa stimulation compared to control [84–88]. For the full activity of GC-C, Mg2+-ATP should be present .
5. GC-C-Independent Signaling Pathway
The evidence of the presence of additional receptors and signaling pathways for GPs exist and it is found mostly in the kidney but also in other tissues like intestine. Further research should be done to determine physiological and pathophysiological roles of all GPs signaling pathways in all organic systems that are expressing GPs. The first evidence of existing a GC-C-independent signaling pathway was given in intestine where was shown that localization of GC-C mRNA and binding sites for STa and GPs in the intestine are not identical . Since STa is a more potent activator of GC-C, it is reasonable to believe that it could activate all GPs receptors which is later shown in the kidneys.
Two populations of binding sites for STa in the intestine have been identified: high affinity receptors not coupled to the guanylate cyclase (only 5% of binding sites) and low affinity binding sites coupled to the guanylate cyclase (95% of binding sites) . Those 2 types of binding sites could occur because of regulation of activity of GC-C itself or could present two different receptor types for GPs. Furthermore, GC-C-independent binding sites are located at the basolateral membrane of colonocytes , and those receptors and signaling pathways are still not identified. GC-C-deficient mice are resistant to intestinal secretion produced by STa [93–95]; however, 10% of the STa intestinal binding sites are still present possibly involving Ca2+ signaling pathway with activation of PKC [96, 97].
Necessity of further research for GC-C-independent signaling pathway for GP became more evident when renal effects were still observed in GC-C-deficient mice . GN, UGN, and STa still change membrane potential via changes in membrane conductances of principal cells in isolated cortical collecting ducts of GC-C-deficient mice . G-protein coupled receptor which activates phospholipase A2 was suggested to be a part of cGMP-independent signaling pathway in the mouse and human kidney [98, 99]. After activation of this receptor, intracellular concentration of arachidonic acid increased and changed cell conductances for ions which could lead to natriuresis, kaliuresis, and diureis present in GC-C-deficient mice. Additional signaling pathway is investigated in more detail in different parts of mouse and human kidney nephron segments (see later). Furthermore, GC-C knock-out animals have normal blood pressure. If the GC-C is the only receptor for GPs, UGN-deficient mice should have the normal blood pressure as well which is not the case. Surprisingly, UGN-deficient mice are developing hypertension [100, 101], suggesting the effects of UGN on blood pressure via GC-C-independent signaling pathway. Further research should be done to investigate the importance of GC-C-independent signaling pathway in physiology and pathophysiology in extrarenal tissues and blood pressure regulation.
6. Signaling Pathways of Guanylin Peptides in the Kidney
The main physiological function of GP is to increase salt excretion via kidneys after increased per os intake. However, the effects of the GN and UGN on the kidney nephron segments are slightly different assuming more important physiological role of UGN in maintaining sodium homeostasis. Humans consuming the diet with high amount of salt (10 g/day) excrete more UGN in the urine compared to people at low-salt diet (7 g/day) . In rats on high-salt diet, also increased excretion of UGN as well as cGMP in the urine compared to normally fed animals, suggesting involvement of cGMP signaling pathway in UGN action in the kidney . Furthermore, in UGN-deficient mice natriuresis produced by oral salt load is decreased .
GN has mostly kaliuretic effects in the kidneys; therefore, it was reasonable to believe that GN could play a significant role in potassium secretion after increased dietary potassium intake. Recently, Oh et al. showed that GN and UGN are not involved in intestinal sensing of dietary potassium intake and still unknown hormones stimulate kidney potassium excretion due to increased potassium intake . As can be expected by structure containing 3 disulfide bonds (Figure 1), STa effects in the kidneys are more pronounced compared to GPs as it is shown for intestine obviously activating all signaling pathways present [21, 61].
The action of the GPs could be produced by the intestine with distant endocrine effects on the kidneys and/or paracrine produced locally by the kidney itself. Recent research implicates paracrine effects of GP in the kidney. UGN but not GN kidney expression increases after increased oral salt load. Paracrine production of GP in the kidney is due to still unknown linkage mechanism between intestine and kidney. Kuhn’s laboratory suggested that renal UGN expression is influenced by renal hypertonicity but not by intestinal sensing of salt intake. Cultured murine M-1 cells, cells with properties of cortical collecting duct cells, are showing UGN but not GN expression. UGN expression increases when M-1 cells were put in hypertonic conditions (using hypertonic NaCl solution or mannitol). Further investigations should be done to clarify how increased intestinal sodium load increases UGN expression in the kidney .
Similar to the difference in the axial expression along the intestine (Figure 2), GN and UGN are not expressed equally along the different nephron segments suggesting the similarity in paracrine function between intestine and kidney. mRNA for GN is more expressed in the collecting duct (distal nephron segments), in analogy to GN expression in the colon while mRNA for UGN is present mostly in the proximal tubule, again comparable to the higher expression in proximal intestine (Figure 6) . Goy’s laboratory recently found pro-UGN (the uroguanylin precursor) in distal nephron segments with more pronounced natriuretic effects compared to UGN itself, but they failed to show expression of GC-C in the kidney [104, 105].
Expression of GC-C in the kidney is still controversial. Like in intestine, localization of mRNA for GC-C differs from binding site for STa in the kidney. Potthast et al. showed the expression of GC-C in glomeruli and proximal tubules but not in Henle’s loop and cortical collecting ducts [20, 21, 98]. Exact localization of GC-C is still not known because Carrithers et al. localized GC-C in all parts of rat nephron while Goy’s laboratory failed to show the expression of GC-C in the kidney [105, 106]. From other members of GC-C signaling pathway of GP, PKG II is also expressed in the kidneys. mRNA for PKG II is located in all nephron segments with the highest expression in glomeruli and proximal tubules where the GC-C is also expressed the most [20, 106]. However, the involvement of cGMP and GC-C in the signaling pathway of GPs in proximal tubule cells is obviously not present in the effects of GPs described in GC-C-deficient mice, and GC-C-independent signaling pathway in the kidneys was discovered.
Even the GPs are expressed in different parts of the nephron segments, the most effects of GP are mostly investigated in proximal tubules and collecting duct. Since GPs increase the secretion of sodium, potassium, and water in the kidney without changes in glomerular filtration rate or renal blood flow, the effects of GPs in glomeruli are still unknown.
7. Signaling Pathways of Guanylin Peptides in the Proximal Tubules
The first discovered localization of GPs action is proximal tubule. Proximal tubule cells are specific for their massive ion and water transport. Each day proximal tubules reabsorb 120 L of filtrated water, 65% filtrated sodium, potassium and chloride, and almost all filtrated bicarbonate. Small changes in proximal tubule transport will lead to massive changes in final urine.
Binding sites for GN, UGN, and STa are located at opossum and human proximal tubule cells [69, 70, 107, 108]. In rat proximal tubules, binding sites for STa are found at apical and basolateral cell membranes as well as in basolateral cell membrane of Henle’s loop and medullar collecting duct cells . The possible physiological role for receptors for GPs located at basolateral side of kidney nephron segments is not clear yet. GPs increase intracellular cGMP concentration in a proximal tubule cell line of opossum kidney (OK cells), in kangaroo proximal tubule cells (PtK-2 cells), and in an immortalized human proximal tubule cell line (IHKE1) [21, 68, 77, 110].
Proximal tubule is responsible for more than 90% of filtrated bicarbonate reabsorption. For each hydrogen ion transported via apical membrane, one bicarbonate is reabsorbed back into peritubular capillaries. UGN inhibits the activity of Na+/H+ exchanger isoform 3 (NHE3) located at the apical membrane which decreases the secretion of hydrogen ions and therefore decreases the reabsorption of bicarbonate. UGN inhibits NHE3 activity via cGMP followed by PKG activation and cAMP followed by PKA activation, both of which phosphorylate NHE3 already located at apical membrane of the cells. UGN also reduces NHE3 surface expression . Recently discovered renoguanylin (eel isoform: A D L C E I C A F A A C T G C L) also inhibits hydrogen transport at the apical membrane of proximal tubules in the rat kidneys. Renoguanylin inhibits NHE as well as H+-ATPase and is therefore involved in the regulation of hydrogen and bicarbonate transport as other guanylin peptides . Human isoform of renoguanylin is not discovered yet.
GP regulate not only transport of hydrogen and bicarbonate in proximal tubules, as shown previusly, also change sodium and potassium conductances and electrogenic electrolyte transport in IHKE-1 cells which are a human proximal tubule cell line. GPs are reaching the receptors located at apical membrane of those cells. GPs show different effects in the kidney, UGN mostly causing natriuresis while GN kaliuresis; it was reasonable to expect that the effects on those hormones on proximal tubule cell line differ as well. GN mostly activates cGMP-dependent signaling pathway. Since GPs increase excretion in the urine as well as cGMP due to high-salt diet which is in contrast to still existing effects of GPs in GC-C-deficient mice, another guanylate cyclase could play a role as receptor for GPs in proximal tubules. Guanylate cyclase present in opossum kidney (OK-GC) has a 92–95% identity in the catalytic domain but only 55–58% identity in ligand-binding domain compared with rat, pig, and human GC-C. Human isoform of this still unidentified receptor could play a possible role in cGMP-dependent but GC-C-independent signaling pathway of GPs . In IHKE-1 cells, UGN and STa activate both cGMP-dependent and cGMP independent signaling pathway. UGN also activates both signaling pathway in pig proximal tubule cell line (LLC-PK1). Which signaling pathway will be activated depends on concentrations of the hormone and pH. As it was shown for GC-C in intestine (Figure 3), in proximal tubule cells UGN activates GC-C and depolarized cells (as well as cGMP) at pH 5.5. When the pH values change to 8.0, we can assume that affinity of GC-C for UGN decrease and other GC-C-independent signaling pathway could be more pronounced which leads to UGN-dependent hyperpolarization of the cells (Figure 7). Could this switch in signaling pathways due to pH differance play any physiological role in regulation of sodium, hydrogen, bicarbonate transport versus potassium transport needs to be established.
Preincubation of IHKE-1 cells with pertussis toxin (PT), an inhibitor of G-protein coupled receptors, has no effect on depolarizations neither on cGMP accumulation caused by GPs. However, hyperpolarization caused by UGN is inhibited by PT suggesting that the second receptor activated by UGN and probably also by STa is a PT-sensitive G-protein coupled receptor .
8. Signaling Pathways of Guanylin Peptides in the Collecting Ducts
Final hormonal regulation of renal electrolyte and water homeostasis takes place in the collecting duct (CD). They have at least 2 types of the cells: principal cells which are responsible for K+ secretion (ROMK channels), Na+, and water reabsorption (ENaC and aquaporins 2, 3, and 4, resp.) and intercalated cells responsible for K+ reabsorption via ATPases. We already discussed the importance of sodium regulation, but regulation of potassium plasma concentration is even more important because of its serious consequences on heart function in hyperkalemic conditions. There are numerous mechanisms for potassium homeostasis regulation by the kidney from aldosterone to direct regulation by plasmatic potassium concentration. Due to aldosterone activation of Na+/K+ ATPase and increased apical membrane conductances for sodium (ENaC) and potassium (ROMK) of principal cells, sodium is reabsorbed in the blood and potassium is secreted in the tubular lumen. To be able to reabsorb potassium, intercalated cells have H+/K+-ATPase at the apical membrane which secrete hydrogen ions and reabsorb potassium. Since GPs at the same time induce natriuresis and kaliuresis, it is reasonable to believe that those hormones regulate water and electrolyte transport in principal cells as well as in intercalated cell of collecting ducts. Since GN showed more pronounced kaliuresis, its physiological importance in potassium homeostasis in contrast to aldosterone is suggested and future research should clarify physiological importance of GN in the kidney.
Collecting ducts are cortical collecting duct (CCD) and medullary collecting duct (MCD). Even the final regulation of electrolyte and especially water transport is located at the end part of the nephron, MCDs; however, most of the research of GPs signaling pathways in the kidney nephron segments was done at CCDs.
8.1. Signaling Pathways of Guanylin Peptides in Principal Cells of CCD
GPs change membrane conductances and therefore membrane voltages of principal cells of wild-type mice and human CCD. The same results are presented for principal cells isolated from CCDs of GC-C-deficient mice which are in line with the observation that GC-C-deficient mice still exert natriuresis, kaliuresis, and diuresis upon GPs infusion [5, 98, 99]. The source of UGN reaching the lumen of the collecting duct is filtrated from the blood where secreted by intestine and/or from secretion by proximal tubule cells . It looks like the GN present in lumen of CDs could be secreted only by local cells since GN is degradated with chymotrypsin which is located in all parts of the nephron, and mRNA for GN is most present in the cells of collecting ducts. Since UGN, in contrast to GN, is resistant to degradation by luminal proteases and probably secreted by proximal tubule where the expression of mRNA for UGN is the highest, UGN will be concentrated along the nephron due to volume reabsorption and will be present in the final urine (Figure 8) .
It is already established that GN and UGN have different effects on the kidney in in vivo experiments. In mouse and human principal cells of cortical collecting ducts, they express slightly different effects which are species specific while differ in mouse and human principal cells.
In mouse principal cells of CCDs, GPs activate receptors located at apical membrane similar to effects of GPs in the intestine. GN mainly depolarized cells while UGN, STa, and membrane permeable cGMP (8 Br cGMP) hyperpolarized cells due to changes in potassium conductances (depolarizations due to a decrease, hyperpolarizations due to an increase in a K+ conductance) suggesting different sensitivities of the two signaling pathways for GPs. However, hyperpolarizations caused by GPs (activation of cGMP-dependent signaling pathway) are still present in principal cells from CCDs isolated from GC-C-deficient mice. In the same guanylate cyclase C-deficient mice, GPs still increase the cGMP concentration in urine, indicating an involvement of another guanylate cyclase than guanylate cyclase C . GC-G is other type of guanylate cyclase present in mouse collecting duct which could be responsible for cGMP- and PKG-dependent signaling pathways of GPs in those cells. It is known that PKG activates Ca2+-dependent K+ channels which could be responsible for PKG-dependent hyperpolarizations caused by GPs. cGMP-independent signaling pathway (depolarizations caused by GPs) involves G-coupled receptor (could be the same as already shown in proximal tubule cell line) which activates phospholipase A2 and release of arachidonic acid. Since arachidonic acid inhibits potassium channels, ROMK, located at apical membrane of principal cells, those channels could be the target protein of cGMP-independent GPs action in principal cells [99, 113].
Recently, the first electrophysiology study of principal cells of human CCDs was performed. Starting membrane potential of human principal cells is not different from starting membrane potential of mouse and rat principal cells which assumes similar potassium conductances between different species. However, only one signaling pathway for GPs is present in human principal cells. GPs depolarized while again membrane permeable analog of cGMP hyperpolarized cells clearly identify signaling pathway for GPs as GC-C and cGMP independent. Ca2+ and PKC are suggested as a possible additional and cGMP-independent signaling pathway for GPs in the intestine but that was not the case for principal cells because the GPs are not changing intracellular concentration of calcium. As it is shown for mouse, depolarizations of human principal cells caused by GPs are due to inhibition of potassium conductances, which consequently leads to reduction of driving force for sodium reabsorption and therefore possible natriuresis. The remaining question is if GPs could inhibit potassium reabsorption in intercalated cells and therefore induce kaliuresis as well. However, ROMK-deficient mice show natriuresis, kaliuresis, and diuresis, a pattern of responses so similar to mice stimulated with GPs which is still not fully understood . As it was shown for human principal cells as well as for mouse principal cells, cGMP-independent signaling pathway for GPs actually leads to inhibition of ROMK channels by arachidonic acid therefore, the effects of GPs on kidneys could share the same mechanisms of natriuresis, kaliuresis, and diuresis as is present in ROMK-deficient mice .
Activation of G-protein coupled receptor which leads to activation of PLA2 and increase of intracellular concentration of arachidonic acid is shown by G-protein coupled receptor 14 (GPR14) . Two types of the cells, human embryonic cell line (HEK283) cells and Chinese hamster ovary (CHO) cells overexpressing GPR14 receptor, showed different effects of GPs. Only HEK293 cells obviously express all necessary proteins which makes them suitable for this kind of studies in contrast to CHO cells suggesting the importance of expression system in investigating possible receptors for GPs. Depolarization of HEK293-GPR14 cells induced by GPs is higher compared to WT cells . Whether this is the G-protein coupled receptor activated by GPs actions in the different mouse and human nephron segments needs to be further investigated.
8.2. Signaling Pathways of Guanylin Peptides in Intercalated Cells of CCD
It is far less known about signaling pathway of GPs in the intercalated cells. Resent work from Zelinkovic’s laboratory suggested the effects of UGN on exchanger, pendrin, located in intercalated cells . In apical membrane of intercalated cells type non-A, non-B of CCD, pendrin, functions as exchanger where it is involved in bicarbonate transport. Pendrin is proposed to be involved in the functions of aldosterone and angiotensin II. Even UGN originally works opposite to those hormones, it could regulate the expression of this anion exchanger. Physiological function of this regulation needs more clarification.
8.3. Signaling Pathways of Guanylin Peptides in MCD
It is less known about the function of GPs in the last part of the nephron, medullary CD. GPs decrease the cell volume and increase the luminal space which suggests secretion of water and consequently diuresis ; however, GPs do not change water permeability in inner medullary CD cells .
9. Cellular Effects of Guanylin Peptides in Other Organs
Patients with cystic fibrosis have pathological changes in water and electrolyte transport in the pancreas, the liver, the lung, and the intestine. It might be speculated that GPs are also involved in the physiology of those organs.
GPs and parts of their signaling pathway are present in the pancreas. mRNA for GC-C and UGN are detected in the cells of the exocrine part of the pancreas, and GN increases intracellular cGMP via GC-C in a human pancreatic cell line [118–120]. In pancreas, GPs could be involved in a very demanding bicarbonate secretion necessary for acidity neutralization in duodenum.
In the liver, GN is located in the epithelial cells of bile ducts and of the gallbladder. Other members of GC-C signaling pathways of GPs (GC-C, PKG II, CFTR, and anion exchanger Slc4a2) are located at the apical membrane of the same cells suggesting physiological role of GN in production of hepatic and cystic bile via regulation of water and electrolyte transport by paracrine signaling pathway . mRNA for GC-C is present in fetuses and newborn rats, after partial hepatectomies, and during liver regeneration suggesting an additional role of GPs in those conditions [79, 94, 122, 123].
Lungs are one of the most damaged organs in cystic fibrosis. In healthy individuals, GN is secreted by airways where it activates a well-known GC-C signaling pathway and leads to CFTR activation [70, 78, 79, 124, 125]. Furthermore, GPs relax tracheal smooth muscle cells and mucus production in large and small airways, which suggests UGN as a new treatment of asthma [126, 127].
GPs and parts of the GC-C-dependent signaling pathway are also found in sweat glands, the adrenal medulla, and the male reproductive system [128–130]. Recently it was discovered that UGN relaxes human corpus cavernosus and could be used in the treatment of erectile dysfunction . Even the appetite is proposed to be regulated by circulatory pro-UGN secreted from the intestine and binding to GC-C in hypothalamus .
According to this limited information on the effects of GPs on various organs, the GC-C-dependent signaling pathway seems to be the predominant signaling pathway in most organs and only in the kidney does the signaling involve different receptors and signaling mechanisms. Like it is shown for the regulation of blood pressure by UGH, further studies are necessary to determine the possible physiological function of GC-C-independent signaling pathways of GPs in extrarenal tissues.
10. Guanylin Peptides in Pathophysiology
The most investigated pathological conditions which are involving GPs are intestinal tumors. GPs are less expressed in colon adenocarcinoma, adenoma, and intestine polyps in mouse and human compared to healthy individuals suggesting involvement of GPs in the development of intestinal tumors [133–135]. Indeed, GPs regulate proliferation and differentiation, prolong the cell cycle, and induce apoptosis of T84, CaCo-2 cells, and mouse intestinal cells, and oral application of UGN leads to a decrease in the number and size of polyps in mice that develop intestinal polyposis [133, 136–140]. Like UGN, nonsteroidal antiinflammatory drug as well present their anticancer effects via increase in cellular levels of cGMP [135, 141, 142]. Among other factors, like differences in type and food processing, increased levels of cGMP induced by frequent diarrhea in third world countries are presumed to be protective against intestine cancers. Furthermore, ectopic expression of GC-C could be used as marker for development of metastasis in lymphatic system of esophageal, stomach, and colon cancer [143–146].
Cystic fibrosis (CF) is a genetic disease caused by mutations of cystic fibrosis transmembrane conductance regulator (CFTR) mostly affecting lungs, pancreas, liver, and intestine. CFTR is chloride channel which regulates membrane conductances of the affected cells for, as far as we know, chloride, sodium, and bicarbonate; reduced amount of electrolytes in lumen results in less water secretion and production of thick mucus which blocks airways in the lung, pancreatic ducts, and bile ducts in the liver and causes meconium ileus. This intestinal obstruction in the newborn could be seen in CF patients, is connected to mutations of the gene for guanylate cyclase C . Furthermore, GPs still stimulate bicarbonate secretion in CFTR-deficient mice, and recently Slc26a4 (pendrin) was suggested as target for UGN-dependent chloride transport in intercalated cells of kidney cortical collecting duct suggesting the existence of CFTR-independent signaling pathway for GPs in cystic fibrosis patients . How GPs help dilute thick mucous secretion in the intestine via GC-C-dependent signaling but CFTR-independent signaling pathway needs to be established. Although life span of patients suffering from CF is significantly increased, the therapy is still symptomatic. Since the GPs colocalize with CFTR, future research should be done to determine whether GPs regulation of water and electrolyte transport has any physiological effect on the lung, pancreas, and intestine of CF patients (via GC-C-independent signaling pathways) and could GPs effects on ion transport be used as a new therapy approach in patients with cystic fibrosis.
GPs are also involved in different kidney diseases. Concentrations in plasma GPs increase in patients with chronic renal failure and glomerulonephritis and in patients on hemodialysis [27, 29, 30, 40, 148]. In patients with nephritic syndrome, UGN plasma concentration was higher and urinary concentration was lower compared with values in healthy volunteers possibly because kidney is damaged and it has reduced capability to metabolize and excrete GPs . Recently, in experimental nephrotic syndrome, changes in UGN concentrations in urine and plasma corresponded to changes in Na+ excretion; therefore, UGN could be used as natriuretic peptide in nephritic syndrome [149, 150].
GPs are well known as intestinal natriuretic peptides with well-established function in the intestine and the kidneys. GN and UGN regulate electrolyte and water transport in the intestine and cause kaliuresis, natriuresis, and diuresis in the kidney. After a salty meal, GPs decrease sodium reabsorption from the intestine and induce sodium secretion by the kidneys and therefore prevent postprandial hypernatraemia which could occur.
The main signaling pathway for GPs includes GC-C and increase intracellular concentration of cGMP followed by activation of PKG II, inhibition of Na+/H+ exchange, and CFTR activation. Additional GC-C-independent signaling pathway exists in intestine but is still not well understood; however, this signaling pathway is more investigated in the kidney, and it is suggested to be more important for GPs action in the kidney than GC-C-dependent signaling pathway. It is established that other signaling pathways involve G-coupled receptors (probably GPR14), the molecular identity receptors for GPs in the kidney and other extrarenal tissues remain to be determined.
We have known that GPs and their signaling pathways exist in other organs like liver, pancreas, lung, sweat glands, and male reproductive system and they are involved in different pathological conditions like cystic fibrosis, asthma, intestinal tumors, and kidney and heart failure. Future research should investigate the importance of GC-C-independent signaling pathways in extrarenal tissues and determine new treatments for pathological conditions.
- R. J. Lennane, W. S. Peart, R. M. Carey, and J. Shaw, “A comparison of natriuresis after oral and intravenous sodium loading in sodium depleted rabbits: evidence for a gastrointestinal or portal monitor of sodium intake,” Clinical Science and Molecular Medicine, vol. 49, no. 5, pp. 433–436, 1975.
- T. Kita, K. Kitamura, J. Sakata, and T. Eto, “Marked increase of guanylin secretion in response to salt loading in the rat small intestine,” American Journal of Physiology, vol. 277, no. 5, pp. G960–G966, 1999.
- Z. Li, J. W. Knowles, D. Goyeau et al., “Low salt intake down-regulates the guanylin signaling pathway in rat distal colon,” Gastroenterology, vol. 111, no. 6, pp. 1714–1721, 1996.
- R. N. Greenberg, M. Hill, J. Crytzer et al., “Comparison of effects of uroguanylin, guanylin, and Escherichia coli heat-stable enterotoxin STa in mouse intestine and kidney: evidence that uroguanylin is an intestinal natriuretic hormone,” Journal of Investigative Medicine, vol. 45, no. 5, pp. 276–283, 1997.
- S. L. Carrithers, C. E. Ott, M. J. Hill et al., “Guanylin and uroguanylin induce natriuresis in mice lacking guanylyl cyclase-C receptor,” Kidney International, vol. 65, no. 1, pp. 40–53, 2004.
- M. C. Fonteles, R. N. Greenberg, H. S. A. Monteiro, M. G. Currie, and L. R. Forte, “Natriuretic and kaliuretic activities of guanylin and uroguanylin in the isolated perfused rat kidney,” American Journal of Physiology, vol. 275, no. 2, pp. F191–F197, 1998.
- M. G. Currie, K. F. Fok, J. Kato et al., “Guanylin: an endogenous activator of intestinal guanylate cyclase,” Proceedings of the National Academy of Sciences of the United States of America, vol. 89, no. 3, pp. 947–951, 1992.
- F. K. Hamra, L. R. Forte, S. L. Eber et al., “Uroguanylin: structure and activity of a second endogenous peptide that stimulates intestinal guanylate cyclase,” Proceedings of the National Academy of Sciences of the United States of America, vol. 90, no. 22, pp. 10464–10468, 1993.
- L. R. Forte, S. L. Eber, X. Fan et al., “Lymphoguanylin: cloning and characterization of a unique member of the guanylin peptide family,” Endocrinology, vol. 140, no. 4, pp. 1800–1806, 1999.
- S. Yuge, K. Inoue, S. Hyodo, and Y. Takei, “A novel guanylin family (guanylin, uroguanylin, and renoguanylin) in eels: possible osmoregulatory hormones in intestine and kidney,” Journal of Biological Chemistry, vol. 278, no. 25, pp. 22726–22733, 2003.
- S. Schulz, “Targeted gene disruption in the development of mouse models to elucidate the role of receptor guanylyl cyclase signaling pathways in physiological function,” Methods, vol. 19, no. 4, pp. 551–558, 1999.
- O. Hill, M. Kuhn, H. D. Zucht et al., “Analysis of the human guanylin gene and the processing and cellular localization of the peptide,” Proceedings of the National Academy of Sciences of the United States of America, vol. 92, no. 6, pp. 2046–2050, 1995.
- H. J. Mägert, M. Reinecke, I. David et al., “Uroguanylin: gene structure, expression, processing as a peptide hormone, and co-storage with somatostatin in gastrointestinal D-cells,” Regulatory Peptides, vol. 73, no. 3, pp. 165–176, 1998.
- F. J. de Sauvage, S. Keshav, W. J. Kuang, N. Gillett, W. Henzel, and D. V. Goeddel, “Precursor structure, expression, and tissue distribution of human guanylin,” Proceedings of the National Academy of Sciences of the United States of America, vol. 89, no. 19, pp. 9089–9093, 1992.
- M. Miyazato, M. Nakazato, S. Matsukura, K. Kangawa, and H. Matsuo, “Uroguanylin gene expression in the alimentary tract and extra-gastrointestinal tissues,” FEBS Letters, vol. 398, no. 2-3, pp. 170–174, 1996.
- T. Kita, C. E. Smith, K. F. Fok et al., “Characterization of human uroguanylin: a member of the guanylin peptide family,” American Journal of Physiology, vol. 266, no. 2, pp. F342–F348, 1994.
- R. Hess, M. Kuhn, P. Schulz-Knappe et al., “GCAP-II: isolation and characterization of the circulating form of human uroguanylin,” FEBS Letters, vol. 374, no. 1, pp. 34–38, 1995.
- T. L. Whitaker, D. P. Witte, M. C. Scott, and M. B. Cohen, “Uroguanylin and guanylin: distinct but overlapping patterns of messenger RNA expression in mouse intestine,” Gastroenterology, vol. 113, no. 3, pp. 1000–1006, 1997.
- F. K. Hamra, S. L. Eber, D. T. Chin, M. G. Currie, and L. R. Forte, “Regulation of intestinal uroguanylin/guanylin receptor-mediated responses by mucosal acidity,” Proceedings of the National Academy of Sciences of the United States of America, vol. 94, no. 6, pp. 2705–2710, 1997.
- R. Potthast, E. Ehler, L. A. Scheving, A. Sindic, E. Schlatter, and M. Kuhn, “High salt intake increases uroguanylin expression in mouse kidney,” Endocrinology, vol. 142, no. 7, pp. 3087–3097, 2001.
- A. Sindiće, C. Basoglu, A. Çerçi et al., “Guanylin, uroguanylin, and heat-stable euterotoxin activate guanylate cyclase C and/or a pertussis toxin-sensitive G protein in human proximal tubule cells,” Journal of Biological Chemistry, vol. 277, no. 20, pp. 17758–17764, 2002.
- K. Nokihara, V. Wray, E. Ando, S. Naruse, and T. Hayakawa, “Synthesis, solution structure, binding activity, and cGMP activation of human guanylin and its disulfide isomer,” Regulatory Peptides, vol. 70, no. 2-3, pp. 111–120, 1997.
- S. Schulz, C. K. Green, P. S. T. Yuen, and D. L. Garbers, “Guanylyl cyclase is a heat-stable enterotoxin receptor,” Cell, vol. 63, no. 5, pp. 941–948, 1990.
- M. Field, L. H. Graf, W. J. Laird, and P. L. Smith, “Heat-stable enterotoxin of Escherichia coli: in vitro effects on guanylate cyclase activity, cyclic GMP concentration, and ion transport in small intestine,” Proceedings of the National Academy of Sciences of the United States of America, vol. 75, no. 6, pp. 2800–2804, 1978.
- J. M. Hughes, F. Murad, B. Chang, and R. L. Guerrant, “Role of cyclic GMP in the action of heat-stable enterotoxin of Escherichia coli,” Nature, vol. 271, no. 5647, pp. 755–756, 1978.
- M. Kuhn, M. Raida, K. Adermann et al., “The circulating bioactive form of human guanylin is a high molecular weight peptide (10.3 kDa),” FEBS Letters, vol. 318, no. 2, pp. 205–209, 1993.
- M. Nakazato, H. Yamaguchi, K. Shiomi et al., “Identification of 10-kDa proguanylin as a major guanylin molecule in human intestine and plasma and its increase in renal insufficiency,” Biochemical and Biophysical Research Communications, vol. 205, no. 3, pp. 1966–1975, 1994.
- H. J. Mägert, O. Hill, H. D. Zucht et al., “Porcine guanylin and uroguanylin: cDNA sequences, deduced amino acid sequences, and biological activity of the chemically synthesized peptides,” Biochemical and Biophysical Research Communications, vol. 259, no. 1, pp. 141–148, 1999.
- H. Kinoshita, S. Fujimoto, M. Nakazato et al., “Urine and plasma levels of uroguanylin and its molecular forms in renal diseases,” Kidney International, vol. 52, no. 4, pp. 1028–1034, 1997.
- M. Nakazato, H. Yamaguchi, H. Kinoshita et al., “Identification of biologically active and inactive human uroguanylins in plasma and urine and their increases in renal insufficiency,” Biochemical and Biophysical Research Communications, vol. 220, no. 3, pp. 586–593, 1996.
- N. G. Moss, R. C. Fellner, X. Qian et al., “Uroguanylin, an intestinal natriuretic peptide, is delivered to the kidney as an unprocessed propeptide,” Endocrinology, vol. 149, no. 9, pp. 4486–4498, 2008.
- X. Qian, N. G. Moss, R. C. Fellner, and M. F. Goy, “Circulating prouroguanylin is processed to its active natriuretic form exclusively within the renal tubules,” Endocrinology, vol. 149, no. 9, pp. 4499–4509, 2008.
- F. K. Hamra, X. Fan, W. J. Krause et al., “Prouroguanylin and proguanylin: purification from colon, structure, and modulation of bioactivity by proteases,” Endocrinology, vol. 137, no. 1, pp. 257–265, 1996.
- F. K. Hamra, W. J. Krause, S. L. Eber et al., “Opossum colonic mucosa contains uroguanylin and guanylin peptides,” American Journal of Physiology, vol. 270, no. 4, pp. G708–G716, 1996.
- M. Arao, T. Yamaguchi, T. Sugimoto, M. Fukase, and K. Chihara, “Characterization of a chymotrypsin-like hydrolytic activity in the opossum kidney cell,” Biochemistry and Cell Biology, vol. 72, no. 3-4, pp. 157–162, 1994.
- M. Miyazato, M. Nakazato, H. Yamaguchi et al., “Cloning and characterization of a cDNA encoding a precursor for human uroguanylin,” Biochemical and Biophysical Research Communications, vol. 219, no. 2, pp. 644–648, 1996.
- Z. Li, A. G. Perkins, M. F. Peters, M. J. Campa, and M. F. Goy, “Purification, cDNA sequence, and tissue distribution of rat uroguanylin,” Regulatory Peptides, vol. 68, no. 1, pp. 45–56, 1997.
- M. Nakazato, H. Yamaguchi, Y. Date et al., “Tissue distribution, cellular source, and structural analysis of rat immunoreactive uroguanylin,” Endocrinology, vol. 139, no. 12, pp. 5247–5254, 1998.
- H. Kinoshita, M. Nakazato, H. Yamaguchi, S. Matsukura, S. Fujimoto, and T. Eto, “Increased plasma guanylin levels in patients with impaired renal function,” Clinical Nephrology, vol. 47, no. 1, pp. 28–32, 1997.
- H. Kinoshita, S. Fujimoto, H. Fukae et al., “Plasma and urine levels of uroguanylin, a new natriuretic peptide, in nephrotic syndrome,” Nephron, vol. 81, no. 2, pp. 160–164, 1999.
- S. Martin, K. Adermann, W. G. Forssmann, and M. Kuhn, “Regulated, side-directed secretion of proguanylin from isolated rat colonic mucosa,” Endocrinology, vol. 140, no. 11, pp. 5022–5029, 1999.
- F. Moro, F. Levenez, E. Nemoz-Gaillard, S. Pellissier, P. Plaisancie, and J. C. Cuber, “Release of guanylin immunoreactivity from the isolated vascularly perfused rat colon,” Endocrinology, vol. 141, no. 7, pp. 2594–2599, 2000.
- Y. Date, M. Nakazato, H. Yamaguchi et al., “Enterochromaffin-like cells, a cellular source of uroguanylin in rat stomach,” Endocrinology, vol. 140, no. 5, pp. 2398–2404, 1999.
- R. K. Blanchard and R. J. Cousins, “Differential display of intestinal mRNAs regulated by dietary zinc,” Proceedings of the National Academy of Sciences of the United States of America, vol. 93, no. 14, pp. 6863–6868, 1996.
- R. K. Blanchard and R. J. Cousins, “Upregulation of rat intestinal uroguanylin mRNA by dietary zinc restriction,” American Journal of Physiology, vol. 272, no. 5, pp. G972–G978, 1997.
- L. Cui, R. K. Blanchard, L. M. Coy, and R. J. Cousins, “Prouroguanylin overproduction and localization in the intestine of zinc-deficient rats,” Journal of Nutrition, vol. 130, no. 11, pp. 2726–2732, 2000.
- R. K. Blanchard and R. J. Cousins, “Regulation of intestinal gene expression by dietary zinc: induction of uroguanylin mRNA by zinc deficiency,” Journal of Nutrition, vol. 130, no. 5, pp. 1393S–1398S, 2000.
- C. Ott, B. Jackson, A. Carvalho, R. Greenberg, and S. Carrithers, “Regulation of intestinal uroguanylin (UGN) expression by dietary salt intake,” The FASEB Journal, vol. 16, p. A472, 2000.
- A. Perkins, M. F. Goy, and Z. Li, “Uroguanylin is expressed by enterochromaffin cells in the rat gastrointestinal tract,” Gastroenterology, vol. 113, no. 3, pp. 1007–1014, 1997.
- Y. Cetin, M. Kuhn, H. Kulaksiz et al., “Enterochromaffin cells of the digestive system: cellular source of guanylin, a guanylate cyclase-activating peptide,” Proceedings of the National Academy of Sciences of the United States of America, vol. 91, no. 8, pp. 2935–2939, 1994.
- R. M. London, W. J. Krause, X. Fan, S. L. Eber, and L. R. Forte, “Signal transduction pathways via guanylin and uroguanylin in stomach and intestine,” American Journal of Physiology, vol. 273, no. 1, pp. G93–G105, 1997.
- R. C. Wiegand, J. Kato, M. D. Huang, K. F. Fok, J. F. Kachur, and M. G. Currie, “Human guanylin: cDNA isolation, structure, and activity,” FEBS Letters, vol. 311, no. 2, pp. 150–154, 1992.
- R. C. Wiegand, J. Kato, and M. G. Currie, “Rat guanylin cDNA: characterization of the precursor of an endogenous activator of intestinal guanylate cyclase,” Biochemical and Biophysical Research Communications, vol. 185, no. 3, pp. 812–817, 1992.
- X. Fan, F. K. Hamra, R. M. London et al., “Structure and activity of uroguanylin and guanylin from the intestine and urine of rats,” American Journal of Physiology, vol. 273, no. 5, pp. E957–E964, 1997.
- J. Rozenfeld, O. Tal, O. Kladnitsky et al., “The pendrin anion exchanger gene is transcriptionally regulated by uroguanylin: a novel enterorenal link,” American Journal of Physiology, vol. 302, no. 5, pp. F614–F624, 2012.
- Z. Li, B. Taylor-Blake, A. R. Light, and M. F. Goy, “Guanylin, an endogenous ligand for C-type guanylate cyclase, is produced by goblet cells in the rat intestine,” Gastroenterology, vol. 109, no. 6, pp. 1863–1875, 1995.
- S. Furuya, S. Naruse, and T. Hayakawa, “Intravenous injection of guanylin induces mucus secretion from goblet cells in rat duodenal crypts,” Anatomy and Embryology, vol. 197, no. 5, pp. 359–367, 1998.
- A. B. Vaandrager, A. G. M. Bot, and H. R. de Jonge, “Guanosine 3′,5′-cyclic monophosphate-dependent protein kinase ii mediates heat-stable enterotoxin-provoked chloride secretion in rat intestine,” Gastroenterology, vol. 112, no. 2, pp. 437–443, 1997.
- A. B. Vaandrager, A. G. M. Bot, P. Ruth, A. Pfeifer, F. Hofmann, and H. R. de Jonge, “Differential role of cyclic GMP-dependent protein kinase II in ion transport in murine small intestine and colon,” Gastroenterology, vol. 118, no. 1, pp. 108–114, 2000.
- A. C. Chao, F. J. de Sauvage, Y. J. Dong, J. A. Wagner, D. V. Goeddel, and P. Gardner, “Activation of intestinal CFTR Cl− channel by heat-stable enterotoxin and guanylin via cAMP-dependent protein kinase,” EMBO Journal, vol. 13, no. 5, pp. 1065–1072, 1994.
- T. P. Dousa, “Cyclic-3′,5′-nucleotide phosphodiesterase isozymes in cell biology and pathophysiology of the kidney,” Kidney International, vol. 55, no. 1, pp. 29–62, 1999.
- K. Fawcus, V. J. Gorton, M. L. Lucas, and G. T. A. McEwan, “Stimulation of three distinct guanylate cyclases induces mucosal surface alkalinisation in rat small intestine in vitro,” Comparative Biochemistry and Physiology A, vol. 118, no. 2, pp. 291–295, 1997.
- R. Toriano, M. Ozu, M. T. Politi, R. A. Dorr, M. A. Curto, and C. Capurro, “Uroguanylin regulates net fluid secretion via the NHE2 isoform of the Na+/H+ exchanger in an intestinal cellular model,” Cellular Physiology and Biochemistry, vol. 28, no. 4, pp. 733–742, 2011.
- N. S. Joo, R. M. London, H. D. Kim, L. R. Forte, and L. L. Clarke, “Regulation of intestinal Cl− and HCO3− secretion by uroguanylin,” American Journal of Physiology, vol. 274, no. 4, pp. G633–G644, 1998.
- A. W. Cuthbert, M. E. Hickman, L. J. MacVinish et al., “Chloride secretion in response to guanylin in colonic epithelia from normal and transgenic cystic fibrosis mice,” British Journal of Pharmacology, vol. 112, no. 1, pp. 31–36, 1994.
- J. L. Goldstein, J. Sahi, M. Bhuva, T. J. Layden, and M. C. Rao, “Escherichia coli heat-stable enterotoxin-mediated colonic Cl− secretion is absent in cystic fibrosis,” Gastroenterology, vol. 107, no. 4, pp. 950–956, 1994.
- X. Y. Tien, T. A. Brasitus, M. A. Kaetzel, J. R. Dedman, and D. J. Nelson, “Activation of the cystic fibrosis transmembrane conductance regulator by cGMP in the human colonic cancer cell line, Caco-2,” Journal of Biological Chemistry, vol. 269, no. 1, pp. 51–54, 1994.
- L. R. Forte, W. J. Krause, and R. H. Freeman, “Receptors and cGMP signalling mechanism for E. coli enterotoxin in opossum kidney,” American Journal of Physiology, vol. 255, no. 5, pp. F1040–F1046, 1988.
- L. R. Forte, W. J. Krause, and R. H. Freeman, “Escherichia coli enterotoxin receptors: localization in opossum kidney, intestine, and testis,” American Journal of Physiology, vol. 257, no. 5, pp. F874–F881, 1989.
- W. J. Krause, R. H. Freeman, and L. R. Fort, “Autoradiographic demonstration of specific binding sites for E. coli enterotoxin in various epithelia of the North American opossum,” Cell and Tissue Research, vol. 260, no. 2, pp. 387–394, 1990.
- J. R. Hirsch, M. Meyer, H. J. Mägert et al., “cGMP-dependent and -independent inhibition of a K+ conductance by natriuretic peptides: molecular and functional studies in human proximal tubule cells,” Journal of the American Society of Nephrology, vol. 10, no. 3, pp. 472–480, 1999.
- J. R. Hirsch, N. Skutta, and E. Schlatter, “Signaling and distribution of NPR-Bi, the human splice form of the natriuretic peptide receptor type B,” American Journal of Physiology, vol. 285, no. 2, pp. F370–F374, 2003.
- N. Basu and S. S. Visweswariah, “Defying the stereotype: non-canonical roles of the Peptide hormones guanylin and uroguanylin,” Frontiers in Endocrinology, vol. 2, p. 14, 2011.
- J. R. Hirsch, M. Kruhøffer, P. Herter, et al., “Cellular localization, membrane distribution, and possible function of guanylyl cyclases A and 1 in collecting ducts of rat,” Cardiovascular Research, vol. 51, no. 3, pp. 553–561, 2001.
- M. Kuhn, C. K. D. Ng, Y. H. Su et al., “Identification of an orphan guanylate cyclase receptor selectively expressed in mouse testis,” Biochemical Journal, vol. 379, no. 2, pp. 385–393, 2004.
- S. Schulz, B. J. Wedel, A. Matthews, and D. L. Garbers, “The cloning and expression of a new guanylyl cyclase orphan receptor,” Journal of Biological Chemistry, vol. 273, no. 2, pp. 1032–1037, 1998.
- X. Fan, Y. Wang, R. M. London et al., “Signaling pathways for guanylin and uroguanylin in the digestive, renal, central nervous, reproductive, and lymphoid systems,” Endocrinology, vol. 138, no. 11, pp. 4636–4648, 1997.
- S. P. Range, E. D. Holland, G. P. Basten, and A. J. Knox, “Regulation of guanosine 3′:5′-cyclic monophosphate in ovine tracheal epithelial cells,” British Journal of Pharmacology, vol. 120, no. 7, pp. 1249–1254, 1997.
- S. Schulz, T. D. Chrisman, and D. L. Garbers, “Cloning and expression of guanylin. Its existence in various mammalian tissues,” Journal of Biological Chemistry, vol. 267, no. 23, pp. 16019–16021, 1992.
- D. W. Laney, E. A. Mann, S. C. Dellon, D. R. Perkins, R. A. Giannella, and M. B. Cohen, “Novel sites for expression of an Escherichia coli heat-stable enterotoxin receptor in the developing rat,” American Journal of Physiology, vol. 263, no. 5, pp. G816–G821, 1992.
- T. Gudermann, B. Nurnberg, and G. Schultz, “Receptors and G proteins as primary components of transmembrane signal transduction—part 1: G-protein-coupled receptors: structure and function,” Journal of Molecular Medicine, vol. 73, no. 2, pp. 51–63, 1995.
- T. Okamoto, T. Katada, Y. Murayama, M. Ui, E. Ogata, and I. Nishimoto, “A simple structure encodes G protein-activating function of the IGF-II/mannose 6-phosphate receptor,” Cell, vol. 62, no. 4, pp. 709–717, 1990.
- K. A. Lucas, G. M. Pitari, S. Kazerounian et al., “Guanylyl cyclases and signaling by cyclic GMP,” Pharmacological Reviews, vol. 52, no. 3, pp. 375–413, 2000.
- A. B. Vaandrager, E. van der Wiel, and H. R. de Jonge, “Heat-stable enterotoxin activation of immunopurified guanylyl cyclase C. Modulation by adenine nucleotides,” Journal of Biological Chemistry, vol. 268, no. 26, pp. 19598–19603, 1993.
- J. K. Crane, M. S. Wehner, E. J. Bolen et al., “Regulation of intestinal guanylate cyclase by the heat-stable enterotoxin of Escherichia coli (STa) and protein kinase C,” Infection and Immunity, vol. 60, no. 12, pp. 5004–5012, 1992.
- J. K. Crane and K. L. Shanks, “Phosphorylation and activation of the intestinal guanylyl cyclase receptor for Escherichia coli heat-stable toxin by protein kinase C,” Molecular and Cellular Biochemistry, vol. 165, no. 2, pp. 111–120, 1996.
- A. Wada, M. Hasegawa, K. Matsumoto et al., “The significance of Ser1029 of the heat-stable enterotoxin receptor (STaR): relation of STa-mediated guanylyl cyclase activation and signaling by phorbol myristate acetate,” FEBS Letters, vol. 384, no. 1, pp. 75–77, 1996.
- N. Roy, M. R. Guruprasad, P. Kondaiah, E. A. Mann, R. A. Giannella, and S. S. Visweswariah, “Protein kinase C regulates transcription of the human guanylate cyclase C gene,” European Journal of Biochemistry, vol. 268, no. 7, pp. 2160–2171, 2001.
- R. Bhandari, K. Suguna, and S. S. Visweswariah, “Guanylyl cyclase C receptor: regulation of catalytic activity by ATP,” Bioscience Reports, vol. 19, no. 3, pp. 179–188, 1999.
- X. Qian, S. Prabhakar, A. Nandi, S. S. Visweswariah, and M. F. Goy, “Expression of GC-C, a receptor-guanylate cyclase, and its endogenous ligands uroguanylin and guanylin along the rostrocaudal axis of the intestine,” Endocrinology, vol. 141, no. 9, pp. 3210–3224, 2000.
- M. R. Crane, M. Hugues, P. D. O'Hanley, and S. A. Waldman, “Identification of two affinity states of low affinity receptors for Escherichia coli heat-stable enterotoxin: correlation of occupation of lower affinity state with guanylate cyclase activation,” Molecular Pharmacology, vol. 41, no. 6, pp. 1073–1080, 1992.
- F. Albano, T. Brasitus, E. A. Mann, A. Guarino, and R. A. Giannella, “Colonocyte basolateral membranes contain Escherichia coli heat-stable enterotoxin receptors,” Biochemical and Biophysical Research Communications, vol. 284, no. 2, pp. 331–334, 2001.
- E. A. Mann, M. L. Jump, J. Wu, E. Yee, and R. A. Giannella, “Mice lacking the guanylyl cyclase C receptor are resistant to STa-induced intestinal secretion,” Biochemical and Biophysical Research Communications, vol. 239, no. 2, pp. 463–466, 1997.
- S. Schulz, M. J. Lopez, M. Kuhn, and D. L. Garbers, “Disruption of the guanylyl cyclase-C gene leads to a paradoxical phenotype of viable but heat-stable enterotoxin-resistant mice,” Journal of Clinical Investigation, vol. 100, no. 6, pp. 1590–1595, 1997.
- A. N. Charney, R. W. Egnor, J. T. Alexander-Chacko, V. Zaharia, E. A. Mann, and R. A. Giannella, “Effect of E. coli heat-stable enterotoxin on colonic transport in guanylyl cyclase C receptor-deficient mice,” American Journal of Physiology, vol. 280, no. 2, pp. G216–G221, 2001.
- U. Ganguly, A. G. Chaudhury, A. Basu, and P. C. Sen, “STa-induced translocation of protein kinase C from cytosol to membrane in rat enterocytes,” FEMS Microbiology Letters, vol. 204, no. 1, pp. 65–69, 2001.
- C. S. Weikel, C. L. Spann, C. P. Chambers, J. K. Crane, J. Linden, and E. L. Hewlett, “Phorbol esters enhance the cyclic GMP response of T84 cells to the heat-stable enterotoxin of Escherichia coli (STa),” Infection and Immunity, vol. 58, no. 5, pp. 1402–1407, 1990.
- A. Sindić, J. R. Hirsch, A. Velic, H. Piechota, and E. Schlatter, “Guanylin and uroguanylin regulate electrolyte transport in isolated human cortical collecting ducts,” Kidney International, vol. 67, no. 4, pp. 1420–1427, 2005.
- A. Sindić, A. Velic, C. Başoglu et al., “Uroguanylin and guanylin regulate transport of mouse cortical collecting duct independent of guanylate cyclase C,” Kidney International, vol. 68, no. 3, pp. 1008–1017, 2005.
- J. N. Lorenz, M. Nieman, J. Sabo et al., “Uroguanylin knockout mice have increased blood pressure and impaired natriuretic response to enteral NaCl load,” Journal of Clinical Investigation, vol. 112, no. 8, pp. 1244–1254, 2003.
- M. Kuhn, “Function and dysfunction of mammalian membrane guanylyl cyclase receptors: lessons from genetic mouse models and implications for human diseases,” Handbook of Experimental Pharmacology, vol. 191, pp. 47–69, 2009.
- H. Fukae, H. Kinoshita, S. Fujimoto, T. Kita, M. Nakazato, and T. Eto, “Changes in urinary levels and renal expression of uroguanylin on low or high salt diets in rats,” Nephron, vol. 92, no. 2, pp. 373–378, 2002.
- K. S. Oh, Y. T. Oh, S. W. Kim, T. Kita, I. Kang, and J. H. Youn, “Gut sensing of dietary K+ intake increases renal K +excretion,” American Journal of Physiology, vol. 301, no. 2, pp. R421–R429, 2011.
- N. G. Moss, D. A. Riguera, R. C. Fellner, C. Cazzolla, and M. F. Goy, “Natriuretic and antikaliuretic effects of uroguanylin and prouroguanylin in the rat,” American Journal of Physiology, vol. 299, no. 6, pp. F1433–F1442, 2010.
- X. Qian, N. G. Moss, R. C. Fellner, B. Taylor-Blake, and M. F. Goy, “The rat kidney contains high levels of prouroguanylin (the uroguanylin precursor) but does not express GC-C (the enteric uroguanylin receptor),” American Journal of Physiology, vol. 300, no. 2, pp. F561–F573, 2011.
- S. L. Carrithers, B. Taylor, W. Y. Cai et al., “Guanylyl cyclase-C receptor mRNA distribution along the rat nephron,” Regulatory Peptides, vol. 95, no. 1–3, pp. 65–74, 2000.
- A. A. White, W. J. Krause, J. T. Turner, and L. R. Forte, “Opossum kidney contains a functional receptor for the Escherichia coli heat-stable enterotoxin,” Biochemical and Biophysical Research Communications, vol. 159, no. 1, pp. 363–367, 1989.
- S. Fujimoto, H. Kinoshita, S. Hara, M. Nakazato, S. Hisanaga, and T. Eto, “Immunohistochemical localization of uroguanylin in the human kidney,” Nephron, vol. 84, no. 1, pp. 88–89, 2000.
- S. Furuya, S. Naruse, E. Ando, K. Nokihara, and T. Hayakawa, “Effect and distribution of intravenously injected 125I-guanylin in rat kidney examined by high-resolution light microscopic radioautography,” Anatomy and Embryology, vol. 196, no. 3, pp. 185–193, 1997.
- R. M. London, S. L. Eber, S. S. Visweswariah, W. J. Krause, and L. R. Forte, “Structure and activity of OK-GC: a kidney receptor guanylate cyclase activated by guanylin peptides,” American Journal of Physiology, vol. 276, no. 6, pp. F882–F891, 1999.
- L. M. A. Lessa, L. R. Carraro-Lacroix, R. O. Crajoinas et al., “Mechanisms underlying the inhibitory effects of uroguanylin on NHE3 transport activity in renal proximal tubule,” American Journal of Physiology, vol. 303, no. 10, pp. F1399–F1408, 2012.
- L. M. A. Lessa, J. B. O. Amorim, M. C. Fonteles, and G. Malnic, “Effect of renoguanylin on hydrogen/bicarbonate ion transport in rat renal tubules,” Regulatory Peptides, vol. 157, no. 1–3, pp. 37–43, 2009.
- C. M. Macica, Y. Yang, S. C. Hebert, and W. H. Wang, “Arachidonic acid inhibits activity of cloned renal K+ channel, ROMK1,” American Journal of Physiology, vol. 271, no. 3, pp. F588–F594, 1996.
- M. Lu, T. Wang, Q. Yan et al., “Absence of small conductance K+ channel (SK) activity in apical membranes of thick ascending limb and cortical collecting duct in ROMK (Bartter's) knockout mice,” Journal of Biological Chemistry, vol. 277, no. 40, pp. 37881–37887, 2002.
- P. Ziltener, C. Mueller, B. Haenig, M. W. Scherz, and O. Nayler, “Urotensin II mediates ERK1/2 phosphorylation and proliferation in GPR14-transfected cell lines,” Journal of Receptors and Signal Transduction, vol. 22, no. 1–4, pp. 155–168, 2002.
- U. Lehner, A. Velić, R. Schroter, E. Schlatter, and A. Sindić, “Ligands and signaling of the G-protein-coupled receptor GPR14, expressed in human kidney cells,” Cellular Physiology and Biochemistry, vol. 20, no. 1–4, pp. 181–192, 2007.
- J. Klokkers, P. Langehanenberg, B. Kemper et al., “Atrial natriuretic peptide and nitric oxide signaling antagonizes vasopressin-mediated water permeability in inner medullary collecting duct cells,” American Journal of Physiology, vol. 297, no. 3, pp. F693–F703, 2009.
- M. John, B. Wiedenmann, M. Kruhoffer et al., “Guanylin stimulates regulated secretion from human neuroendocrine pancreatic cells,” Gastroenterology, vol. 114, no. 4, pp. 791–797, 1998.
- H. Kulaksiz, A. Schmid, M. Hönscheid, R. Eissele, J. Klempnauer, and Y. Cetin, “Guanylin in the human pancreas: a novel luminocrine regulatory pathway of electrolyte secretion via cGMP and CFTR in the ductal system,” Histochemistry and Cell Biology, vol. 115, no. 2, pp. 131–145, 2001.
- H. Kulaksiz and Y. Cetin, “Uroguanylin and guanylate cyclase C in the human pancreas: expression and mutuality of ligand/receptor localization as indicators of intracellular paracrine signaling pathways,” Journal of Endocrinology, vol. 170, no. 1, pp. 267–275, 2001.
- K. Schwabe and Y. Cetin, “Guanylin and functional coupling proteins in the hepatobiliary system of rat and guinea pig,” Histochemistry and Cell Biology, vol. 137, no. 5, pp. 589–597, 2012.
- L. A. Scheving and W. E. Russell, “Guanylyl cyclase C is up-regulated by nonparenchymal cells and hepatocytes in regenerating rat liver,” Cancer Research, vol. 56, no. 22, pp. 5186–5191, 1996.
- E. A. Mann, K. Shanmukhappa, and M. B. Cohen, “Lack of guanylate cyclase C results in increased mortality in mice following liver injury,” BMC Gastroenterology, vol. 10, article 86, 2010.
- Y. Cetin, H. Kulaksiz, P. Redecker et al., “Bronchiolar nonciliated secretory (Clara) cells: source of guanylin in the mammalian lung,” Proceedings of the National Academy of Sciences of the United States of America, vol. 92, no. 13, pp. 5925–5929, 1995.
- Z. H. Zhang, F. Jow, R. Numann, and J. Hinson, “The airway-epithelium: a novel site of action by guanylin,” Biochemical and Biophysical Research Communications, vol. 244, no. 1, pp. 50–56, 1998.
- H. Ohbayashi, K. Yamaki, R. Suzuki, and K. Takagi, “Effects of uroguanylin and guanylin against antigen-induced bronchoconstriction and airway microvascular leakage in sensitized guinea- pigs,” Life Sciences, vol. 62, no. 20, pp. 1833–1844, 1998.
- H. Ohbayashi and K. I. Yamaki, “Both inhalant and intravenous uroguanylin inhibit leukotriene C4-induced airway changes,” Peptides, vol. 21, no. 10, pp. 1467–1472, 2000.
- A. Spreca, S. Simonetti, and M. G. Rambotti, “Atrial natriuretic peptide and guanylin-activated guanylate cyclase isoforms in human sweat glands,” Histochemical Journal, vol. 32, no. 12, pp. 725–731, 2000.
- M. Reinecke, I. David, D. Loffing-Cueni et al., “Localization, expression, and characterization of guanylin in the rat adrenal medulla,” Histochemistry and Cell Biology, vol. 106, no. 4, pp. 367–374, 1996.
- M. Jaleel, R. M. London, S. L. Eber, L. R. Forte, and S. S. Visweswariah, “Expression of the receptor guanylyl cyclase C and its ligands in reproductive tissues of the rat: a potential role for a novel signaling pathway in the epididymis,” Biology of Reproduction, vol. 67, no. 6, pp. 1975–1980, 2002.
- C. M. Sousa, A. Havt, C. F. Santos et al., “The relaxation induced by uroguanylin and the expression of natriuretic peptide receptors in human corpora cavernosa,” Journal of Sexual Medicine, vol. 7, no. 11, pp. 3610–3619, 2010.
- M. A. Valentino, J. E. Lin, A. E. Snook et al., “A uroguanylin-GUCY2C endocrine axis regulates feeding in mice,” The Journal of Clinical Investigation, vol. 121, pp. 3578–3588, 2011.
- K. A. Steinbrecher, T. M. F. Tuohy, K. H. Goss et al., “Expression of guanylin is downregulated in mouse and human intestinal adenomas,” Biochemical and Biophysical Research Communications, vol. 273, no. 1, pp. 225–230, 2000.
- M. B. Cohen, J. A. Hawkins, and D. P. Witte, “Guanylin mRNA expression in human intestine and colorectal adenocarcinoma,” Laboratory Investigation, vol. 78, no. 1, pp. 101–108, 1998.
- K. Shailubhai, H. H. Yu, K. Karunanandaa et al., “Uroguanylin treatment suppresses polyp formation in the Apc(Min/+) mouse and induces apoptosis in human colon adenocarcinoma cells via cyclic GMP,” Cancer Research, vol. 60, no. 18, pp. 5151–5157, 2000.
- G. M. Pitari, M. D. Di Guglielmo, J. Park, S. Schulz, and S. A. Waldman, “Guanylyl cyclase C agonists regulate progression through the cell cycle of human colon carcinoma cells,” Proceedings of the National Academy of Sciences of the United States of America, vol. 98, no. 14, pp. 7846–7851, 2001.
- Z. Li, J. W. Knowles, D. Goyeau et al., “Low salt intake down-regulates the guanylin signaling pathway in rat distal colon,” Gastroenterology, vol. 111, no. 6, pp. 1714–1721, 1996.
- L. Liu, H. Li, T. Underwood et al., “Cyclic GMP-dependent protein kinase activation and induction by exisulind and CP461 in colon tumor cells,” Journal of Pharmacology and Experimental Therapeutics, vol. 299, no. 2, pp. 583–592, 2001.
- M. Suhasini, H. Li, S. M. Lohmann, G. R. Boss, and R. B. Pilz, “Cyclic-GMP-dependent protein kinase inhibits the Ras/mitogen-activated protein kinase pathway,” Molecular and Cellular Biology, vol. 18, no. 12, pp. 6983–6994, 1998.
- K. A. Steinbrecher, S. A. Wowk, J. A. Rudolph, D. P. Witte, and M. B. Cohen, “Targeted inactivation of the mouse guanylin gene results in altered dynamics of colonic epithelial proliferation,” American Journal of Pathology, vol. 161, no. 6, pp. 2169–2178, 2002.
- M. Camici, “Guanylin peptides and colorectal cancer (CRC),” Biomedicine and Pharmacotherapy, vol. 62, no. 2, pp. 70–76, 2008.
- P. Li, J. E. Lin, S. Schulz, G. M. Pitari, and S. A. Waldman, “Can colorectal cancer be prevented or treated by oral hormone replacement therapy?” Current Molecular Pharmacology, vol. 2, no. 3, pp. 285–292, 2009.
- H. R. Wolfe, M. Mendizabal, E. Lleong et al., “In vivo imaging of human colon cancer xenografts in immunodeficient mice using a guanylyl cyclase C-specific ligand,” Journal of Nuclear Medicine, vol. 43, no. 3, pp. 392–399, 2002.
- J. Park, S. Schulz, J. Haaf, J. C. Kairys, and S. A. Waldman, “Ectopic expression of guanylyl cyclase C in adenocarcinomas of the esophagus and stomach,” Cancer Epidemiology Biomarkers and Prevention, vol. 11, no. 8, pp. 739–744, 2002.
- B. Cagir, A. Gelmann, J. Park et al., “Guanylyl cyclase C messenger RNA is a biomarker for recurrent stage II colorectal cancer,” Annals of Internal Medicine, vol. 131, no. 11, pp. 805–812, 1999.
- S. A. Waldman, B. Cagir, J. Rakinic et al., “Use of guanylyl cyclase C for detecting micrometastases in lymph nodes of patients with colon cancer,” Diseases of the Colon and Rectum, vol. 41, no. 3, pp. 310–315, 1998.
- H. Romi, I. Cohen, D. Landau, et al., “Meconium ileus caused by mutations in GUCY2C, encoding the CFTR-activating guanylate cyclase 2C,” The American Journal of Human Genetics, vol. 90, no. 5, pp. 893–899, 2012.
- H. Fukae, H. Kinoshita, S. Fujimoto, M. Nakazato, and T. Eto, “Plasma concentration of uroguanylin in patients on maintenance dialysis therapy,” Nephron, vol. 84, no. 3, pp. 206–210, 2000.
- M. Kikuchi, S. Fujimoto, H. Fukae et al., “Role of uroguanylin, a peptide with natriuretic activity, in rats with experimental nephrotic syndrome,” Journal of the American Society of Nephrology, vol. 16, no. 2, pp. 392–397, 2005.
- A. Baba, S. Fujimoto, M. Kikuchi, T. Kita, and K. Kitamura, “Effects of uroguanylin on natriuresis in experimental nephrotic rats,” Nephrology, vol. 14, no. 1, pp. 80–85, 2009.