Journal of Immunology Research

Journal of Immunology Research / 2018 / Article

Review Article | Open Access

Volume 2018 |Article ID 2645465 |

Bonggi Lee, Kyoung Mi Moon, Choon Young Kim, "Tight Junction in the Intestinal Epithelium: Its Association with Diseases and Regulation by Phytochemicals", Journal of Immunology Research, vol. 2018, Article ID 2645465, 11 pages, 2018.

Tight Junction in the Intestinal Epithelium: Its Association with Diseases and Regulation by Phytochemicals

Academic Editor: Nejat K. Egilmez
Received16 Jul 2018
Revised28 Sep 2018
Accepted14 Oct 2018
Published16 Dec 2018


The intestine plays an essential role in integrating immunity and nutrient digestion and absorption. Adjacent intestinal epithelia form tight junctions (TJs) that are essential to the function of the physical intestinal barrier, regulating the paracellular movement of various substances including ions, solutes, and water across the intestinal epithelium. Studies have shown that TJ dysfunction is highly associated with metabolic and inflammatory diseases. Thus, molecular and nutritional factors that improve TJ activity have gained attention in the pharmaceutical and medicinal fields. This review focuses on the association between TJ and diverse pathological conditions, as well as various molecular and nutritional interventions designed to boost TJ integrity.

1. Introduction

The intestinal epithelium forms the lining of the small intestine. Each epithelium has a brush border, villi, crypt, and basolateral plasma membrane structure. The small intestine not only absorbs nutrients from the diet but also offers a physical barrier—assisted by the tight junctions (TJs) formed by neighboring epithelial cells—and a biological barrier, both of which act against extracellular substances such as microorganisms, antigens, and xenobiotics (Figure 1). Moreover, the small intestine secretes a wide range of hormones that regulate its internal functions as well as energy metabolism throughout the body.

The main function of the small intestine is the absorption of nutrients. The intestinal epithelium expresses digestive enzymes, transporters of specific nutrients, and metabolic enzymes. The small intestine also mediates signal transduction and produces bioactive compounds. The intestinal epithelium responds to various inflammatory and oxidative stresses induced by bacterial toxins, proinflammatory cytokines (TNF-α and IL-1β), and other components through various receptors, including toll-like receptors (TLRs) on the plasma membrane of the epithelium.

TJs contribute to the function of the physical intestinal barrier by regulating the paracellular movement of ions, solutes, and water across the intestinal epithelium, while the detoxification system contributes a biological barrier against xenobiotics. In addition, TJ integrity is related to the functions of the intestinal epithelium. Data from clinical trials and basic science suggest that the TJ barrier plays an essential role in the pathogenesis of systemic and intestinal disorders. Therefore, this review will discuss the association between TJ and various metabolic and inflammatory diseases, as well as the molecular and nutritional controls of intestinal TJ.

2. Tight Junction and Tight Junction-Associated Proteins

TJ is generated by the assembly of multiple proteins located near the apical part of the epithelium between neighboring cells (Figure 2) and controls the permeability of the paracellular transport pathway. TJ plays a pivotal role in maintaining intestinal barrier function and consists of two functional protein categories, integral transmembrane proteins that form a network between adjacent cell membranes and peripheral membrane or plaque proteins. TJ integrity is dynamically regulated by the arrangement of actin and the interaction between integral transmembrane and peripheral membrane proteins. Four integral transmembrane proteins are occludin, claudins, junctional adhesion molecule (JAM), and tricellulin. Peripheral membrane adaptor proteins zonula occludens-1 (ZO-1), ZO-2, and ZO-3 act as bridges to connect integral membrane proteins to the actin cytoskeleton and to other signaling proteins. The phosphorylation, distribution, and expression levels of TJ proteins play a critical role in regulating TJ barrier function. They are tightly regulated by the following intracellular signal transduction pathways: protein kinase C (PKC), A (PKA), and G (PKG) signalings; phosphatase, Rho, myosin light chain (MLC) kinase (MLCK), and MAPK signaling; and the PI3K/Akt pathway [1, 2].

2.1. Occludin

Occludin is highly expressed at cell-cell contact sites and is thought to be important in the assembly and maintenance of TJ. It consists of four transmembrane domains and two extracellular loops. The phosphorylation of occludin correlates with the regulation of its localization and function. Occludin that is phosphorylated at its serine/threonine residues is localized mainly in the membrane, whereas less phosphorylated occludin is found in the cytoplasm. In addition, phosphorylation of occludin appears to control its interaction with other TJ proteins such as ZO-1 [3]. The interaction between occludin and ZO-1 is essential for TJ integrity [4]. Therefore, phosphorylated occludin regulates TJ stability and permeability [5]. In keeping with these observations, occludin knockout mice showed normal TJ structure but exhibited elevated inflammation, hyperplasia, and growth retardation [6]. On the other hand, an enhanced level of occludin plays a role in further improving TJ barrier function and preventing damage to the TJ [7].

2.2. Claudin

Although there is no sequence homology between occludin and claudins, the claudin family also consists of four transmembrane domains and two extracellular loops that construct TJ strands (Figure 1). The claudin family is composed of 23 integral membrane proteins. The extracellular loops of claudin take part in heterophilic and hemophilic interactions with adjacent cells, which generate barriers against or pores for the passage of selective molecules in the paracellular pathways [8, 9]. It is thought that 27 mammalian claudin genes may exist, although their classification as claudins is disputed [10]. When the expression of claudins-1–24 was tested in rat and mouse intestines, all claudins except 6, 16, 19, 22, and 24 were detected by PCR analysis [11]. Although more studies are necessary to determine the exact functions of claudins in TJs, animal studies have indicated the importance of claudins in the integrity of TJs. Claudin-1-deficient mice exhibited abnormal TJ barrier formation, which induced cancer development and metastasis [12]. Mice with claudin-2 or claudin-15 deficiencies in the small intestine reveal that these transmembrane proteins play essential roles in the transepithelial paracellular channel-like permselectivity for extracellular monovalent cations, especially Na(+), in both infants and adults [13].

2.3. Zonula Occludens

The ZO proteins, which include ZO-1, ZO-2, and ZO-3, were the first TJ-specific proteins to be discovered [14]. ZO connects junctional proteins such as occludin and claudin to the actin cytoskeleton, and these protein interactions maintain TJ formation and function. To date, the roles of ZO proteins in TJs are not fully understood. Studies indicate that although ZO-1-deficient cells can maintain the structure of TJs and exhibit normal permeability, the activity of other TJ proteins such as occludin and claudins in assembling TJs was delayed in these cells [8, 15, 16]. On the other hand, the deficiency of ZO-2 or ZO-3 did not affect the formation of TJ in epithelial cell types [15], suggesting that ZO-1 proteins play a more important role in the control of TJ assembly compared to ZO-2 or ZO-3.

3. Disruption of Tight Junction

The integrity of the intestinal epithelial barrier maintained by TJ is crucial to protect the body against stress stimuli related to inflammation and infection. The alteration of TJ homeostasis is thought to induce the pathogenesis of several diseases and vice versa. Factors related to the alteration of TJ homeostasis include proinflammatory cytokines, pathogenic bacteria, lipopolysaccharides (LPS), and pathological conditions.

3.1. Proinflammatory Cytokines

Proinflammatory cytokines such as TNF-α, IL-1β, and IFNγ promote TJ permeability. TNF-α suppresses TJ barrier function due to the activation of the NF-κB pathway and decreased ZO-1 protein level [17]. Conversely, blocking the NF-κB pathway abolishes the TNF-α-mediated opening of the TJ barrier and ZO-1 downregulation. Interestingly, it appears that the TNF-α treatment site in filter-grown Caco-2 cell monolayers was important. TNF-α treatment in the basolateral compartment but not in the apical compartment significantly affected TJ integrity. The detailed molecular mechanism of the action of TNF-α was further studied in vitro. It has been proposed that an increase in MLCK expression and activity is associated with the NF-κB-mediated disruption of TJ [18]. As the MLCK promoter region contains an NF-κB binding site, TNF-α treatment increased MLCK promoter activity and transcription by NF-κB activation [19]. Subsequently, enhanced levels of MLCK protein and its activity promoted TJ permeability in Caco-2 cells. Similarly, IL-1β increased TJ permeability via activation of the NF-κB pathway [20]. MLCK activation by the extracellular signal-regulated kinases 1/2 (ERK1/2) signaling pathways was also related to IL-1β mediated changes in TJ [21, 22]. Unlike TNF-α, IL-1β treatment did not affect the ZO-1 protein level but did suppress the occludin protein level [20].

3.2. Pathogenic Bacteria and Lipopolysaccharides

The roles of pathogenic bacteria and bacterial toxins in the endothelial barrier have been reviewed elsewhere [23, 24]. Enteric pathogenic bacteria such as Escherichia coli (E. coli) and Salmonella typhimurium (S. typhimurium) alter the intestinal epithelial TJ barrier, leading to intestinal inflammation [24]. LPS, a component of the outer walls of gram-negative bacteria, is reported to alter TJ protein assembly, contributing to a leaky small intestine. Indeed, LPS is recognized by TLR4. TLR4 activation by LPS modulates the inflammatory response, which further exacerbates the alteration of TJ. E. coli O111: B4 LPS injection in mice disrupts intestinal epithelial TJ function in the ileal and colonic epithelia [25]. LPS also induces systemic inflammation, leading to altered expression and localization of TJ proteins such as ZO-1 and occludin. Apical LPS treatment increases TJ permeability and induces epithelial apoptosis by activating caspase-3 in duodenal epithelial monolayers [26]. Thus, it is thought that pathogenic bacteria and LPS disrupt intestinal TJ integrity by elevating various inflammatory signaling pathways, resulting in a leaky intestine.

3.3. Pathological Conditions

Certain pathological conditions are correlated with a defective intestinal TJ barrier, including inflammatory bowel disease (IBD), obesity, nonalcoholic steatohepatitis (NASH), and nonalcoholic fatty liver disease (NAFLD) (Table 1) [27].

DiseasesReported intestinal symptomReferences

Inflammatory bowel diseaseDysfunction of the intestinal barrier, chronic inflammation
Crohn’s diseaseAn abnormal intestinal structure, a leaky small intestine, a high level of intestinal inflammation[34]
ObesityThe impairment of intestinal barrier function, alteration in microbiome population[37]
NAFLDAbnormal morphologies of crypts and villi in duodenal mucosa[43]
Coeliac disease (autoimmune enteropathy)Dysfunction of the intestinal barrier (increased gliadin permeation and related immune response)
Type 1 diabetes mellitusGut microbiota dysbiosis, increased intestinal permeability, heightened immune activation

3.3.1. IBD

IBD involves a wide range of chronic remitting diseases of which ulcerative colitis (UC) and Crohn’s disease (CD) are likely the most abundant [28]. IBD, usually known to involve a high level of intestinal inflammation, is associated with dysregulation of TJ [29]. IBD affects many components of the epithelial barrier including abnormal changes in the epithelium itself, its adhesion molecules, and the altered production of mucus and antimicrobial peptides. Together, these alterations result in the loss of solutes and fluid across the epithelial barrier, contributing to leak-flux diarrhea and elevated antigen translocation [28]. Antigen translocation in the lamina propria causes inflammation derived from circulating and resident immune cells, leading to further disruption of the barrier function [28, 30]. CD and UC are closely related to epithelial apoptosis [31], which is also a significant contributor to barrier leakiness. The apoptotic enterocytes invade the lumen while the remaining enterocytes redistribute the junctional proteins along the lateral cell membranes, leading to contraction of the surrounding epithelium and maintenance of barrier integrity [28, 32]. However, active UC is associated with the redistribution and decreased expression of claudin-1, claudin-4, claudin-7, and occludin, as well as a notable increase in claudin-2 expression [27, 33]. CD is also associated with both the redistribution and decreased expression of claudin-3, claudin-5, and claudin-8, as well as increased expression of claudin-2 [27, 33]. Furthermore, CD is known to present an abnormal intestinal structure with a high level of intestinal inflammation [34]. For example, patients with CD have elevated levels of plasma, fecal, and intestinal TNF-αs, which also can accelerate TJ dysfunction [35]. Altogether, the redistribution and alteration of TJ proteins, as well as inflammatory responses, are closely associated with barrier dysfunction in patients with UC or CD.

3.3.2. Obesity

Obesity is associated with increased intestinal permeability. The impairment of intestinal barrier function due to the altered assembly of TJ proteins was observed in genetically obese mouse models including ob/ob and db/db mice [36]. The ob/ob and db/db mice exhibited an increase in intestinal permeability and significantly higher plasma endotoxin and proinflammatory cytokines such as IL-1β, IL-6, INFγ, and TNF-α compared to wild-type mice. TJ alteration has also been found in animal models with high-fat diet-induced obesity (DIO) and diabetes [37, 38]. High-fat diet caused suppression of the levels of occludin, claudin-1, claudin-3, and JAM-1, along with an increased level of plasma TNF-α in the small intestinal mucosa of rats [38]. DIO changed the gut bacterial population and TJ integrity in mice [37]. This study suggested that the microbiome is associated with DIO-induced endotoxemia and metabolic syndrome. These effects are possibly mediated by increased gut permeability followed by elevated LPS absorption. In support of this, antibiotics decreased circulating LPS levels, gut permeability, and metabolic syndrome [37]. Another study showed that the altered gut microbiota population in DIO mice is related to inflammation and gut permeability, partly due to the reduced expression of TJ-related genes including ZO-1 and occludin [39]. Involvement of LPS and TLR4 in DIO-induced TJ permeability has also been reported [40]. In the obese animals, MLC phosphorylation was significantly increased, causing disruption of TJ [40]. Antibiotics or prebiotics prevented the alteration of gut barrier function found in obesity and diabetes [37, 39]. These data indicate that obesity-induced inflammation is associated with changes in TJ integrity and gut microbiota.

3.3.3. NASH and NAFLD

NASH and NAFLD, obesity-related fatty liver diseases, are also known to be associated with TJ dysfunction. The molecular mechanisms of these chronic liver diseases are not clear, but the interaction of microbiota, gut-liver axis, and obesity is emerging as a mechanism of the development of obesity-related liver disease [41]. Changes in the composition of gut microbiota in NAFLD increased circulating plasma LPS, subsequently triggering inflammation. These plasma LPS and proinflammatory cytokines concurrently increase intestinal permeability [42]. In patients with NAFLD, higher levels of insulin, blood pressure, serum triglycerides, total cholesterol, and liver enzymes were observed [43]. Patients with NAFLD also exhibited abnormal crypt and villi morphologies in duodenal mucosa, increased TJ permeability, and overgrowth of small intestinal bacteria. Increased intestinal permeability may cause the pathogenesis of hepatic fat deposition. In NAFLD, this increase in permeability mainly results from ZO-1 translocation in the crypt. Overall, inflammatory diseases such as inflammatory bowel disease, obesity, NASH, and NAFLD are highly associated with the disruption of TJ integrity.

4. Dietary Intervention to Maintain TJ Integrity

In order to develop a dietary intervention for TJ integrity, many factors in addition to efficacy should be considered, including safety, stability during processing and shelf life, the cost of developing raw ingredients, and sensory quality [44]. Regulation is also a factor to be considered, though food components are generally recognized as safe (GRAS). Given these criteria, bioactive food components are good candidate agents. Here, we focus on dietary food components to maintain TJ integrity.

4.1. Role of Phytochemicals in Tight Junction Integrity

The beneficial role of dietary phytochemicals in TJ integrity has been reviewed previously [45, 46]. Of the many groups of phytochemicals, the effects of flavonoids (C6C3C6) on intestinal permeability have been widely studied. These secondary metabolites are widespread throughout the plant kingdom. Since the absorption rate of these phytochemicals is generally limited [45], it is likely that they reach both small and large intestines, affecting intestinal permeability. The effects of some of the most extensively studied flavonoids on the suppression of the paracellular permeability of epithelial cells that form TJs in the small intestine are summarized in Table 2. Next, we discuss the following phytochemicals: quercetin, berberine, genistein, kaempferol, and curcumin (Figure 3).

TreatmentConc.SystemStimuliTight junction protein affectedPotential targeting pathwaysRef.

Quercetin200 μMCaco-2None↑ claudin-4↓ protein kinase A (PKA) or PKG[50]
100 μMCaco-2None↑ ZO-2, occludin, claudin-1 and -4↓ PKCδ[51]

Berberine100 μMCaco-2NoneNot studiedNot studied[55]
100 μMCaco-2TNF-α, IFNγ↑ occludinNot studied[56]
200 mg/kgMouseLPS↑ occludin, ZO-1, claudin-1 and -4↓ myosin light chain kinase, ↓ nuclear factor-κB (NF-κB)[53]
375 mg/kg/dayRatStreptozotocin↑ occludin, ZO-1, claudin-1↓ TLR4/MyD88/NF-κB signaling pathways[54]

Genistein300 μMCaco-2NoneNot studiedLocalization of filamentous actin in the perijunctional area[59]

Kaempferol100 μMCaco-2None↑ occludin, claudin-1 and -3, and ZO-1; ↑ ZO-2 and claudin-4; phosphorylation of occludinNot studied[63]

CurcuminμMCaco-2TNF-α↑ ZO-1↓ NF-κB[17]
μMCaco-2TNF-αNot studied↓ myosin light chain kinase, ↓ NF-κB[19]
μMCaco-2IL-1βNot studied↓ NF-κB[20]
30 μMCaco-2 BBeLeptin↑ ZO-3, claudin-5, occludin↓ leptin signaling pathway[67]

4.1.1. Quercetin

Quercetin is one of the most widely distributed flavonoids in plants such as fruits, vegetables, and grains. Of its many biological activities, it is well-known for protecting cells from oxidative and inflammation-associated injuries. The biological functions of quercetin are closely associated with the regulation of key enzymes including PI-3 kinase, NF-κB, PKC, tyrosine kinase, and the MAPK family [45, 4749]; these enzymes (especially PKC and MAPKs) and their downstream signaling pathways are closely related to the assembly and integrity of TJ functions [45]. Thus, various studies have been undertaken to elucidate the roles of quercetin in TJ integrity. Quercetin augmented TJ barrier function in Caco-2 cells in the absence of any stimuli such as proinflammatory cytokines [50]. Treatment with 200 μM quercetin for 24 hours specifically increased the expression of claudin-4 but not other TJ proteins such as occludin and claudin-1, -3, and -7. Another study showed that quercetin treatment elevated the transepithelial electrical resistance (TER) across the monolayers and reduced lucifer yellow flux, a paracellular marker [51]. In order to identify the cellular mechanisms involved in the beneficial effect of quercetin on TJ, several protein kinase inhibitors were used. Staurosporine, a general protein kinase inhibitor, and H7, an inhibitor of PKA and PKG, abrogated the preventive function of quercetin on TJ, indicating that the potential inhibition of PKA and PKG contributes to the protective effect on TJ by quercetin. Another study reported that 100 μM quercetin reinforces TJ integrity through the modulation of multiple TJ-related proteins including claudin-1 and -4, ZO-2, and occludin by suppressing PKCδ [51]. Thus, it appears that the suppression of multiple protein kinases contributes to quercetin-mediated TJ integrity.

4.1.2. Berberine

Berberine, found in Coptidis rhizome, is an isoquinoline alkaloid that has been used as a traditional Chinese medicine for thousands of years to treat gastrointestinal diseases, diarrhea, and bacterial infections [52], all of which are associated with the disruption of intestinal barrier function and TJ integrity. Consequently, the roles of berberine in intestinal TJ integrity have been studied both in vivo and in vitro. When the protective effect of berberine on intestinal damage was investigated in a mouse model of endotoxinemia, intragastric pretreatment with berberine partially prevented the ultrastructural damage of TJ partly by reversing the LPS-mediated redistribution of TJ proteins including occludin, ZO-1, claudin-1, or claudin-4 in colon epithelium and in membrane microdomains [53]. The protective effect of berberine on intestinal mucosal barrier dysfunction was also reported in type 2 diabetic rats [54]. Pretreatment with berberine for nine weeks significantly ameliorated the disruption of intestinal permeability, proinflammatory intestinal changes, and abnormal changes in gut-derived hormones [54]. In vitro studies also examined the beneficial effects of berberine on TJ integrity. Berberine at 100 μM enhanced TJ in Caco-2 cells without any stimulation [55]. The combined treatment of Caco-2 cells with TNF-α and IFNγ induced TJ dysfunction through the cytosolic distribution of occludin; treatment with berberine prevented this dysfunction [56]. Although the mechanism underlying the berberine-mediated protection of TJ integrity requires further elucidation, studies indicate that the inhibition of the NF-κB signaling pathway is involved in the beneficial effect of berberine on TJ. The NF-κB signaling pathway is central in stimulating the transcription of diverse inflammatory genes. It has been reported that the intestinal NF-κB p65 subunit is activated in the endotoxinemic state, but berberine treatment reduced these effects [53]. In addition, berberine supplementation suppressed the NF-κB signaling pathway in the intestine of diabetic rats [54]. The berberine-mediated inhibition of NF-κB signaling is partially due to the suppression of inhibitory factor κB (I-κB) kinase, which stabilizes I-κB, thereby inhibiting nuclear translocation of the NF-κB p65 subunit [53].

4.1.3. Genistein

Genistein is a major isoflavone present in soybeans. Since it is well-known as a potent inhibitor of protein tyrosine kinases, many studies have focused on the effects of genistein on signal transduction [45]. As mentioned earlier, the phosphorylation status of TJ proteins is highly associated with TJ function and structure [57, 58]. Thus, various studies have reported the roles of genistein in TJ integrity. Genistein tightened TJ in Caco-2 cells [59]. When enteric bacteria such as E. coli and S. typhimurium interacted with intestinal cells, TJ barriers were opened, but genistein at 300 μM prevented this opening and blocked the invasion of enteric bacteria. Another study showed that genistein improved intestinal TJ barrier dysfunction induced by oxidative stress [60]. Treatment with a mixture of xanthine oxidase and xanthine, which induces oxidative stress, reduced the TER and elevated [3H]-mannitol flux, both of which represent TJ permeability; the coadministration of genistein at 300 μM inhibited these changes partially by suppressing oxidative stress-induced c-Src kinase, followed by the inhibition of the tyrosine phosphorylation of TJ proteins [60]. The protective effects of genistein on TJ permeability are partly ascribed to the inhibitory effect on the phosphorylation of TJ proteins. Occludin undergoes tyrosine phosphorylation when TJ function is impaired by various factors [61], but genistein appears to suppress this process [45]. Genistein also ameliorates oxidative stress-induced TJ barrier dysfunction. Oxidative stress induced by the mixture of xanthine oxidase and xanthine, which produces superoxide anions in culture media, reduced TER and elevated [3H]-mannitol flux, markers of TJ permeability in Caco-2 cells; these alterations were reversed by the coadministration of genistein [60]. As an underlying mechanism, genistein appears to inhibit oxidative stress-stimulated c-Src kinase activation, preventing the tyrosine phosphorylation of TJ proteins (ZO-1 and occludin) and adherence junction (AJ) proteins (E-cadherin). These actions suppress the disassembly of TJ and AJ proteins from the junctional complex [45, 60].

4.1.4. Kaempferol

Kaempferol is a flavonol found in fruits and vegetables including apples, grapes, broccoli, kale, and chives. Numerous in vivo and in vitro studies have demonstrated that kaempferol and kaempferol glycosides exhibit health-promoting effects including antioxidant and anti-inflammatory benefits, which are associated with the maintenance of TJ integrity [62]. When the roles of kaempferol in TJ functions were investigated, it was found to strengthen the TJ barrier in Caco-2 cells [63]. Kaempferol notably elevated TER across the monolayers. The administration of kaempferol at 100 μM promoted the protein expression of TJ-related proteins ZO-1 and -2, occludin, and claudin-1, -3, and -4 and elevated the phosphorylation of occludin. Consistently, microscopic analysis indicated that kaempferol stimulated the assembly of occludin and claudin-3 at TJs [63]. As an underlying mechanism, the membrane lipid microdomain is associated with the kaempferol-mediated beneficial effects on TJ as evidenced by the inhibition of kaempferol-induced elevation of TER after extraction of cholesterol with methyl-β-cyclodextrin and kaempferol-mediated increase in the TJ protein distributions in the cholesterol-rich lipid microdomain [63]. These data suggest that the membrane lipid microdomain is closely related to the increase in TJ protein assembly and intestinal TJ integrity by kaempferol [63].

4.1.5. Curcumin

Curcumin is a biologically active polyphenolic compound found in the dietary spice turmeric. It has long been used in Asian countries as a remedy for various diseases including diabetes, liver diseases, infectious diseases, and cancers [64]. It has been shown to suppress chronic inflammatory diseases despite poor bioavailability [65]. Thus, it has been hypothesized that curcumin may act on intestinal epithelial cells to regulate systemic inflammation [66]. Consequently, a potential role for curcumin in protecting TJ integrity has been proposed. When Caco-2 cells were stimulated by the proinflammatory cytokines TNF-α or IL-1β, epithelial TJ permeability was significantly increased through the activation of the NF-κB pathway. Curcumin pretreatment abolished proinflammatory cytokine-deteriorated TJ barrier function. Moreover, curcumin treatment prevents apical leptin-impaired TJ by suppressing the leptin signaling pathway in Caco-2 BBe monolayers [67]. Curcumin suppressed the gene expression of leptin-induced proinflammatory cytokines such as IL-6 and TNF-α and leptin-induced genes such as c-fos and c-jun. Moreover, curcumin blocked leptin-altered TJ gene expression including ZO-1, claudin-5, and occludin. Another study using intestinal epithelial cells showed that pretreatment with curcumin ameliorated the LPS-mediated disruption of intestinal barrier function [66]. Although the underlying mechanisms must be further investigated, various studies used curcumin as an inhibitor of the NF-κB pathway in proinflammatory cytokine-induced TJ alteration [17, 19, 20]. It suppresses NF-κB activity by inhibiting I-κB kinase followed by the stabilization of I-κB [68, 69]. Another mechanism underlying the curcumin-mediated protective effect on TJ includes the inhibition of the IL-1β/p38 signaling cascade. IL-1β-mediated activation of p38 MAP kinase results in the activation of MLCK. MLCK-mediated phosphorylation of myosin light chain impairs TJ structure and elevates intestinal permeability [66].

5. Conclusions

TJ is associated with physical intestinal barrier function, regulating the paracellular movement of various substances across the intestinal epithelium. Studies reveal that TJ dysfunction is closely related to inflammatory and metabolic disorders including IBD, NASH, NAFLD, and obesity via the disruption of TJ barrier functions. Thus, the maintenance of TJ integrity is likely a good strategy to prevent and/or treat these diseases. Although natural compounds such as quercetin, berberine, genistein, kaempferol, and curcumin have been reported to improve TJ integrity by controlling TJ-related proteins and inflammatory signaling pathways (Figure 3), more detailed molecular studies on the effects of natural compounds on intestinal TJ functions are necessary to develop preventive medicine and pharmaceutical agents against inflammatory and metabolic diseases.

Conflicts of Interest

The authors declare that there is no conflict of interest regarding the publication of this paper.

Authors’ Contributions

Lee, B. and Moon, K. M. wrote the manuscript. Kim, C. Y. designed and wrote the manuscript.


This work was supported by the 2015 Yeungnam University Research Grant.


  1. L. Gonzalez-Mariscal, R. Tapia, and D. Chamorro, “Crosstalk of tight junction components with signaling pathways,” Biochimica et Biophysica Acta (BBA) - Biomembranes, vol. 1778, no. 3, pp. 729–756, 2008. View at: Publisher Site | Google Scholar
  2. N. S. Harhaj and D. A. Antonetti, “Regulation of tight junctions and loss of barrier function in pathophysiology,” The International Journal of Biochemistry & Cell Biology, vol. 36, no. 7, pp. 1206–1237, 2004. View at: Publisher Site | Google Scholar
  3. R. Rao, “Occludin phosphorylation in regulation of epithelial tight junctions,” Annals of the New York Academy of Sciences, vol. 1165, no. 1, pp. 62–68, 2009. View at: Publisher Site | Google Scholar
  4. G. Bazzoni and E. Dejana, “Endothelial cell-to-cell junctions: molecular organization and role in vascular homeostasis,” Physiological Reviews, vol. 84, no. 3, pp. 869–901, 2004. View at: Publisher Site | Google Scholar
  5. T. Murakami, E. A. Felinski, and D. A. Antonetti, “Occludin phosphorylation and ubiquitination regulate tight junction trafficking and vascular endothelial growth factor-induced permeability,” The Journal of Biological Chemistry, vol. 284, no. 31, pp. 21036–21046, 2009. View at: Publisher Site | Google Scholar
  6. M. Saitou, M. Furuse, H. Sasaki et al., “Complex phenotype of mice lacking occludin, a component of tight junction strands,” Molecular Biology of the Cell, vol. 11, no. 12, pp. 4131–4142, 2000. View at: Publisher Site | Google Scholar
  7. K. M. McCarthy, I. B. Skare, M. C. Stankewich et al., “Occludin is a functional component of the tight junction,” Journal of Cell Science, vol. 109, 9, pp. 2287–2298, 1996. View at: Google Scholar
  8. S. H. Lee, “Intestinal permeability regulation by tight junction: implication on inflammatory bowel diseases,” Intestinal Research, vol. 13, no. 1, pp. 11–18, 2015. View at: Publisher Site | Google Scholar
  9. C. M. van Itallie and J. M. Anderson, “Claudins and epithelial paracellular transport,” Annual Review of Physiology, vol. 68, no. 1, pp. 403–429, 2006. View at: Publisher Site | Google Scholar
  10. G. J. Maher, E. N. Hilton, J. E. Urquhart et al., “The cataract-associated protein TMEM114, and TMEM235, are glycosylated transmembrane proteins that are distinct from claudin family members,” FEBS Letters, vol. 585, no. 14, pp. 2187–2192, 2011. View at: Publisher Site | Google Scholar
  11. D. Günzel and A. S. L. Yu, “Claudins and the modulation of tight junction permeability,” Physiological Reviews, vol. 93, no. 2, pp. 525–569, 2013. View at: Publisher Site | Google Scholar
  12. M. Furuse, M. Hata, K. Furuse et al., “Claudin-based tight junctions are crucial for the mammalian epidermal barrier: a lesson from claudin-1-deficient mice,” The Journal of Cell Biology, vol. 156, no. 6, pp. 1099–1111, 2002. View at: Publisher Site | Google Scholar
  13. A. Tamura, H. Hayashi, M. Imasato et al., “Loss of claudin-15, but not claudin-2, causes Na+ deficiency and glucose malabsorption in mouse small intestine,” Gastroenterology, vol. 140, no. 3, pp. 913–923, 2011. View at: Publisher Site | Google Scholar
  14. J. Haskins, L. Gu, E. S. Wittchen, J. Hibbard, and B. R. Stevenson, “ZO-3, a novel member of the MAGUK protein family found at the tight junction, interacts with ZO-1 and occludin,” The Journal of Cell Biology, vol. 141, no. 1, pp. 199–208, 1998. View at: Publisher Site | Google Scholar
  15. S. Tsukita, T. Katsuno, Y. Yamazaki, K. Umeda, A. Tamura, and S. Tsukita, “Roles of ZO-1 and ZO-2 in establishment of the belt-like adherens and tight junctions with paracellular permselective barrier function,” Annals of the New York Academy of Sciences, vol. 1165, no. 1, pp. 44–52, 2009. View at: Publisher Site | Google Scholar
  16. K. Umeda, T. Matsui, M. Nakayama et al., “Establishment and characterization of cultured epithelial cells lacking expression of ZO-1,” The Journal of Biological Chemistry, vol. 279, no. 43, pp. 44785–44794, 2004. View at: Publisher Site | Google Scholar
  17. T. Y. Ma, G. K. Iwamoto, N. T. Hoa et al., “TNF-α-induced increase in intestinal epithelial tight junction permeability requires NF-κB activation,” American Journal of Physiology Gastrointestinal and Liver Physiology, vol. 286, no. 3, pp. G367–G376, 2004. View at: Publisher Site | Google Scholar
  18. T. Y. Ma, M. A. Boivin, D. Ye, A. Pedram, and H. M. Said, “Mechanism of TNF-α modulation of Caco-2 intestinal epithelial tight junction barrier: role of myosin light-chain kinase protein expression,” American Journal of Physiology Gastrointestinal and Liver Physiology, vol. 288, no. 3, pp. G422–G430, 2005. View at: Publisher Site | Google Scholar
  19. D. Ye, I. Ma, and T. Y. Ma, “Molecular mechanism of tumor necrosis factor-α modulation of intestinal epithelial tight junction barrier,” American Journal of Physiology. Gastrointestinal and Liver Physiology, vol. 290, no. 3, pp. G496–G504, 2006. View at: Publisher Site | Google Scholar
  20. R. M. Al-Sadi and T. Y. Ma, “IL-1β causes an increase in intestinal epithelial tight junction permeability,” The Journal of Immunology, vol. 178, no. 7, pp. 4641–4649, 2007. View at: Publisher Site | Google Scholar
  21. R. Al-Sadi, D. Ye, K. Dokladny, and T. Y. Ma, “Mechanism of IL-1β-induced increase in intestinal epithelial tight junction permeability,” The Journal of Immunology, vol. 180, no. 8, pp. 5653–5661, 2008. View at: Publisher Site | Google Scholar
  22. R. Al-Sadi, D. Ye, H. M. Said, and T. Y. Ma, “Cellular and molecular mechanism of interleukin-1β modulation of CACO-2 intestinal epithelial tight junction barrier,” Journal of Cellular and Molecular Medicine, vol. 15, no. 4, pp. 970–982, 2011. View at: Publisher Site | Google Scholar
  23. E. Lemichez, M. Lecuit, X. Nassif, and S. Bourdoulous, “Breaking the wall: targeting of the endothelium by pathogenic bacteria,” Nature Reviews Microbiology, vol. 8, no. 2, pp. 93–104, 2010. View at: Publisher Site | Google Scholar
  24. J. Berkes, V. K. Viswanathan, S. D. Savkovic, and G. Hecht, “Intestinal epithelial responses to enteric pathogens: effects on the tight junction barrier, ion transport, and inflammation,” Gut, vol. 52, no. 3, pp. 439–451, 2003. View at: Publisher Site | Google Scholar
  25. X. Han, M. P. Fink, R. Yang, and R. L. Delude, “Increased iNOS activity is essential for intestinal epithelial tight junction dysfunction in endotoxemic mice,” Shock, vol. 21, no. 3, pp. 261–270, 2004. View at: Publisher Site | Google Scholar
  26. A. C. Chin, A. N. Flynn, J. P. Fedwick, and A. G. Buret, “The role of caspase-3 in lipopolysaccharide-mediated disruption of intestinal epithelial tight junctions,” Canadian Journal of Physiology and Pharmacology, vol. 84, no. 10, pp. 1043–1050, 2006. View at: Publisher Site | Google Scholar
  27. N. A. Hering, M. Fromm, and J.-D. Schulzke, “Determinants of colonic barrier function in inflammatory bowel disease and potential therapeutics,” The Journal of Physiology, vol. 590, no. 5, pp. 1035–1044, 2012. View at: Publisher Site | Google Scholar
  28. F. E. O. Holmberg, J. Pedersen, P. Jorgensen, C. Soendergaard, K. B. Jensen, and O. H. Nielsen, “Intestinal barrier integrity and inflammatory bowel disease: stem cell-based approaches to regenerate the barrier,” Journal of Tissue Engineering and Regenerative Medicine, vol. 12, no. 4, pp. 923–935, 2018. View at: Publisher Site | Google Scholar
  29. K. L. Edelblum and J. R. Turner, “The tight junction in inflammatory disease: communication breakdown,” Current Opinion in Pharmacology, vol. 9, no. 6, pp. 715–720, 2009. View at: Publisher Site | Google Scholar
  30. M. A. McGuckin, R. Eri, L. A. Simms, T. H. Florin, and G. Radford-Smith, “Intestinal barrier dysfunction in inflammatory bowel diseases,” Inflammatory Bowel Diseases, vol. 15, no. 1, pp. 100–113, 2009. View at: Publisher Site | Google Scholar
  31. J. M. Blander, “Death in the intestinal epithelium—basic biology and implications for inflammatory bowel disease,” The FEBS Journal, vol. 283, no. 14, pp. 2720–2730, 2016. View at: Publisher Site | Google Scholar
  32. A. M. Marchiando, L. Shen, W. V. Graham et al., “The epithelial barrier is maintained by in vivo tight junction expansion during pathologic intestinal epithelial shedding,” Gastroenterology, vol. 140, no. 4, pp. 1208–1218.e2, 2011. View at: Publisher Site | Google Scholar
  33. J. Luettig, R. Rosenthal, C. Barmeyer, and J. D. Schulzke, “Claudin-2 as a mediator of leaky gut barrier during intestinal inflammation,” Tissue Barriers, vol. 3, no. 1-2, article e977176, pp. 1-2, 2015. View at: Publisher Site | Google Scholar
  34. D. Hollander, “Crohn’s disease--a permeability disorder of the tight junction?” Gut, vol. 29, no. 12, pp. 1621–1624, 1988. View at: Publisher Site | Google Scholar
  35. P. R. Gibson, “Increased gut permeability in Crohn’s disease: is TNF the link?” Gut, vol. 53, no. 12, pp. 1724-1725, 2004. View at: Publisher Site | Google Scholar
  36. P. Brun, I. Castagliuolo, V. Di Leo et al., “Increased intestinal permeability in obese mice: new evidence in the pathogenesis of nonalcoholic steatohepatitis,” American Journal of Physiology Gastrointestinal and Liver Physiology, vol. 292, no. 2, pp. G518–G525, 2007. View at: Publisher Site | Google Scholar
  37. P. D. Cani, R. Bibiloni, C. Knauf et al., “Changes in gut microbiota control metabolic endotoxemia-induced inflammation in high-fat diet-induced obesity and diabetes in mice,” Diabetes, vol. 57, no. 6, pp. 1470–1481, 2008. View at: Publisher Site | Google Scholar
  38. T. Suzuki and H. Hara, “Dietary fat and bile juice, but not obesity, are responsible for the increase in small intestinal permeability induced through the suppression of tight junction protein expression in LETO and OLETF rats,” Nutrition & metabolism, vol. 7, no. 1, p. 19, 2010. View at: Publisher Site | Google Scholar
  39. P. D. Cani, S. Possemiers, T. Van de Wiele et al., “Changes in gut microbiota control inflammation in obese mice through a mechanism involving GLP-2-driven improvement of gut permeability,” Gut, vol. 58, no. 8, pp. 1091–1103, 2009. View at: Publisher Site | Google Scholar
  40. C. B. de La Serre, C. L. Ellis, J. Lee, A. L. Hartman, J. C. Rutledge, and H. E. Raybould, “Propensity to high-fat diet-induced obesity in rats is associated with changes in the gut microbiota and gut inflammation,” American Journal of Physiology Gastrointestinal and Liver Physiology, vol. 299, no. 2, pp. G440–G448, 2010. View at: Publisher Site | Google Scholar
  41. P. Vajro, G. Paolella, and A. Fasano, “Microbiota and gut–liver axis: their influences on obesity and obesity-related liver disease,” Journal of Pediatric Gastroenterology and Nutrition, vol. 56, no. 5, pp. 461–468, 2013. View at: Publisher Site | Google Scholar
  42. G. Musso, R. Gambino, and M. Cassader, “Gut microbiota as a regulator of energy homeostasis and ectopic fat deposition: mechanisms and implications for metabolic disorders,” Current Opinion in Lipidology, vol. 21, no. 1, pp. 76–83, 2010. View at: Publisher Site | Google Scholar
  43. L. Miele, V. Valenza, G. La Torre et al., “Increased intestinal permeability and tight junction alterations in nonalcoholic fatty liver disease,” Hepatology, vol. 49, no. 6, article 1877, 1887 pages, 2009. View at: Publisher Site | Google Scholar
  44. E. M. Kovacs and D. J. Mela, “Metabolically active functional food ingredients for weight control,” Obesity Reviews, vol. 7, no. 1, pp. 59–78, 2006. View at: Publisher Site | Google Scholar
  45. T. Suzuki and H. Hara, “Role of flavonoids in intestinal tight junction regulation,” The Journal of Nutritional Biochemistry, vol. 22, no. 5, pp. 401–408, 2010. View at: Publisher Site | Google Scholar
  46. D. Ulluwishewa, R. C. Anderson, W. C. McNabb, P. J. Moughan, J. M. Wells, and N. C. Roy, “Regulation of tight junction permeability by intestinal bacteria and dietary components,” The Journal of Nutrition, vol. 141, no. 5, pp. 769–776, 2011. View at: Publisher Site | Google Scholar
  47. G. Agullo, L. Gamet-Payrastre, S. Manenti et al., “Relationship between flavonoid structure and inhibition of phosphatidylinositol 3-kinase: a comparison with tyrosine kinase and protein kinase C inhibition,” Biochemical Pharmacology, vol. 53, no. 11, pp. 1649–1657, 1997. View at: Publisher Site | Google Scholar
  48. L. Gamet-Payrastre, S. Manenti, M.-P. Gratacap, J. Tulliez, H. Chap, and B. Payrastre, “Flavonoids and the inhibition of PKC and PI 3-kinase,” General Pharmacology: The Vascular System, vol. 32, no. 3, pp. 279–286, 1999. View at: Publisher Site | Google Scholar
  49. Y. Ishikawa, H. Sugiyama, E. Stylianou, and M. Kitamura, “Bioflavonoid quercetin inhibits interleukin-1-induced transcriptional expression of monocyte chemoattractant protein-1 in glomerular cells via suppression of nuclear factor-κB,” Journal of the American Society of Nephrology, vol. 10, no. 11, pp. 2290–2296, 1999. View at: Google Scholar
  50. M. Amasheh, S. Schlichter, S. Amasheh et al., “Quercetin enhances epithelial barrier function and increases claudin-4 expression in Caco-2 cells,” The Journal of Nutrition, vol. 138, no. 6, pp. 1067–1073, 2008. View at: Publisher Site | Google Scholar
  51. T. Suzuki and H. Hara, “Quercetin enhances intestinal barrier function through the assembly of zonnula occludens-2, occludin, and claudin-1 and the expression of claudin-4 in Caco-2 Cells,” The Journal of Nutrition, vol. 139, no. 5, pp. 965–974, 2009. View at: Publisher Site | Google Scholar
  52. M. Zhang, Y. Long, Y. Sun et al., “Evidence for the complementary and synergistic effects of the three-alkaloid combination regimen containing berberine, hypaconitine and skimmianine on the ulcerative colitis rats induced by trinitrobenzene-sulfonic acid,” European Journal of Pharmacology, vol. 651, no. 1–3, pp. 187–196, 2011. View at: Publisher Site | Google Scholar
  53. L. Gu, N. Li, J. Gong, Q. Li, W. Zhu, and J. Li, “Berberine ameliorates intestinal epithelial tight-junction damage and down-regulates myosin light chain kinase pathways in a mouse model of endotoxinemia,” The Journal of Infectious Diseases, vol. 203, no. 11, pp. 1602–1612, 2011. View at: Publisher Site | Google Scholar
  54. J. Gong, M. Hu, Z. Huang et al., “Berberine attenuates intestinal mucosal barrier dysfunction in type 2 diabetic rats,” Frontiers in Pharmacology, vol. 8, p. 42, 2017. View at: Publisher Site | Google Scholar
  55. L. Gu, N. Li, Q. Li et al., “The effect of berberine in vitro on tight junctions in human Caco-2 intestinal epithelial cells,” Fitoterapia, vol. 80, no. 4, pp. 241–248, 2009. View at: Publisher Site | Google Scholar
  56. N. Li, L. Gu, L. Qu et al., “Berberine attenuates pro-inflammatory cytokine-induced tight junction disruption in an in vitro model of intestinal epithelial cells,” European Journal of Pharmaceutical Sciences, vol. 40, no. 1, pp. 1–8, 2010. View at: Publisher Site | Google Scholar
  57. V. Nunbhakdi-Craig, T. Machleidt, E. Ogris, D. Bellotto, C. L. White, and E. Sontag, “Protein phosphatase 2A associates with and regulates atypical PKC and the epithelial tight junction complex,” Journal of Cell Biology, vol. 158, no. 5, pp. 967–978, 2002. View at: Publisher Site | Google Scholar
  58. A. Sakakibara, M. Furuse, M. Saitou, Y. Ando-Akatsuka, and S. Tsukita, “Possible involvement of phosphorylation of occludin in tight junction formation,” The Journal of Cell Biology, vol. 137, no. 6, pp. 1393–1401, 1997. View at: Publisher Site | Google Scholar
  59. C. L. Wells, R. P. Jechorek, K. M. Kinneberg, S. M. Debol, and S. L. Erlandsen, “The isoflavone genistein inhibits internalization of enteric bacteria by cultured Caco-2 and HT-29 enterocytes,” The Journal of Nutrition, vol. 129, no. 3, pp. 634–640, 1999. View at: Publisher Site | Google Scholar
  60. R. K. Rao, S. Basuroy, V. U. Rao, K. J. Karnaky Jr., and A. Gupta, “Tyrosine phosphorylation and dissociation of occludin–ZO-1 and E-cadherin–β-catenin complexes from the cytoskeleton by oxidative stress,” The Biochemical Journal, vol. 368, no. 2, pp. 471–481, 2002. View at: Publisher Site | Google Scholar
  61. G. Kale, A. P. Naren, P. Sheth, and R. K. Rao, “Tyrosine phosphorylation of occludin attenuates its interactions with ZO-1, ZO-2, and ZO-3,” Biochemical and Biophysical Research Communications, vol. 302, no. 2, pp. 324–329, 2003. View at: Publisher Site | Google Scholar
  62. J. M. Calderon-Montano, E. Burgos-Moron, C. Perez-Guerrero, and M. Lopez-Lazaro, “A review on the dietary flavonoid kaempferol,” Mini-Reviews in Medicinal Chemistry, vol. 11, no. 4, pp. 298–344, 2011. View at: Publisher Site | Google Scholar
  63. T. Suzuki, S. Tanabe, and H. Hara, “Kaempferol enhances intestinal barrier function through the cytoskeletal association and expression of tight junction proteins in Caco-2 cells,” The Journal of Nutrition, vol. 141, no. 1, pp. 87–94, 2010. View at: Publisher Site | Google Scholar
  64. N. Ali and A.-E. Soheil, “A review of therapeutic effects of curcumin,” Current Pharmaceutical Design, vol. 19, no. 11, pp. 2032–2046, 2013. View at: Publisher Site | Google Scholar
  65. S. S. Ghosh, J. Bie, J. Wang, and S. Ghosh, “Oral supplementation with non-absorbable antibiotics or curcumin attenuates western diet-induced atherosclerosis and glucose intolerance in LDLR−/− mice – role of intestinal permeability and macrophage activation,” PLoS One, vol. 9, no. 9, article e108577, 2014. View at: Publisher Site | Google Scholar
  66. J. Wang, S. S. Ghosh, and S. Ghosh, “Curcumin improves intestinal barrier function: modulation of intracellular signaling, and organization of tight junctions,” American Journal of Physiology. Cell Physiology, vol. 312, no. 4, pp. C438–C445, 2017. View at: Publisher Site | Google Scholar
  67. C. Y. Kim and K.-H. Kim, “Curcumin prevents leptin-induced tight junction dysfunction in intestinal Caco-2 BBe cells,” The Journal of Nutritional Biochemistry, vol. 25, no. 1, pp. 26–35, 2014. View at: Publisher Site | Google Scholar
  68. B. Joe, M. Vijaykumar, and B. R. Lokesh, “Biological properties of curcumin-cellular and molecular mechanisms of action,” Critical Reviews in Food Science and Nutrition, vol. 44, no. 2, pp. 97–111, 2004. View at: Publisher Site | Google Scholar
  69. G. Yang, S. Bibi, M. Du, T. Suzuki, and M. J. Zhu, “Regulation of the intestinal tight junction by natural polyphenols: a mechanistic perspective,” Critical Reviews in Food Science and Nutrition, vol. 57, no. 18, pp. 3830–3839, 2017. View at: Publisher Site | Google Scholar

Copyright © 2018 Bonggi Lee et al. 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.

Related articles

No related content is available yet for this article.
 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

No related content is available yet for this article.

Article of the Year Award: Outstanding research contributions of 2021, as selected by our Chief Editors. Read the winning articles.