Review Article | Open Access
Nicole S. Olgun, Sandra E. Reznik, "The Matrix Metalloproteases and Endothelin-1 in Infection-Associated Preterm Birth", Obstetrics and Gynecology International, vol. 2010, Article ID 657039, 8 pages, 2010. https://doi.org/10.1155/2010/657039
The Matrix Metalloproteases and Endothelin-1 in Infection-Associated Preterm Birth
Preterm birth (PTB) is clinically defined as any delivery which occurs before the completion of 37 weeks of gestation, and is currently the most important problem in obstetrics. In the United States, PTB accounts for 12-13% of all live births, and, with the exception of fetuses suffering from anomalies, is the primary cause of perinatal mortality. While the risk factors for PTB are numerous, the single most common cause is intrauterine infection. As there is currently no FDA-approved therapy for infection-associated PTB, understanding the pathogenesis of preterm labor (PTL) and delivery should be given high priority. The matrix metalloproteinases (MMPs) are a family of enzymes that have been implicated in normal parturition as well as infection-triggered rupture of membranes and preterm birth. Several lines of evidence also suggest a role for endothelin-1 (ET-1) in infection-associated preterm delivery. This paper focuses on the evidence that the MMPs and ET-1 act in the same molecular pathway in preterm birth.
Preterm birth (PTB) is defined as any delivery occurring before the completion of 37 weeks of gestation, and currently accounts for 12-13% of all births in the United States. Despite advances that have been made in the field of neonatology and in our understanding of the mechanisms involved in parturition, the occurrence of PTB has not declined, and accounts for approximately 5,000 infant deaths in the United States per year . In 2005, the National Center for Health Statistics (Centers for Disease Control and Prevention) reported that there were 522,913 live preterm births in the United States, corresponding to a 20% increase (from 10.6% to 12.7%) in the number of women delivering prematurely, when compared to 1990 (http://www.marchofdimes.com/peristats/).
Babies born prematurely are at increased risk of having low birth weight (2,500 grams) and of perinatal mortality . While most deaths occur in babies born before 32 weeks of gestation, the biggest challenge arises when caring for those born at less than 28 weeks of gestational age. At this point, babies are considered to be of very low birth weight (VLBW), weighing 1,500 grams (3.33 lbs), and their organs are significantly less developed than those of those delivered at a later time. An estimated 6% of preterm babies are born before the completion of 28 weeks, while 71% are born between 34 and 36 weeks of gestation, and are referred to as “late preterm” [2–4].
The single most common cause of spontaneous PTB, aside from a previous premature delivery, is intrauterine infection in the mother (40%). Furthermore, the earlier on in the gestational time period at the time of delivery, the more likely it is that there is microbial infection in the amniotic cavity . Seen especially in infants born before the completion of 34 weeks of gestation, amniotic fluid (AF) infection is often coupled with a proinflammatory response noted by the presence of cytokines such as tumor necrosis factor-alpha (TNF-) and interleukin-6 (IL-6) . High levels of inflammatory cytokines have also been found in the cerebral spinal fluid of preterm infants, but appear to be independent of gestational age . Other risk factors for PTB include cervical or uterine abnormalities, lack of proper medical care, stress, smoking, and maternal age [1, 7].
In the clinical setting, inhibition of myometrial contractions (tocolysis) is the focus of therapeutic approaches for preventing PTB since the contracting uterus is the most commonly recognized precursor of an early delivery . Magnesium sulfate () is currently the tocolytic agent of choice, used by approximately 70% of responding medical personnel, followed by terbutaline (13%), nifedipine (11%), and indomethacin (6%). Interestingly, none of the drugs mentioned above have been proven to have a significant effect in adequately delaying gestation or in enhancing neonatal outcome [9–12].
Currently unavailable, a tocolytic agent would require the widespread documentation of its efficacy and safety, for both the mother and fetus. In the United States, and also abroad, recent guidelines have stressed the importance of the need to explore the postnatal consequences of infants exposed to tocolytic agents in utero. It is here that the importance of nonclinical animal studies becomes evident as they are needed to investigate the findings which cannot be ethically, sufficiently, and/or safely determined with pediatric clinical trials [13–15].
2. The Pathway Leading to Preterm Birth
As mentioned previously, maternal infection is one of the leading causes of PTB, and is the only pathological process for which there is a direct causal relationship with prematurity . However, despite a vast accumulation of human and animal data, the exact pathways and mechanisms leading to this point remain incompletely understood.
While systemic maternal infections such as malaria and pneumonia can cause PTB, the occurrences of these infections are minimal in developed countries. Instead, the majority of infections leading to premature labor is often those which are intrauterine . Unfortunately, the diagnosis of such types of infections early on in gestation is complicated. This can be attributed to the fact that the most tell-tale clinical signs of infection, which include fever, tenderness of the uterus, fetal tachycardia, and so forth, tend to occur late in the process of evolving infection, and do not present in a large percent of women, despite evidence that microorganisms are present in the amniotic cavity . Mothers with infection of the amniotic cavity may not respond as well to treatment with tocolytics due to the presence of underlying inflammation [18, 19].
The most common route by which infection occurs is via the ascension of microorganisms from the vagina and cervix through the chorioamniotic membranes and into the amniotic cavity, where it will eventually cause infection in the fetus. As a result, a fetal inflammatory response may develop, most commonly denoted by funisitis (inflammation of the umbilical cord) which has been associated with the development of cerebral palsy [17, 20, 21].
The noted presence of bacteria and infection in the gestational compartment and other areas of pregnant women have been shown to trigger the immune system via cell surface recognition molecules such as toll-like receptors (TLRs) . TLRs are transmembrane proteins capable of recognizing and responding to precise patterns of microbial components, and initiate the innate immune system in the host against nonself [23, 24].
Currently, 12 TLRs have been identified in mammals. In particular, TLR-2 recognizes Gram-positive bacteria while TLR-4 recognizes Gram-negative organisms and binds to lipopolysaccharide (LPS) [25–27]. LPS is a component of the outer wall of Gram-negative bacteria and is often used to stimulate an immune response in the animal model. Except for TLR-3, binding of mammalian TLRs activates the MyD88- (myeloid differentiation primary-response genes 88-) dependant pathway, which, in turn, activates the transcription factor nuclear factor-. NF- has been implicated in eliciting the expression of proinflammatory genes which play a role in PTB [24, 28, 29].
In humans, the binding of TLR-4 initiates a host inflammatory response involving cytokines such as IL-1 and TNF, thus playing a critical role in the pathogenesis of infection-associated PTB [30–32]. The inflammatory response is responsible for inducing steps in the latter part of the parturition cascade, such as decreased prostaglandin catabolism, functional progesterone withdrawal, increased expression of proteases, contraction-associated proteins, and increased uterine contractile activity, ultimately leading to labor and delivery .
3. Matrix Metalloproteinases
During pregnancy, specific physiological processes such as cervical ripening, rupture of the fetal membranes, and placental detachment require the remodeling of the extracellular matrix (ECM) [33–37]. Rupturing of the membranes is believed to be the result of the effects of physical forces which are localized in areas surrounding the membranes that are made weaker by the degradation of structural collagens . The matrix metalloproteinases (MMPs) are a family of enzymes (with more than 20 members identified) that use zinc-dependant catalysis to break down the components of the ECM , allowing for the movement of cells and tissue reorganization in order to support the growing fetus . Several MMPs are constitutively generated by reproductive tissues, and a fluctuation in the gene expression level of certain MMPs has been observed during the various stages of parturition .
The ECM of the cervix, fetal membranes, placenta, and uterus are composed mainly of collagen types I and III. Investigators have shown that a remodeling of these collagens, mediated by the MMPs, may play a role in the pathway leading to birth . A spontaneous rupturing of membranes before the completion of 37 weeks of gestation is considered to be of pathological origin and is a leading cause of PTB and delivery . The MMPs are also believed to play a major role in the remodeling of the uteroplacental vasculature which changes throughout pregnancy .
Several lines of investigation have implicated specific MMPs in normal parturition as well as infection-triggered rupture of membranes and preterm birth. A cross-sectional study conducted by Maymon et al.  reported that, out of 353 women involved, concentrations of MMP-1 were detectable in 81.3% of amniotic fluid samples, with the concentrations increasing with gestational age. Additionally, preterm PROM was associated with a significant increase in the median concentrations of amniotic MMP-1 in both the presence and absence of infection, while term PROM was not associated with an increase in MMP-1 levels . Interestingly, Fujimoto et al. found that a polymorphism resulting in increased MMP-1 promoter activity resulted in an increased risk of preterm premature rupture of the membranes . In a cross-sectional study involving 365 subjects and conducted by Park et al. , increased levels of MMP-3 were associated with parturition, both term and preterm, as wells as microbial invasion of the amniotic cavity.
Recently, much attention has been given to MMP-9, also known as 92-kDa type IV collagenase or gelatinase B . MMP-9 is considered to be an enzyme which plays a role in the latter part of ECM remodeling and, unlike other MMPs, is produced and activated under certain conditions such as infection, active labor, and premature rupture of the membranes (PROM) [46, 47]. In the setting of intraamniotic infection, the concentrations of AF MMP-9 and the inflammatory cytokine IL-6 have been found to be significantly elevated . A study conducted by Harirah et al.  reported that 22 out of 26 women with positive AF cultures had detectable levels of MMP-9, ranging from 30.1 to 541.9 ng/mL, while MMP-9 was nearly undetectable in women with negative AF cultures. The MMP-9 cutoff value used for predicting the presence or absence of infection was 13.6 ng/mL. In this study, spontaneous PTB was not explored as an outcome because, for the majority of women, the benefits of inducing labor or having a cesarean delivery outweighed those of going on with their pregnancies.
In women with normal pregnancies, elevated levels of MMP-9 have been found in the cervicovaginal fluid and are associated with cervical ripening before labor, but are not a useful predictor for labor induction at term . Under certain conditions, cervical ripening can be induced by the inflammatory process which involves the catabolism of the cervical ECM by enzymes discharged from infiltrating leukocytes . Watari et al.  reported that, in a dose-dependent manner, the inflammatory cytokines TNF- and IL-1, which have been associated with PTB, produce an increase in MMPs-1, -3, and -9 in a human uterine smooth muscle system. Interestingly, these MMPs are the only ones to have promoters that contain Activator Protein-1 and Ets-binding sites .
While MMP-9 has been found to play a role in the events associated with term and preterm labor, comparable changes in MMP-2 protein levels and activity are often not reported. This may suggest that MMP-2 is expressed continuously throughout labor  while MMP-9 expression is induced by various factors as previously mentioned. On the other hand, Yonemoto et al.  have also reported, in 2005, on the gestational age-dependant increases in MMP-2 proenzyme activity and protein levels from the amnion in patients in labor, suggestive of the induction of enzyme expression later on in gestation. Moreover, Maymon et al. (2001) found a decrease in tissue inhibitor of matrix metalloproteinase-2 (TIMP-2) in association with term and preterm parturition, term and preterm rupture of fetal membranes, and microbial invasion of the amniotic cavity .
An increase in midtrimester concentrations of amniotic fluid MMP-8, IL-6, and angiogenin are risk factors for early spontaneous preterm delivery (32 weeks). MMP-8 is released during neutrophil activation, and amniotic fluid concentrations are elevated both in patients with intraamniotic infection and in patients with negative amniotic fluid cultures who deliver preterm. Yoon et al.  have developed a rapid MMP-8 bedside test that predicts imminent preterm delivery. This test can be performed in 15 minutes and without laboratory equipment. In particular, an elevated MMP-8 level of 23 ng/mL is a powerful predictor of spontaneous preterm delivery (32 weeks). Amniotic fluid studies can be used to improve the risk assessment for preterm delivery in women who undergo midtrimester amniocentesis for genetic indications .
Even though some of the best clinical predictors for PTL include cervical dilation 3 cm, vaginal bleeding, and ruptured membranes, these changes often appear too late for successful intervention . However, the detection of plasma pro-MMP-9 levels and measurement of cervical length in combination with cutoff values of 65.157 ng/mL and 15 mm, respectively, are characterized by 90.9% sensitivity and 98.3% specificity and have been shown to possibly function as predictive factors for PTB and PTL within 7 days of presentation.
We have recently shown, using cDNA microarray technology, that several genes related to ECM homeostasis are upregulated in placental chorionic villi from patients who have labored as compared to patients who have undergone Cesarean deliveries without labor . In particular, we found that MMP-1 was consistently elevated in placentas from patients who had labored as compared to placentas from patients who had not labored at both the mRNA and protein level. Interestingly, the upregulation in MMP-1 was seen in the fetal portion of the placenta, suggesting that the fetus can contribute to its own premature expulsion from a hostile intrauterine environment.
In 2007, we tested the nonspecific MMP inhibitor GM6001 (EMD Biosciences, La Jolla, CA) for its effect on endotoxin-triggered preterm labor in a mouse model . GM6001 has values for MMP-1, -2, -3, -8, and -9 which are in the nanomolar-to-picomolar range. Briefly, pregnant C57Bl/6 mice were injected with LPS on gestational days 15.5–16 in order to simulate infection-associated PTB and then received either GM6001 (study group) or vehicle (control group) 12 hours later. In the GM6001 group there was a significant decrease in the number of mice delivering prematurely when compared to the controls (Figure 1), suggesting that one or more of the MMPs are critical in the pathogenesis of infection-associated PTB.
4. The Endothelins
The human endothelin (ET) peptide family is made up of three distinct isoforms—ET-1, ET-2, and ET-3 . Composed of 21 amino acid residues with two sets of intrachain disulfide linkages, the endothelins are produced in an array of tissues with different distribution patterns and regulate vasomotor tone, cell proliferation, and hormone production [55–57].
Two types of ET receptors, Endothelin-A () and Endothelin-B (), have been identified in most mammalian species and belong to the superfamily of G-protein-coupled receptors (GPCRs) . Even though their amino acid structures exhibit a significant amount of similar homology, the receptors have varying affinities for the three ET isoforms . While the receptor has a much greater affinity for ET-1 as compared to ET-2 and ET-3, the receptor binds all three members with equal affinity .
ET-1 is the most potent vasoconstrictor in the ET family, exhibiting a long duration of action, and is also the only member to be produced in endothelial cells . ET can induce vasoconstriction via two major cell signaling systems: the opening of calcium () channels and phospholipase-C activation . Additionally, ET-1 is also produced by a broad spectrum of cell types, including vascular smooth muscle cells, hepatocytes, breast epithelial cells, and astrocytes of the central nervous system .
The 203-amino acid residue peptide precursor preproendothelin-1 gives rise to ET-1 via the formation of the 38- or 39- (species-dependent) amino acid intermediate termed “big ET-1” which circulates in plasma . Interestingly, big ET-1 is significantly less potent than ET-1 in terms of inducing contractile actions in vascular strips, but both forms are equally potent in raising blood pressure in vivo .
Endothelin-converting enzyme-1 (ECE-1) is responsible for the cleaving of big ET-1 between the Trp21 and Val22 residues, ultimately leading to the formation of ET-1 . ET-1 is now implicated in an ever-growing list of pathologic processes, ranging from pulmonary hypertension to cancer. In particular, several lines of evidence support the involvement of the peptide in obstetrical disorders. An increase in maternal plasma ET-1 levels in patients with preeclampsia was first noted in 1990 . Because the receptor has such a great affinity for ET-1, the possible therapeutic benefit of selective receptor antagonists in preeclamptic women needs to be further explored. Furthermore, receptor-directed therapy may overlap with antihypertensive management in preeclamptic patients. The usefulness of this approach remains uninvestigated .
Several investigators found that, in pregnant rats, a chronic elevation in the serum levels of TNF- and IL-6 and a reduction in uterine perfusion pressure lead to the activation of the ET system [62, 63]. Romero et al. found higher human amniotic fluid concentrations of ET-1, -2 among women who developed preterm labor and delivery and had culture-proven microbial invasion of the amniotic cavity  as compared to uninfected women, suggesting a role for the endothelins in infection-associated preterm birth. Mitchell et al. reported that ET-1 regulates prostaglandin production in human umbilical vein endothelial cells and cells derived from the amnion and decidua .
We reported in 2004 that inhibition of endothelin-converting enzyme-1 (ECE-1), which colocalizes with ET-1 in the placenta , controls PTD in a mouse model of infection-associated PTL . Subsequently, we have shown that ECE-1 is upregulated in our mouse model of PTL and that PTD is controlled with the receptor antagonist BQ-123 and with silencing of ECE-1 mRNA  (Figure 2).
Investigators have previously shown that, when compared to ET-1, the responsiveness of the rat uterus to the contractile effects of ET-3 is less than 1%, suggesting that the receptor is responsible for modulating uterine contractions . Therefore, our group has recently developed a series of novel receptor antagonists. We have shown that one of our compounds, HJP-272, a 1, 3, 6-trisubstituted-2-carboxy-quinol-4-one (IC50, 70 nmol/L), is capable of significantly decreasing the number of pups that are dropped prematurely in the setting of infection .
While we do know that ET plays a very important role in the inflammatory cascade-associated infection-induced PTB, the use of receptor antagonists as a form of tocolytic therapy remains controversial. Bosentan, often used in the treatment of pulmonary hypertension, is a dual ET receptor antagonist approved for use in the United States. While the use of ET receptor antagonists may be useful for the treatment of pulmonary hypertension, these agents are often disregarded as potential tocolytics due to the fact that most are pregnancy Category X drugs.
5. The Link between ET-1 and the MMPs
Recently, we have tested whether endothelin-1 and MMP-1 act in the same molecular pathway in our mouse model of infection-associated preterm birth. We have shown that MMP-1 is upregulated in placental and uterine tissues of mice induced to preterm labor and delivery with LPS (manuscript submitted for publication) and that the MMP inhibitor GM6001 controls preterm birth in these same animal models. We also compared levels of MMP-1 in LPS-induced mice that were treated with RNAi directed at ECE-1 to levels of the protein in positive control LPS-induced mice with unaltered ET-1 systems. We were interested to find that knocking down ET-1 synthesis knocked down MMP-1 upregulation as well. Furthermore, those mice in which ECE-1 and, consequently, MMP-1 levels were reduced were largely prevented from developing preterm delivery (manuscript submitted).
Several lines of investigation in other biologic systems have established that ET-1 affects the synthesis of MMPs. Koyama and Tanaka  have recently shown that ET-1 stimulates the production of MMP-3 in cultured rat astrocytes. Similarly, Manacu et al.  found that, in primary cultures of human osteoarthritic chondrocytes, the presence of ET-1 in the medium triggered increased production of MMP-1 and MMP-13. Felx et al.  found that ET-1 promotes induction of MMP-2 and MMP-9 in human osteosarcoma cells via the transcription factor NF-κ. Furthermore, treatment of these malignant cells with ET receptor antagonists decreases cell invasion. In ET-1-activated human optic nerve head astrocytes, levels of MMP-1, TIMP-1, and TIMP-2 are all increased. These changes are mediated through the ERK map kinases and protein kinase C . ET-1 promotes cerebrovascular remodeling in type 2 diabetes through differential regulation of MMPs . Murray et al.  produced a marked increase in MMP-2 activity and a significant decrease in collagen volume fraction in rat hearts by administering ET-1. More recently, they have shown that rats that underwent the surgical introduction of an aortocaval fistula had much less of a change in MMP-2 levels and in collagen volume fraction of the heart if they were treated with Bosentan, an endothelin receptor antagonist . Interestingly, Lee et al. reported that vascular endothelial growth factor- (VEGF-) induced ET-1 production occurs via MMP-2 action, and independently of ECE-1 function . Finally, Deschamps et al.  showed that the increase in MMP-1 levels in porcine hearts associated with ischemia and reperfusion injury did not occur if the animals were treated with the ET-1 receptor-A antagonist BQ-123.
Increased levels of inflammatory cytokines in the setting of infection ultimately lead to PTL and PTB via several different mechanisms and feedback loops which occur at the maternal fetal interface. Several lines of evidence indicate that both ET-1 and the MMPs are critical parts of the molecular pathway that connects ascending bacterial infection to PTB. A simple skeletal version of the parturition cascade, including the putative sites of activity of ET-1 and the MMPs, is shown in Figure 3. On one hand, the risk of teratogenicity caused by any potential tocolytic agent is minimized, because the period of administration is transient, and because the agent would be given well after organogenesis is complete. On the other hand, as both endothelin and the MMPs play a role in embryonic and fetal development, agents blocking the actions of either of these important molecular players are somewhat suspect for potential fetal toxicity. A better understanding of the infection-associated preterm labor molecular pathway is needed, so that more and more potential targets for therapy can be revealed.
- C. J. Lockwood, “Predicting premature delivery—no easy task,” The New England Journal of Medicine, vol. 346, no. 4, pp. 282–284, 2002.
- S. J. Ventura, J. A. Martin, S. C. Curtin, and T. J. Mathews, “Report of final natality statistics, 1996,” Monthly Vital Statistics Report, vol. 46, no. 11, pp. 1–99, 1998.
- D. O. Anumba, “Management of women with a previous preterm birth,” Obstetrics, Gynaecology and Reproductive Medicine, vol. 17, no. 6, pp. 188–191, 2007.
- J. A. Martin, B. E. Hamilton, P. D. Sutton, S. J. Ventura, F. Menacker, and S. Kirmeyer, “Births: final data for 2004,” National Vital Statistics Reports, vol. 55, no. 1, pp. 1–101, 2006.
- D. H. Watts, M. A. Krohn, S. L. Hillier, and D. A. Eschenbach, “The association of occult amniotic fluid infection with gestational age and neonatal outcome among women in preterm labor,” Obstetrics and Gynecology, vol. 79, no. 3, pp. 351–357, 1992.
- M. A. Turner, J. A. Drury, and J. A. Drury, “CSF cytokine levels in preterm infants may reflect systemic inflammation and are independent of gestation,” Early Human Development, vol. 85, no. 4, pp. 259–262, 2009.
- J. D. Iams, “The epidemiology of preterm birth,” Clinics in Perinatology, vol. 30, no. 4, pp. 651–664, 2003.
- H. N. Simhan and S. N. Caritis, “Prevention of preterm delivery,” The New England Journal of Medicine, vol. 357, no. 5, pp. 477–442, 2007.
- C. A. Crowther, J. E. Hiller, and L. W. Doyle, “Magnesium sulphate for preventing preterm birth in threatened preterm labour,” Cochrane Database of Systematic Reviews, no. 4, Article ID CD001060, 2002.
- E. Hayes, L. Moroz, L. Pizzi, and J. Baxter, “A cost decision analysis of 4 tocolytic drugs,” American Journal of Obstetrics and Gynecology, vol. 197, no. 4, pp. 383e1–383e6, 2007.
- M. L. McPheeters, W. C. Miller, K. E. Hartmann, D. A. Savitz, J. S. Kaufman, J. M. Garrett, and J. M. Thorp, “The epidemiology of threatened preterm labor: a prospective cohort study,” American Journal of Obstetrics and Gynecology, vol. 192, no. 4, pp. 1325–1330, 2005.
- E. R. Norwitz, M. O. Bahtiyar, and B. M. Sibai, “Defining standards of care in maternal-fetal medicine,” American Journal of Obstetrics and Gynecology, vol. 191, no. 4, pp. 1491–1496, 2004.
- A. D. Rasmussen, J. K. Nelson, G. J. Chellman, M. Golub, and P. A. McAnulty, “Use of barusiban in a novel study design for evaluation of tocolytic agents in pregnant and neonatal monkeys, including behavioural and immunological endpoints,” Reproductive Toxicology, vol. 23, no. 4, pp. 471–479, 2007.
- EMEA, “Guideline on the need for non-clinical testing in juvenile animals of pharmaceuticals for paediatric indications,” August 2008.
- FDA, “Guidance for industry: immunotoxicology evaluation of investigational new drugs,” 2002.
- R. Gomez, R. Romero, M. Mazor, F. Ghezzi, C. David, and B. H. Yoon, “Role of infection in preterm labor and delivery,” in Preterm Labor, R. F. Lamont, Ed., pp. 85–125, Churchill Livingstone, New York, NY, USA, 1997.
- R. Romero, J. Espinoza, T. Chaiworapongsa, and K. Kalache, “Infection and prematurity and the role of preventive strategies,” Seminars in Neonatology, vol. 7, no. 4, pp. 259–274, 2002.
- A. Y. El-Bastawissi, M. A. Williams, J. Hitti, and J. N. Krieger, “Amniotic fluid interleukin-6 and preterm delivery: a review,” Obstetrics and Gynecology, vol. 95, no. 6, pp. 1056–1064, 2000.
- C. Hameed, N. Tejani, U. L. Verma, and F. Archbald, “Silent chorioamnionitis as a cause of preterm labor refractory to tocolytic therapy,” American Journal of Obstetrics and Gynecology, vol. 149, no. 7, pp. 726–730, 1984.
- C.-W. Park, K. C. Moon, J. S. Park, J. K. Jun, R. Romero, and B. H. Yoon, “The involvement of human amnion in histological chorioamnionitis is an indicator that a fetal and an intra-amniotic inflammatory response is more likely and severe: clinical implications,” Placenta, vol. 30, no. 1, pp. 56–61, 2009.
- B. H. Yoon, R. Romero, J. S. Park, C. J. Kim, S. H. Kim, J.-H. Choi, and T. R. Han, “Fetal exposure to an intra-amniotic inflammation and the development of cerebral palsy at the age of three years,” American Journal of Obstetrics and Gynecology, vol. 182, no. 3, pp. 675–681, 2000.
- E. Hirsch and H. Wang, “The molecular pathophysiology of bacterially induced preterm labor: insights from the murine model,” Journal of the Society for Gynecologic Investigation, vol. 12, no. 3, pp. 145–155, 2005.
- K. Takeda, T. Kaisho, and S. Akira, “Toll-like receptors,” Annual Review of Immunology, vol. 21, pp. 335–376, 2003.
- Y. Filipovich, S.-J. Lu, S. Akira, and E. Hirsch, “The adaptor protein MyD88 is essential for E coli-induced preterm delivery in mice,” American Journal of Obstetrics and Gynecology, vol. 200, no. 1, pp. 93e1–93e8, 2009.
- A. Poltorak, X. He, and X. He, “Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice: mutations in Tlr4 gene,” Science, vol. 282, no. 5396, pp. 2085–2088, 1998.
- S. T. Qureshi, L. Larivière, G. Leveque, S. Clermont, K. J. Moore, P. Gros, and D. Malo, “Endotoxin-tolerant mice have mutations in Toll-like receptor 4 (Tlr4),” Journal of Experimental Medicine, vol. 189, no. 4, pp. 615–625, 1999.
- O. Takeuchi, K. Hoshino, and K. Hoshino, “Differential roles of TLR2 and TLR4 in recognition of gram-negative and gram-positive bacterial cell wall components,” Immunity, vol. 11, no. 4, pp. 443–451, 1999.
- M. Lappas, M. Permezel, H. M. Georgiou, and G. E. Rice, “Nuclear factor Kappa B regulation of proinflammatory cytokines in human gestational tissues in vitro,” Biology of Reproduction, vol. 67, no. 2, pp. 668–673, 2002.
- A. R. Belt, J. J. Baldassare, M. Molnár, R. Romero, and F. Hertelendy, “The nuclear transcription factor NF-κB mediates interleukin-1β-induced expression of cyclooxygenase-2 in human myometrial cells,” American Journal of Obstetrics and Gynecology, vol. 181, no. 2, pp. 359–366, 1999.
- D. J. Dudley, D. Collmer, M. D. Mitchell, and M. S. Trautman, “Inflammatory cytokine mRNA in human gestational tissues: implications for term and preterm labor,” Journal of the Society for Gynecologic Investigation, vol. 3, no. 6, pp. 328–335, 1996.
- R. Romero, M. Mazor, F. Brandt, W. Sepulveda, C. Avila, D. B. Cotton, and C. A. Dinarello, “Interleukin-1α and interleukin-1β in preterm and term human parturition,” American Journal of Reproductive Immunology, vol. 27, no. 3-4, pp. 117–123, 1992.
- R. Romero, M. Mazor, W. Sepulveda, C. Avila, D. Copeland, and J. Williams, “Tumor necrosis factor in preterm and term labor,” American Journal of Obstetrics and Gynecology, vol. 166, no. 5, pp. 1576–1587, 1992.
- M. R. Rajabi, D. D. Dean, S. N. Beydoun, and J. F. Woessner Jr., “Elevated tissue levels of collagenase during dilation of uterine cervix in human parturition,” American Journal of Obstetrics and Gynecology, vol. 159, no. 4, pp. 971–976, 1988.
- F. Vadillo-Ortega and G. Estrada-Gutiérrez, “Role of matrix metalloproteinases in preterm labour,” BJOG, vol. 112, no. s1, pp. 19–22, 2005.
- D. Draper, J. McGregor, J. Hall, W. Jones, M. Beutz, R. P. Heine, and R. Porreco, “Elevated protease activities in human amnion and chorion correlate with preterm premature rupture of membranes,” American Journal of Obstetrics and Gynecology, vol. 173, no. 5, pp. 1506–1512, 1995.
- D. Tsatas, M. S. Baker, and G. E. Rice, “Differential expression of proteases in human gestational tissues before, during and after spontaneous-onset labour at term,” Journal of Reproduction and Fertility, vol. 116, no. 1, pp. 43–49, 1999.
- H. Yonemoto, C. B. Young, J. T. Ross, L. L. Guilbert, R. J. Fairclough, and D. M. Olson, “Changes in matrix metalloproteinase (MMP)-2 and MMP-9 in the fetal amnion and chorion during gestation and at term and preterm labor,” Placenta, vol. 27, no. 6-7, pp. 669–677, 2006.
- E. Maymon, R. Romero, P. Pacora, M.-T. Gervasi, K. Bianco, F. Ghezzi, and B. H. Yoon, “Evidence for the participation of interstitial collagenase (matrix metalloproteinase 1) in preterm premature rupture of membranes,” American Journal of Obstetrics and Gynecology, vol. 183, no. 4, pp. 914–920, 2000.
- H. Harirah, S. E. Donia, and C.-D. Hsu, “Amniotic fluid matrix metalloproteinase-9 and interleukin-6 in predicting intra-amniotic infection,” Obstetrics and Gynecology, vol. 99, no. 1, pp. 80–84, 2002.
- B. A. Kelly, B. C. Bond, and L. Poston, “Gestational profile of matrix metalloproteinases in rat uterine artery,” Molecular Human Reproduction, vol. 9, no. 5-6, pp. 351–358, 2003.
- G. D. Bryant-Greenwood and S. Y. Yamamoto, “Control of peripartal collagenolysis in the human chorion-decidua,” American Journal of Obstetrics and Gynecology, vol. 172, no. 1, pp. 63–70, 1995.
- F. Vadillo-Ortega, G. Gonzalez-Avila, E. E. Furth, H. Lei, R. J. Muschel, W. G. Stetler-Stevenson, and J. F. Strauss III, “92-kd type IV collagenase (matrix metalloproteinase-9) activity in human amniochorion increases with labor,” American Journal of Pathology, vol. 146, no. 1, pp. 148–156, 1995.
- G. Opdenakker, “On the roles of extracellular matrix remodeling by gelatinase B,” Verhandelingen-Koninklijke Academie voor Geneeskunde van België, vol. 59, no. 6, pp. 489–514, 1997.
- T. Fujimoto, S. Parry, and S. Parry, “A single nucleotide polymorphism in the matrix metalloproteinase-1 (MMP-1) promoter influences amnion cell MMP-1 expression and risk for preterm premature rupture of the fetal membranes,” Journal of Biological Chemistry, vol. 277, no. 8, pp. 6296–6302, 2002.
- K. H. Park, T. Chaiworapongsa, and T. Chaiworapongsa, “Matrix metalloproteinase 3 in parturition, premature rupture of the membranes, and microbial invasion of the amniotic cavity,” Journal of Perinatal Medicine, vol. 31, no. 1, pp. 12–22, 2003.
- S. J. Fortunato, R. Menon, and S. J. Lombardi, “Collagenolytic enzymes (gelatinases) and their inhibitors in human amniochorionic membrane,” American Journal of Obstetrics and Gynecology, vol. 177, no. 4, pp. 731–741, 1997.
- S.-J. Choi, K.-L. Jung, S.-Y. Oh, J.-H. Kim, and C.-R. Roh, “Cervicovaginal matrix metalloproteinase-9 and cervical ripening in human term parturition,” European Journal of Obstetrics Gynecology and Reproductive Biology, vol. 142, no. 1, pp. 43–47, 2009.
- P. Xu, N. Alfaidy, and J. R. G. Challis, “Expression of matrix metalloproteinase (MMP)-2 and MMP-9 in human placenta and fetal membranes in relation to preterm and term labor,” Journal of Clinical Endocrinology and Metabolism, vol. 87, no. 3, pp. 1353–1361, 2002.
- M. Watari, H. Watari, M. E. DiSanto, S. Chacko, G.-P. Shi, and J. F. Strauss III, “Pro-inflammatory cytokines induce expression of matrix-metabolizing enzymes in human cervical smooth muscle cells,” American Journal of Pathology, vol. 154, no. 6, pp. 1755–1762, 1999.
- E. Maymon, R. Romero, and R. Romero, “A role for the 72 kDa gelatinase (MMP-2) and its inhibitor (TIMP-2) in human parturition, premature rupture of membranes and intraamniotic infection,” Journal of Perinatal Medicine, vol. 29, no. 4, pp. 308–316, 2001.
- B. H. Yoon, S.-Y. Oh, R. Romero, S.-S. Shim, S.-Y. Han, J. S. Park, and J. K. Jun, “An elevated amniotic fluid matrix metalloproteinase-8 level at the time of mid-trimester genetic amniocentesis is a risk factor for spontaneous preterm delivery,” American Journal of Obstetrics and Gynecology, vol. 185, no. 5, pp. 1162–1167, 2001.
- J. McLaren, T. M. Malak, and S. C. Bell, “Structural characteristics of term human fetal membranes prior to labour: identification of an area of altered morphology overlying the cervix,” Human Reproduction, vol. 14, no. 1, pp. 237–241, 1999.
- T.-D. Vu, Y. Feng, J. Placido, and S. E. Reznik, “Placental matrix metalloproteinase-1 expression is increased in labor,” Reproductive Sciences, vol. 15, no. 4, pp. 420–424, 2008.
- K. L. Koscica, C. V. Ananth, J. Placido, and S. E. Reznik, “The effect of a matrix metalloproteinase inhibitor on inflammation-mediated preterm delivery,” American Journal of Obstetrics and Gynecology, vol. 196, no. 6, pp. 551.e1–551.e3, 2007.
- M. Yanagisawa, H. Kurihara, and H. Kurihara, “A novel potent vasoconstrictor peptide produced by vascular endothelial cells,” Nature, vol. 332, no. 6163, pp. 411–415, 1988.
- G. M. Rubanyi and M. A. Polokoff, “Endothelins: molecular biology, biochemistry, pharmacology, physiology, and pathophysiology,” Pharmacological Reviews, vol. 46, no. 3, pp. 325–415, 1994.
- M. S. Simonson, “Endothelins: multifunctional renal peptides,” Physiological Reviews, vol. 73, no. 2, pp. 375–412, 1993.
- T. Sakurai, M. Yanagisawa, and T. Masaki, “Molecular characterization of endothelin receptors,” Trends in Pharmacological Sciences, vol. 13, no. 3, pp. 103–108, 1992.
- E. R. Levin, “Endothelins,” The New England Journal of Medicine, vol. 333, no. 6, pp. 356–363, 1995.
- R. N. Taylor, M. Varma, N. N. H. Teng, and J. M. Roberts, “Women with preeclampsia have higher plasma endothelin levels than women with normal pregnancies,” Journal of Clinical Endocrinology and Metabolism, vol. 71, no. 6, pp. 1675–1677, 1990.
- B. D. LaMarca, B. T. Alexander, J. S. Gilbert, M. J. Ryan, M. Sedeek, S. R. Murphy, and J. P. Granger, “Pathophysiology of hypertension in response to placental ischemia during pregnancy: a central role for endothelin?” Gender Medicine, vol. 5, no. 1, pp. S133–S138, 2008.
- B. Babbette, D. LaMarca, W. A. Bennett, B. T. Alexander, K. Cockrell, and J. P. Granger, “Hypertension produced by reductions in uterine perfusion in the pregnant rat: role of tumor necrosis factor-alpha,” Hypertension, vol. 46, no. 4, pp. 1022–1025, 2005.
- G. Gadonski, B. B. D. LaMarca, E. Sullivan, W. Bennett, D. Chandler, and J. P. Granger, “Hypertension produced by reductions in uterine perfusion in the pregnant rat: role of interleukin 6,” Hypertension, vol. 48, no. 4, pp. 711–716, 2006.
- R. Romero, C. Avila, S. S. Edwin, and M. D. Mitchell, “Endothelin-1,2 levels are increased in the amniotic fluid of women with preterm labor and microbial invasion of the amniotic cavity,” American Journal of Obstetrics and Gynecology, vol. 166, no. 1, pp. 95–99, 1992.
- M. D. Mitchell, R. J. Romero, R. Lepera, L. Rittenhouse, and S. S. Edwin, “Actions of endothelin-1 on prostaglandin production by gestational tissues,” Prostaglandins, vol. 40, no. 6, pp. 627–635, 1990.
- Z. Ahmad and S. E. Reznik, “Immunohistochemical localization of ECE-1 in the human placenta,” Placenta, vol. 21, no. 2-3, pp. 226–233, 2000.
- K. L. Koscica, G. Sylvestre, and S. E. Reznik, “The effect of phosphoramidon on inflammation-mediated preterm delivery in a mouse model,” American Journal of Obstetrics and Gynecology, vol. 190, no. 2, pp. 528–531, 2004.
- W. Wang, H. Yen, C.-H. Chen, R. Soni, N. Jasani, G. Sylvestre, and S. E. Reznik, “The endothelin-converting enzyme-1/endothelin-1 pathway plays a critical role in inflammation-associated premature delivery in a mouse model,” American Journal of Pathology, vol. 173, no. 4, pp. 1077–1084, 2008.
- C. Yallampalli and R. E. Garfield, “Uterine contractile responses to endothelin-1 and endothelin receptors are elevated during labor,” Biology of Reproduction, vol. 51, no. 4, pp. 640–645, 1994.
- N. Olgun, H. J. Patel, R. Stephani, W. Wang, H. Yen, and S. E. Reznik, “Effect of the putative novel selective -receptor antagonist HJP272, a 1,3,6-trisubstituted-2-carboxy-quinol-4-one, on infection-mediated premature delivery,” Canadian Journal of Physiology and Pharmacology, vol. 86, no. 8, pp. 571–575, 2008.
- Y. Koyama and K. Tanaka, “Endothelins stimulate the production of stromelysin-1 in cultured rat astrocytes,” Biochemical and Biophysical Research Communications, vol. 371, no. 4, pp. 659–663, 2008.
- C. A. Manacu, J. Martel-Pelletier, and J. Martel-Pelletier, “Endothelin-1 in osteoarthritic chondrocytes triggers nitric oxide production and upregulates collagenase production,” Arthritis Research & Therapy, vol. 7, no. 2, pp. R324–R332, 2005.
- M. Felx, M.-C. Guyot, and M.-C. Guyot, “Endothelin-1 (ET-1) promotes MMP-2 and MMP-9 induction involving the transcription factor NF-B in human osteosarcoma,” Clinical Science, vol. 110, no. 6, pp. 645–654, 2006.
- S. He, G. Prasanna, and T. Yorio, “Endothelin-1-mediated signaling in the expression of matrix metalloproteinases and tissue inhibitors of metalloproteinases in astrocytes,” Investigative Ophthalmology and Visual Science, vol. 48, no. 8, pp. 3737–3745, 2007.
- A. K. Harris, J. R. Hutchinson, and J. R. Hutchinson, “Type 2 diabetes causes remodeling of cerebrovasculature via differential regulation of matrix metalloproteinases and collagen synthesis: role of endothelin-1,” Diabetes, vol. 54, no. 9, pp. 2638–2644, 2005.
- D. B. Murray, J. D. Gardner, G. L. Brower, and J. S. Janicki, “Effects of nonselective endothelin-1 receptor antagonism on cardiac mast cell-mediated ventricular remodeling in rats,” American Journal of Physiology, vol. 294, no. 3, pp. H1251–H1257, 2008.
- D. B. Murray, J. D. Gardner, G. L. Brower, and J. S. Janicki, “Endothelin-1 mediates cardiac mast cell degranulation, matrix metalloproteinase activation, and myocardial remodeling in rats,” American Journal of Physiology, vol. 287, no. 5, pp. H2295–H2299, 2004.
- K.-J. Lee, M.-K. Kim, Y.-H. Park, H.-J. Seol, J.-E. Lim, J. N. Lee, and M.-J. Oh, “Vascular endothelial growth factor induces endothelin-1 production via matrix metalloproteinase-2 rather than endothelin-converting enzyme-1,” Hypertension in Pregnancy, vol. 26, no. 2, pp. 189–199, 2007.
- A. M. Deschamps, J. Zavadzkas, and J. Zavadzkas, “Interruption of endothelin signaling modifies membrane type 1 matrix metalloproteinase activity during ischemia and reperfusion,” American Journal of Physiology, vol. 294, no. 2, pp. H875–H883, 2008.
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