- Research article
- Open Access
- Open Peer Review
Prostaglandin pathway gene expression in human placenta, amnion and choriodecidua is differentially affected by preterm and term labour and by uterine inflammation
© Phillips et al.; licensee BioMed Central Ltd. 2014
- Received: 29 November 2013
- Accepted: 15 July 2014
- Published: 22 July 2014
Elucidation of the biochemical pathways involved in activation of preterm and term human labour would facilitate the development of effective management and inform judgements regarding the necessity for preterm tocolysis and post-term induction. Prostaglandins act at all stages of human reproduction, and are potentially activators of labour.
Expression of 15 genes involved in prostaglandin synthesis, transport and degradation was measured by qPCR using tissue samples from human placenta, amnion and choriodecidua at preterm and full-term vaginal and caesarean delivery. Cellular localisation of eight prostaglandin pathway proteins was determined by immunohistochemistry.
Expression of prostaglandin pathway genes was differentially affected by factors including gestational age at delivery, and the incidence and duration of labour. Chorioamnionitis/deciduitis was associated with upregulation of PTGS2 (prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)), along with the inflammatory genes IL8 (interleukin 8), S100A8 (S100 calcium binding protein A8) and TLR2 (toll-like receptor 2), in amnion and choriodecidua, and with downregulation of CBR1 (carbonyl reductase 1) and HPGD (hydroxyprostaglandin dehydrogenase 15-(NAD)) in choriodecidua. Protein localisation differed greatly between the various maternal and fetal cell types.
Preterm and term labour are associated with distinct prostaglandin pathway expression profiles; inflammation provokes specific changes, unrelated to the presence of labour; spontaneous and induced term labour are indistinguishable.
Human labour requires a dramatic transition from a state of uterine quiescence and immune tolerance of the fetus—that prevails throughout pregnancy—to a brief period of intense uterine activation involving connective tissue remodelling and coordinated smooth muscle activity. The signals that initiate this process are not yet known, but among the candidates are the prostaglandins, which are known regulators of many aspects of reproductive physiology [1, 2]. Evidence suggests that, during uterine activation there is positive feedback between prostaglandins and inflammatory cytokines that are released by infiltrating leukocytes . Our early studies demonstrated that there is a relationship between inflammatory infiltration of the placenta, fetal membranes and decidua and increased prostaglandin and leukotriene release [4, 5]. Inflammation has been associated with initiation of term and preterm labour both in the presence and absence of observable infection [6–12]. It is therefore possible that prostaglandins and inflammatory pathways are involved in uterine activation. It is important to establish the interactions between these pathways, both for women at risk of preterm birth who may be treated with anti-inflammatory drugs and prostaglandin synthesis inhibitors, and for women facing post-term induction of labour involving prostaglandin treatment.
We have found distinct uterine prostaglandin gene expression and immunolocalisation in the presence of inflammation, suggesting uterine activation occurring through increased PTGS2 expression in the fetal membranes and decreased degradative HPGD in the choriodecidua. Expression patterns in spontaneous preterm and term labour without inflammation differed from each other and from those with inflammatory changes. There were no differences between spontaneous and induced labour at term.
Collection of tissue
Mode of delivery
Number of women
Maternal age (years)
Gestational age at birth (weeks)
Duration of labour (hours)
Emergency: Elective Caesarean section
Membrane rupture (SRM:ARM)
Neonatal gender (male:female)
29 ± 9
33 ± 4
1.7 ± 0.7
27 ± 5
33 ± 1
2.0 ± 0.3
31 ± 3
39 ± 2
4.0 ± 0.4
31 ± 3
40 ± 1
3.6 ± 0.4
32 ± 9
40 ± 2
3.6 ± 0.5
36 ± 7
32 ± 6
2.0 ± 1.3
Quantitative real-time PCR (qPCR)
Primer sequences for quantitative real-time qPCR
Slide-mounted, paraffin-embedded tissue sections were dewaxed in Histoclear (National Diagnostics, Atlanta, GA), hydrated in a graded ethanol series (absolute, 90%, 70% ethanol) and incubated in 1% (w/w) aqueous hydrogen peroxide solution for 15 min to block endogenous peroxidase activity. Antigen retrieval was achieved by incubation in citrate buffer (10 mM sodium citrate, pH6.0, 0.05% (v/v) Tween-20) at 95°C for 20 min. Slides were incubated for 20 min with 2% (v/v) blocking serum, washed with PBS and incubated overnight with primary antibody at the following dilutions: PTGS1 (prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)) 1:60 (sc-1752, Santa Cruz Biotechnology, Santa Cruz, CA); PTGS2 1:60 (sc-1745); AKR1B1 (aldo-keto reductase family 1, member B1 (aldose reductase)) 1:200 (in house, Fortier MA); AKR1C3 (aldo-keto reductase family 1, member C3) 1:200 (ab27491, Abcam, Cambridge, UK); CBR1 1:300 (ab4148); PTGES (prostaglandin E synthase) 1:200 (160140, Cayman Europe, Tallinn, Estonia); HPGD 1:300 (in house, Fortier MA); SLCO2A1 (solute carrier organic anion transporter family, member 2A1) 1:3500 (in house, Fortier MA); VIM (vimentin) 1:200/1:1000 (V4630, Sigma, Gillingham, UK/M7020, DAKO, Ely, UK) in PBS + 3% (w/v) BSA. Slides were washed three times in PBS then incubated for 2 h with biotinylated secondary antibody (Vectastain ABC signal enhancement kit, Vector Labs, Burlingame, CA) diluted 1:200 in PBS + 3% (w/v) BSA. Slides were washed with PBS and incubated for 30 min with Vectastain ABC streptavidin-HRP (horseradish peroxidase) conjugate, washed again and incubated with 3,3’-Diaminobenzidine (DAB, Sigma) for antibody-specific colour development, which was stopped by washing in PBS, before counterstaining nuclei with Mayer’s Haemalum, dehydrating in a graded ethanol series followed by Histoclear and finally coverslip mounting using DPX mountant.
Associations between levels of gene expression and continuous clinical variables (maternal and gestational age, duration of labour) were determined by measuring the probability of significance associated with the Pearson correlation coefficient (using the TDIST function in Excel). Comparisons of expression levels in distinct subgroups of subjects were made in Excel with Student’s t-tests (two-way, not assuming equal variances or equal sample size).
Clinical correlations with PG gene expression
We investigated the possibility of relationships between clinical features of the subjects and prostaglandin gene expression levels in uterine tissues.
Incidence of labour
Gene expression was compared between groups of women matched for gestational age who delivered with or without spontaneous labour. With preterm deliveries, expression was higher with labour for AKR1B1 in choriodecidua and PTGIS in placenta (p = 0.032, 0.028). With term deliveries, expression was higher with labour for PTGES in amnion and AKR1C3 in choriodecidua (p = 0.045, 0.033), while levels of PTGIS, ABCC4 and HPGD in amnion were higher in deliveries without labour (p = 0.043, 0.049, 0.038).
Duration of labour
Duration of labour in spontaneous and induced labour deliveries ranged from 33 minutes to 17 hours. Pearson correlation coefficients were calculated to determine the association between duration of labour and gene expression. Negative correlation, indicating decreasing expression with increasing duration, was seen with expression of CBR1 in amnion (p = 0.006), PTGDS (prostaglandin D2 synthase 21 kDa (brain)), PTGES3 (prostaglandin E synthase 3 (cytosolic)), AKR1C3 and CBR1 in choriodecidua (p = 0.049, 0.011, 0.013, <0.001) and AKR1C3 in placenta (p = 0.031). Positive correlation was seen for PTGES2 (prostaglandin E synthase 2) in amnion (p = 0.022) and SLCO2A1 in choriodecidua (p = 0.010).
Presence of inflammation
Placenta and gestational membranes were collected from women with uterine inflammation, and PG gene expression in this group was compared by t-test with expression in a subgroup of women with no inflammation that was matched for gestational age and mode of delivery (Figure 2). Effects of inflammation were limited to upregulation of PTGS2 in amnion and choriodecidua (p = 0.022, 0.038), and downregulation of CBR1 and HPGD in choriodecidua (p = 0.018, 0.011).
Immunolocalisation of PG pathway proteins in placenta
In the chorionic plate (the surface of the placenta adjacent to the amniotic cavity), the amnion epithelium showed staining for PTGS2 and PTGES (not shown). Extravillous cytotrophoblasts, which form an incomplete layer at the inner border of the chorionic plate, showed staining for HPGD, PTGES, SLCO2A1, AKR1B1, AKR1C3 and CBR1.In the placental villi (Figure 4A-K(i)), syncytiotrophoblasts displayed staining for AKR1B1, HPGD PTGS2, SLCO2A1, CBR1, AKR1C3, and PTGES. Villous fibroblasts showed PTGS2 and SLCO2A1 staining and heterogeneous AKR1B1 staining. Villous macrophages were positive for PTGS1 and PTGES.
Immunolocalisation of PG pathway proteins in uterine cell populations
Immunolocalisation of PG pathway proteins in gestational membranes
The decidual cells showed staining for AKR1B1, HPGD, AKR1C3, PTGS2, SLCO2A1 and CBR1. Chorionic trophoblasts had staining for HPGD, AKR1B1, CBR1, PTGS2, PTGES, AKR1C3 and SLCO2A1. AKR1B1, PTGS2, AKR1C3, HPGD and CBR1 were seen in amniotic and chorionic fibroblasts. PTGS2 and PTGES had immunological reactions in amniotic epithelium. This protein distribution is summarised in Table 3.
Influence of inflammation in fetal membranes on protein localisation
Overlap with previous research
As we have examined multiple members of the prostaglandin pathway in three uterine tissues, there is inevitably a degree of overlap with previous studies of prostaglandin pathway components. For descriptions of the immunolocalisation of prostaglandin pathway proteins, this overlap has been summarised in Table 3, from which it can be seen that we are now presenting novel evidence of uterine immunolocalisation for seven of the eight prostaglandin pathway proteins studied.
Previous descriptions of prostaglandin pathway gene expression have focused largely on the cyclooxygenase/prostaglandin H2 synthase genes PTGS1 and PTGS2 (formerly Cox1 and Cox2). Not all previous observations can be reconciled with each other.
In the placenta, there is evidence suggesting no change in PTGS1 expression with gestational age , and contrasting evidence of decreasing expression with increasing gestational age at labour . In gestational membranes, increasing gestational age has been associated with increased [26, 27], unchanged [27, 28], and decreased PTGS1 expression. Likewise, the incidence of labour has been associated with increased [26, 27] and unchanged [30–36]PTGS1 expression.
In the placenta, the existing evidence suggests that there is no change in expression of PTGS2 with gestational age or clinical chorioamnionitis . In the gestational membranes, several studies have shown higher PTGS2 expression with increasing gestational age [26–29]. There is evidence supporting both increased PTGS2 expression following labour [26–28, 31–35] and no change with labour [20, 36, 37].
Information relating to intrauterine expression of other prostaglandin pathway genes is limited. Our previous work demonstrated expression of the 15 prostaglandin pathway genes in placenta, amnion and choriodecidua . In addition, PLA2G4A (phospholipase A2, group IVA (cytosolic, calcium-dependent)) expression has been identified in human placenta and gestational membranes , as has expression of PTGDS and HPGDS. In placenta and membranes, PTGES expression has shown no change with labour . Expression of AKR1B1, AKR1C3, HPGD and SLCO2A1 has been demonstrated in amnion and choriodecidua . Evidence has been presented in support of unchanged placental expression of HPGD in response to gestational age, labour and intrauterine infection [25, 40], but also in support of increased expression with gestational age . In choriodecidua, there is evidence for lower levels of HPGD mRNA in labour than not-in-labour [24, 37, 40, 42], with further reductions occurring in the presence of intrauterine infection .
The human placenta, fetal membranes and decidua produce prostaglandins throughout pregnancy with a large increase at parturition, but the precise roles of these pleiotropic mediators are yet to be determined. The prostaglandin metabolic pathway consists of anabolic and catabolic components, as well as trans-membrane transporters (Figure 1). We have characterised prostaglandin pathway gene expression and protein localisation in placenta, amnion and choriodecidua from women delivered at different gestational ages with or without labour, induction and intrauterine inflammation. We have described novel protein localisation and gene expression patterns that increase our understanding of the roles of prostaglandins in human pregnancy and labour.
The placenta is the interface between the maternal and fetal blood supplies, allowing nutrient and waste exchange across the thin syncytiotrophoblast layers of numerous highly vascularised fetal villi projecting directly into the placental pool of maternal blood. As the fetal tissues are allogeneic to the maternal tissues, there must be mechanisms at this interface to prevent a maternal immune response to the fetus. We have identified similar patterns of protein localisation in decidual cells and extravillous trophoblasts of the placental bed and syncytiotrophoblasts of placental villi. These cells all express AKR1B1, PTGS2, HPGD, PTGES, SLCO2A1, AKR1C3 and CBR1, thus having the capacity for PGF2 and PGE2 synthesis and PG uptake and degradation. Gene expression patterns described here and in our previous work  support these observations and we now describe the presence of PGD2, PGE2 and PGI2 synthases in the placenta. Comparisons of placental gene expression in different groups of women identified increasing HPGDS, AKR1C3 and ABCC4 with gestational age in the absence of labour, and higher PTGIS in labour than not-in-labour preterm.
The fetal membranes consist of the fetal amnion and chorion and the attached maternal decidua, which together comprise a major structural element of the uterine tissues and have endocrine functions in pregnancy and parturition not yet fully elucidated . As in the placenta, the trophoblast and decidua are the interface between maternal and fetal tissues. Immunolocalisation of prostaglandin pathway proteins in chorionic trophoblast cells and adjacent decidua are similar to each other, and to some extent resemble placental patterns, with HPGD, AKR1B1, AKR1C3, CBR1, PTGS2 and SLCO2A1 expressed in choriodecidua. Unlike in placental cells, variable protein expression is evident in choriodecidua, with the immunolocalisation of PTGES in chorionic trophoblast but not decidua, and higher chorionic levels of CBR1, and decidual levels of AKR1C3. Prostaglandin gene expression changes in choriodecidua include increased AKR1C3 and PTGIS with gestational age and labour, with higher AKR1B1 in labour preterm, and higher AKR1C3 in labour at term compared with not-in-labour.
In the region between the chorionic trophoblast and amniotic epithelium, fibroblasts express PTGS2, PGF2 synthases and HPGD, while the amniotic epithelium itself, which is known to be a source of PGE2 synthesis [43, 44], expresses PTGS2 and PTGES proteins, and also high levels of PTGS2, PTGES and PTGES3 mRNA. Both PTGS2 and PTGES are differentially expressed in amnion, with PTGS2 increasing with gestational age in the presence of labour, and PTGES decreasing as gestational age rises in the absence of labour, and displaying higher expression in labour than not-in-labour at term. Despite previous observations of increased levels of prostaglandins and their metabolites in amniotic fluid with labour [39, 45, 46], we did not observe a significant alteration in PTGS2 in amnion and choriodecidua with either preterm or term labour.
Taken together, these expression patterns suggest distinct roles for prostaglandin metabolism in tissues at the maternal:fetal interface and in tissues within the fetal compartment. At the interface there is the ability to synthesise PGD2, PGE2, and PGF2, but these prostaglandins might be limited to autocrine or paracrine function by the co-expressed degradative complex of SLCO2A1 and HPGD, which is considered to be a barrier between the maternal and fetal prostaglandin systems [24, 47, 48]. These prostaglandins could participate in the immunomodulation of maternal leukocytes present in decidua, placental bed and maternal blood, to prevent rejection of the fetal tissues.
PGE2 synthesised in the amnion and released into the amniotic fluid could influence fetal physiology, for example by inhibiting fetal breathing . The reduction in amniotic PTGES expression and amniotic fluid PGE2 with increasing gestational age might then allow lung movements to develop in sync with fetal maturation. It should, of course, be noted that PTGES is the only one of the three PGE2 synthases that displays this dependence on gestational age for amniotic expression. PTGES is also the only PGE2 synthase that shows higher expression in the amnion than in the other tissues. Furthermore, as amniotic expression of both SLCO2A1 and HPGD are some orders of magnitude lower than in placenta and choriodecidua, it suggests that there is sufficient degradation of the PGE2 that is released into the amniotic cavity in fetal tissues, such as the lung, to prevent accumulation in the amniotic fluid.
In addition to gestational age and the incidence of labour, we investigated the correlation of prostaglandin gene expression with other characteristics. Duration of labour was associated with different expression changes in each of the tissues, with both upregulation and downregulation of prostaglandin genes. The only gene to be affected by both duration of labour and the presence or absence of labour was AKR1C3 in the choriodecidua. This suggests that regulation of some genes is associated with the process of labour, regardless of its duration, whereas others are affected by exposure to the prolonged stressful effects of labour. As we could not follow gene expression throughout labour, we cannot rule out that the differential regulation of these genes is a cause rather than an effect of the duration of labour. In a rarely quoted study involving >200 deliveries, Keski-Nisula et al. demonstrated that decidual inflammation is significantly more common in women in advanced labour compared to early labour, and concluded that the inflammatory changes are more likely to be a consequence of labour rather than its cause . Given the traumatic effects of labour on both mother and child, elucidating the true nature of this relationship could provide valuable information.
We were very interested in evaluating the presence or absence of intrauterine inflammation. There has been a great deal of effort expended on establishing the causative relationship between intrauterine infection, inflammation and labour, particularly preterm labour. The premature activation of inflammatory pathways by intrauterine infection has been proposed as a major contributor to preterm labour [51, 52]. Amniotic fluid metabolomic profiles differ in women delivering preterm in the presence and absence of intra-amniotic infection and inflammation .
We compared gene expression in a group of women with histological signs of inflammation with expression in a group of women matched for gestational age at delivery, and without substantial differences in other recorded variables, but with no signs of inflammation. To confirm the histological observations of inflammation, we measured the expression of three known inflammatory genes, finding significant upregulation of all three in amnion and choriodecidua samples from the INF group. Among the prostaglandin pathway genes, PTGS2 was upregulated with inflammation in both amnion and choriodecidua, whereas CBR1 and HPGD were downregulated in choriodecidua. In the placenta only one of the inflammatory control genes was upregulated, and none of the prostaglandin genes was affected by inflammation, but as the intrauterine inflammation was largely limited to chorioamnionitis/deciduitis, we cannot rule out that placentas affected by villitis, which show altered leukotriene synthesis , would also show prostaglandin pathway expression changes. The unique expression patterns of prostaglandin pathway and inflammatory control genes that we have observed suggest that in cases of uncomplicated spontaneous preterm labour, there is no underlying inflammatory expression profile. There must be an alternative mechanism for uterine activation in SPL in the absence of inflammation. In this regard it is worth mentioning that oxytocin, a strong uterotonic agent, stimulates PTGS2 expression in human myometrial cells through previously undescribed pathways such as NFAT (nuclear factor of activated T cells) .
Although these results support the idea that labour usually occurs in the absence of inflammation, there is evidence that the presence of inflammation can be a trigger for labour, with [8, 12] or without [10, 12] signs of infection. This delivery mechanism can provide a response to intrauterine infections that can threaten the lives of mother and fetus. Tocolysis is not always an appropriate treatment, even for very early preterm labour, as the uterus can become a hostile environment. However, when infections can be overcome, and in instances of premature labour without infection and/or inflammation, there are great potential benefits to effective tocolysis. Our observation of different prostaglandin pathway expression profiles in preterm labour and inflammation could have implications for the choice of tocolytics used in different situations. Although elevation of PTGS2 in placenta and membranes affected by inflammation could be countered by selective PTGS2 inhibitors, PTGS2 is not upregulated with preterm labour in these tissues, although it is in myometrium . Better understanding of the roles of PTGS2 in the different uterine tissues in preterm and term labour with and without inflammation could clarify when PTGS2 inhibitors are most likely to be effective.
We observed an increase in PTGS2 expression in the amnion with term versus preterm labour that has also been seen previously [31, 32, 55]. An increase in amniotic fluid IL1 (interleukin 1) with labour at term has been described , and could be responsible for the PTGS2 upregulation, although as with other observations in this field, there is contradictory evidence suggesting lower IL1 at term . Increased PTGS2 expression induced by cytokines, would explain the upregulation of PTGS2 in the inflamed membranes of chorioamnionitis.
Limitations of this study include the numbers of samples in each of the groups; there is no enough data to correlate with previous preterm deliveries, hypertension, BMI, asthma, smoking and socioeconomic status of the women. Immunohistochemistry was used as a qualitative assay for only a subset of the prostaglandin pathway proteins, so that no quantitative data on protein levels were obtained. Another potential limitation is the lack of statistical correction for multiple comparisons, which could lead to type I errors of false positive identification of statistical significance. However, in order to avoid type II errors of rejection of true significance, we have presented the results of our statistical tests uncorrected, with the caveat that further studies are required before the changes that we have identified can be unequivocally confirmed.
The principal aim of our research is to identify the causes of preterm labour, to enable reliable prediction of its occurrence and to facilitate its prevention by identifying biochemical pathways suitable for intervention. In light of considerable evidence linking prostaglandin function with uterine activation, we have undertaken a detailed analysis of prostaglandin pathway gene expression in human placenta, amnion and choriodecidua, identifying changes in association with gestational age, labour, inflammation and duration of labour, although there were no significant differences between spontaneous and induced labour at term. Inflammation provokes specific changes, unrelated to the presence of labour. The use of tocolytics should take into account these differences, in particular between uncomplicated spontaneous preterm labour and chorioamnionitis. Greater understanding of the different PG pathway changes in idiopathic and inflammation-associated preterm labour should facilitate the targeting of appropriate pharmacological intervention to these very different groups of women.
We are grateful to research midwives Anne Duffner and Alison Kirby for obtaining consent from women at St Michael’s Hospital and organising the collection of samples. Dr Hana Al-Zamil also contributed to sample collection and processing.
This work was supported by Wellbeing of Women [grant RG825].
- Challis JR, Sloboda DM, Alfaidy N, Lye SJ, Gibb W, Patel FA, Whittle WL, Newnham JP: Prostaglandins and mechanisms of preterm birth. Reproduction. 2002, 124: 1-17. 10.1530/rep.0.1240001.View ArticlePubMedGoogle Scholar
- Fortier MA, Krishnaswamy K, Danyod G, Boucher-Kovalik S, Chapdelaine JA: A postgenomic integrated view of prostaglandins in reproduction: implications for other body systems. J Phys Pharm. 2008, 59 (Suppl 1): 65-89.Google Scholar
- Christiaens I, Zaragoza DB, Guilbert L, Robertson SA, Mitchell BF, Olson DM: Inflammatory processes in preterm and term parturition. J Reprod Immunol. 2008, 79: 50-57. 10.1016/j.jri.2008.04.002.View ArticlePubMedGoogle Scholar
- López Bernal A, Hansell DJ, Khong TY, Keeling JW, Turnbull AC: Prostaglandin E production by the fetal membranes in unexplained preterm labour and preterm labour associated with chorioamnionitis. Br J Obstet Gynaecol. 1989, 96: 1133-1139. 10.1111/j.1471-0528.1989.tb03187.x.View ArticlePubMedGoogle Scholar
- López Bernal A, Hansell DJ, Khong TY, Keeling JW, Turnbull AC: Placental leukotriene B4 release in early pregnancy and in term and preterm labour. Early Hum Dev. 1990, 23: 93-99. 10.1016/0378-3782(90)90132-3.View ArticlePubMedGoogle Scholar
- López Bernal A, Hansell DJ, Cañete Soler R, Keeling JW, Turnbull AC: Prostaglandins, chorioamnionitis and preterm labour. Br J Obstet Gynaecol. 1987, 94: 1156-1158. 10.1111/j.1471-0528.1987.tb02315.x.View ArticlePubMedGoogle Scholar
- Mueller-Heubach E, Rubinstein DN, Schwarz SS: Histologic chorioamnionitis and preterm delivery in different patient populations. Obstet Gynecol. 1990, 75: 622-626.PubMedGoogle Scholar
- Hillier SL, Witkin SS, Krohn MA, Watts DH, Kiviat NB, Eschenbach DA: The relationship of amniotic fluid cytokines and preterm delivery, amniotic fluid infection, histologic chorioamnionitis, and chorioamnion infection. Obstet Gynecol. 1993, 81: 941-948.PubMedGoogle Scholar
- Opsjøn SL, Wathen NC, Tingulstad S, Wiedswang G, Sundan A, Waage A, Austgulen R: Tumor necrosis factor, interleukin-1 and interleukin-6 in normal human pregnancy. Am J Obstet Gynecol. 1993, 169: 397-404. 10.1016/0002-9378(93)90096-2.View ArticleGoogle Scholar
- Steinborn A, Günes H, Röddiger S, Halberstadt E: Elevated placental cytokine release, a process associated with preterm labor in the absence of intrauterine infection. Obstet Gynecol. 1996, 88: 534-539. 10.1016/0029-7844(96)00224-4.View ArticlePubMedGoogle Scholar
- Leitich H, Bodner-Adler B, Brunbauer M, Kaider A, Egarter C, Husslein P: Bacterial vaginosis as a risk factor for preterm delivery: a meta-analysis. Am J Obstet Gynecol. 2003, 189: 139-147. 10.1067/mob.2003.339.View ArticlePubMedGoogle Scholar
- Shim SS, Romero R, Hong JS, Park CW, Jun JK, Kim BI, Yoon BH: Clinical significance of intra-amniotic inflammation in patients with preterm premature rupture of membranes. Am J Obstet Gynecol. 2004, 191: 1339-1345. 10.1016/j.ajog.2004.06.085.View ArticlePubMedGoogle Scholar
- Phillips RJ, Al-Zamil H, Hunt LP, Fortier MA, López Bernal A: Genes for prostaglandin synthesis, transport and inactivation are differentially expressed in human uterine tissues, and the prostaglandin F synthase AKR1B1 is induced in myometrial cells by inflammatory cytokines. Mol Hum Reprod. 2011, 17: 1-13. 10.1093/molehr/gaq057.View ArticlePubMedGoogle Scholar
- Xu Y, Knipp GT, Cook TJ: Expression of cyclooxygenase isoforms in developing rat placenta, human term placenta, and BeWo human trophoblast model. Mol Pharm. 2005, 2: 481-490. 10.1021/mp0500519.View ArticlePubMedGoogle Scholar
- Wetzka B, Nüsing R, Charnock-Jones DS, Schäfer W, Zahradnik HP, Smith SK: Cyclooxygenase-1 and -2 in human placenta and placental bed after normal and pre-eclamptic pregnancies. Hum Reprod. 1997, 12: 2313-2320. 10.1093/humrep/12.10.2313.View ArticlePubMedGoogle Scholar
- Meadows JW, Pitzer B, Brockman DE, Myatt L: Differential localization of prostaglandin E synthase isoforms in human placental cell types. Placenta. 2004, 25: 259-265. 10.1016/j.placenta.2003.09.004.View ArticlePubMedGoogle Scholar
- Dunn-Albanese LR, Ackerman WE, Xie Y, Iams JD, Kniss DA: Reciprocal expression of peroxisome proliferator-activated receptor-gamma and cyclooxygenase-2 in human term parturition. Am J Obstet Gynecol. 2004, 190: 809-816. 10.1016/j.ajog.2003.09.052.View ArticlePubMedGoogle Scholar
- Cheung PY, Walton JC, Tai HH, Riley SC, Challis JR: Immunocytochemical distribution and localization of 15-hydroxyprostaglandin dehydrogenase in human fetal membranes, decidua and placenta. Am J Obstet Gynecol. 1990, 163: 1445-1449. 10.1016/0002-9378(90)90603-5.View ArticlePubMedGoogle Scholar
- Breuiller-Fouché M, Leroy MJ, Dubois O, Reinaud P, Chissey A, Qi H, Germain G, Fortier MA, Charpigny G: Differential expression of the enzymatic system controlling synthesis, metabolism, and transport of PGF2 alpha in human fetal membranes. Biol Reprod. 2010, 83: 155-162. 10.1095/biolreprod.109.080390.View ArticlePubMedGoogle Scholar
- Gibb W, Sun M: Localization of prostaglandin H synthase type 2 protein and mRNA in term human fetal membranes and decidua. J Endocrinol. 1996, 150: 497-503. 10.1677/joe.0.1500497.View ArticlePubMedGoogle Scholar
- Alfaidy N, Sun M, Challis JR, Gibb W: Expression of membrane prostaglandin E synthase in human placenta and fetal membranes and effect of labor. Endocrine. 2003, 20: 219-225. 10.1385/ENDO:20:3:219.View ArticlePubMedGoogle Scholar
- Premyslova M, Li W, Alfaidy N, Bocking AD, Campbell K, Gibb W, Challis JR: Differential expression and regulation of microsomal prostaglandin E(2) synthase in human fetal membranes and placenta with infection and in cultured trophoblast cells. J Clin Endocrinol Metab. 2003, 88: 6040-6047. 10.1210/jc.2003-030618.View ArticlePubMedGoogle Scholar
- Meadows JW, Eis AL, Brockman DE, Myatt L: Expression and localization of prostaglandin E synthase isoforms in human fetal membranes in term and preterm labor. J Clin Endocrinol Metab. 2003, 88: 433-439. 10.1210/jc.2002-021061.View ArticlePubMedGoogle Scholar
- Sangha RK, Walton JC, Ensor CM, Tai HH, Challis JR: Immunohistochemical localization, messenger ribonucleic acid abundance, and activity of 15-hydroxyprostaglandin dehydrogenase in placenta and fetal membranes during term and preterm labor. J Clin Endocrinol Metab. 1994, 78: 982-989.PubMedGoogle Scholar
- Hirsch E, Goldstein M, Filipovich Y, Wang H: Placental expression of enzymes regulating prostaglandin synthesis and degradation. Am J Obstet Gynecol. 2005, 192: 1836-1842. 10.1016/j.ajog.2004.12.070.View ArticlePubMedGoogle Scholar
- Mijovic JE, Zakar T, Nairn TK, Olson DM: Prostaglandin endoperoxide H synthase (PGHS) activity and PGHS-1 and -2 messenger ribonucleic acid abundance in human chorion throughout gestation and with preterm labor. J Clin Endocrinol Metab. 1998, 83: 1358-1367.PubMedGoogle Scholar
- Mijovic JE, Zakar T, Angelova J, Olson DM: Prostaglandin endoperoxide H synthase mRNA expression in the human amnion and decidua during pregnancy and in the amnion at preterm labour. Mol Hum Reprod. 1999, 5: 182-187. 10.1093/molehr/5.2.182.View ArticlePubMedGoogle Scholar
- Slater DM, Dennes WJ, Campa JS, Poston L, Bennett PR: Expression of cyclo-oxygenase types-1 and -2 in human myometrium throughout pregnancy. Mol Hum Reprod. 1999, 5: 880-884. 10.1093/molehr/5.9.880.View ArticlePubMedGoogle Scholar
- Johnson RF, Mitchell CM, Giles WB, Bisits A, Zakar T: Mechanisms regulating prostaglandin H2 synthase-2 mRNA level in the amnion and chorion during pregnancy. J Endocrinol. 2006, 188: 603-610. 10.1677/joe.1.06488.View ArticlePubMedGoogle Scholar
- Freed KA, Aitken MA, Brennecke SP, Rice GE: Prostaglandin G/H synthase-1 messenger RNA relative abundance in human amnion, choriodecidua and placenta before, during and after spontaneous-onset labour at term. Gynecol Obstet Invest. 1995, 39: 73-78. 10.1159/000292383.View ArticlePubMedGoogle Scholar
- Hirst JJ, Teixeira FJ, Zakar T, Olson DM: Prostaglandin endoperoxide-H synthase-1 and -2 messenger ribonucleic acid levels in human amnion with spontaneous labor onset. J Clin Endocrinol Metab. 1995, 80: 517-523.PubMedGoogle Scholar
- Slater DM, Berger LC, Newton R, Moore GE, Bennett PR: Expression of cyclooxygenase types 1 and 2 in human fetal membranes at term. Am J Obstet Gynecol. 1995, 172: 77-82. 10.1016/0002-9378(95)90087-X.View ArticlePubMedGoogle Scholar
- Slater D, Allport V, Bennett P: Changes in the expression of the type-2 but not the type-1 cyclo-oxygenase enzyme in chorion-decidua with the onset of labour. Br J Obstet Gynaecol. 1998, 105: 745-748. 10.1111/j.1471-0528.1998.tb10205.x.View ArticlePubMedGoogle Scholar
- Zakar T, Olson DM, Teixeira FJ, Hirst JJ: Regulation of prostaglandin endoperoxide H2 synthase in term human gestational tissues. Acta Physiol Hung. 1996, 84: 109-118.PubMedGoogle Scholar
- Mijovic JE, Zakar T, Nairn TK, Olso DM: Prostaglandin-endoperoxide H synthase-2 expression and activity increases with term labor in human chorion. Am J Physiol. 1997, 272: E832-840.PubMedGoogle Scholar
- Hirst JJ, Mijovic JE, Zakar T, Olson DM: Prostaglandin endoperoxide H synthase-1 and -2 mRNA levels and enzyme activity in human decidua at term labor. J Soc Gynecol Investig. 1998, 5: 13-20. 10.1016/S1071-5576(97)00101-9.View ArticlePubMedGoogle Scholar
- Makino S, Zaragoza DB, Mitchell BF, Yonemoto H, Olson DM: Decidual activation: abundance and localization of prostaglandin F2alpha receptor (FP) mRNA and protein and uterine activation proteins in human decidua at preterm birth and term birth. Placenta. 2007, 28: 557-565. 10.1016/j.placenta.2006.06.010.View ArticlePubMedGoogle Scholar
- Freed KA, Moses EK, Brennecke SP, Rice GE: Differential expression of type II, IV and cytosolic PLA2 messenger RNA in human intrauterine tissues at term. Mol Hum Reprod. 1997, 3: 493-499. 10.1093/molehr/3.6.493.View ArticlePubMedGoogle Scholar
- Helliwell RJ, Keelan JA, Marvin KW, Adams L, Chang MC, Anand A, Sato TA, O’Carroll S, Chaiworapongsa T, Romero RJ, Mitchell MD: Gestational age-dependent up-regulation of prostaglandin D synthase (PGDS) and production of PGDS-derived antiinflammatory prostaglandins in human placenta. J Clin Endocrinol Metab. 2006, 91: 597-606. 10.1210/jc.2005-1982.View ArticlePubMedGoogle Scholar
- van Meir CA, Matthews SG, Keirse MJ, Ramirez MM, Bocking A, Challis JR: 15-hydroxyprostaglandin dehydrogenase: implications in preterm labor with and without ascending infection. J Clin Endocrinal Metab. 1997, 82: 969-976.Google Scholar
- Schoof E, Girstl M, Frobenius W, Kirschbaum M, Repp R, Knerr I, Rascher W, Dötsch J: Course of placental 11beta-hydroxysteroid dehydrogenase type 2 and 15-hydroxyprostaglandin dehydrogenase mRNA expression during human gestation. Eur J Endocrinol. 2001, 145: 187-192. 10.1530/eje.0.1450187.View ArticlePubMedGoogle Scholar
- Pomini F, Patel FA, Mancuso S, Challis JR: Activity and expression of 15-hydroxyprostaglandin dehydrogenase in cultured chorionic trophoblast and villous trophoblast cells and in chorionic explants at term with and without spontaneous labor. Am J Obstet Gynecol. 2000, 182: 221-226. 10.1016/S0002-9378(00)70516-3.View ArticlePubMedGoogle Scholar
- Myatt L, Sun K: Role of fetal membranes in signaling of fetal maturation and parturition. Int J Dev Biol. 2010, 54: 545-553. 10.1387/ijdb.082771lm.View ArticlePubMedGoogle Scholar
- López Bernal A, Newman GE, Phizackerley PJR, Turnbull AC: Surfactant stimulates prostaglandin E production in human amnion. Br J Obstet Gynaecol. 1988, 95: 1013-1017. 10.1111/j.1471-0528.1988.tb06506.x.View ArticlePubMedGoogle Scholar
- Mitchell MD, Keirse MJ, Brunt JD, Anderson AB, Turnbull AC: Concentrations of the prostacyclin metabolite, 6-keto-prostaglandin F1 alpha, in amniotic fluid during late pregnancy and labour. Br J Obstet Gynaecol. 1979, 86: 350-353. 10.1111/j.1471-0528.1979.tb10609.x.View ArticlePubMedGoogle Scholar
- Lee SE, Romero R, Park IS, Seong HS, Park CW, Yoon BH: Amniotic fluid prostaglandin concentrations increase before the onset of spontaneous labor at term. J Matern Fetal Neonatal Med. 2008, 21: 89-94. 10.1080/14767050701830514.View ArticlePubMedGoogle Scholar
- Keirse MJ, Turnbull AC: Metabolism of prostaglandins within the pregnant uterus. Br J Obstet Gynaecol. 1975, 82: 887-893. 10.1111/j.1471-0528.1975.tb00593.x.View ArticlePubMedGoogle Scholar
- Nomura T, Lu R, Pucci ML, Schuster VL: The two-step model of prostaglandin signal termination: in vitro reconstitution with the prostaglandin transporter and prostaglandin 15 dehydrogenase. Mol Pharmacol. 2004, 65: 973-978. 10.1124/mol.65.4.973.View ArticlePubMedGoogle Scholar
- Sorokin Y, Hallak M, Klein O, Kalderon I, Abramovici H: Effects of induction of labor with prostaglandin E2 on fetal breathing and body movements: controlled, randomized, double-blind study. Obstet Gynecol. 1992, 80: 788-791.PubMedGoogle Scholar
- Keski-Nisula L, Aalto ML, Katila ML, Kirkinen P: Intrauterine inflammation at term: a histopathologic study. Hum Pathol. 2000, 31: 841-846. 10.1053/hupa.2000.8449.View ArticlePubMedGoogle Scholar
- Goldenberg RL, Hauth JC, Andrews WW: Intrauterine infection and preterm delivery. N Engl J Med. 2000, 342: 1500-1507. 10.1056/NEJM200005183422007.View ArticlePubMedGoogle Scholar
- Romero R, Espinoza J, Kusanovic JP, Gotsch F, Hassan S, Erez O, Chaiworapongsa T, Mazor M: The preterm parturition syndrome. Br J Obstet Gynaecol. 2006, 113 (Suppl 3): 17-42.View ArticleGoogle Scholar
- Romero R, Mazaki-Tovi S, Vaisbuch E, Kusanovic JP, Chaiworapongsa T, Gomez R, Nien JK, Yoon BH, Mazor M, Luo J, Banks D, Ryals J, Beecher C: Metabolomics in premature labor: a novel approach to identify patients at risk for preterm delivery. J Matern Fetal Neonatal Med. 2010, 23: 1344-1359. 10.3109/14767058.2010.482618.View ArticlePubMedPubMed CentralGoogle Scholar
- Pont JN, McArdle CA, López Bernal A: Oxytocin-stimulated NFAT transcriptional activation in human myometrial cells. Mol Endocrinol. 2012, 26: 1743-1756. 10.1210/me.2012-1057.View ArticlePubMedPubMed CentralGoogle Scholar
- Fuentes A, Spaziani EP, O’Brien WF: The expression of cyclooxygenase-2 (COX-2) in amnion and decidua following spontaneous labor. Prostaglandins. 1996, 52: 261-267.View ArticlePubMedGoogle Scholar
- Romero R, Parvizi ST, Oyarzun E, Mazor M, Wu YK, Avila C, Athanassiadis AP, Mitchell MD: Amniotic fluid interleukin-1 in spontaneous labor at term. J Reprod Med. 1990, 35: 235-238.PubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2393/14/241/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.