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PPAR Research
Volume 2008 (2008), Article ID 758562, 9 pages
Review Article

Placental Implications of Peroxisome Proliferator-Activated Receptors in Gestation and Parturition

1Université d'Auvergne, JE 2447, ARDEMO, Clermont-Ferrand 63000, France
2INSERM, U.384, Laboratoire de Biochimie, Faculté de Médecine, Clermont-Ferrand 63000, France
3CHU Clermont-Ferrand, Maternité, Hôtel-Dieu, Clermont-Ferrand 63000, France

Received 4 June 2007; Revised 13 August 2007; Accepted 26 October 2007

Academic Editor: Pascal Froment

Copyright © 2008 Valerie Borel 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.


The placenta is a transitory structure indispensable for the proper development of the embryo and fetus during mammalian gestation. Like other members of the nuclear receptor family, the peroxisome proliferator-activated receptors (PPARs) are known to be involved in the physiological and pathological events occurring during the placentation. This placental involvement has been recently reviewed focusing on the early stages of placental development (implantation and invasion, etc.), mouse PPARs knockout phenotypes, and cytotrophoblast physiology. In this review, we describe the placental involvement of PPARs (e.g., fat transport and metabolism, etc.) during the late stages of gestation and in the amniotic membranes, highlighting their roles in the inflammation process (e.g., chorioamnionitis), metabolic disorders (e.g., diabetes), and parturition.

1. The Peroxisome Proliferator-Activated Receptors (PPARs)

1.1. Nomenclature and Structure

Discovered in 1990, PPARs are known for their biological role in inducing the proliferation of peroxisomes in rodents [1]. They are transcription factors belonging to the ligand-activated nuclear hormone receptor superfamily [2] and have been identified in different species such as the xenopus, mouse, rat, and humans. In all these species, PPARs present three isotypes encoded by distinct single-copy genes: PPARα (NR1C1), PPARβ/δ (also called NUC1 or NR1C2), and PPARγ (NR1C3), located on chromosomes 15, 17, 6 in the mouse and chromosomes 22, 6, 3 in humans, respectively. The PPARγ gene alternative promoters give rise to three different isoforms named γ1, γ2, and γ3 which differ at their ends (see Figure 1(a)) [3]. PPAR α, β, γ1/γ3, γ2 translation produces proteins of 468, 441, 475, and 505 amino acids, respectively, with a molecular weight of 49 to 56 kDa [4]. By performing multiple PPAR nucleotide/protein alignments of PPARs in different species, a strong interspecies identity (human, mouse, rat, bovine, 90%) has been established, illustrating a strong evolutionary conservation among species by derivation from a common ancestor (Table 1). PPARγ shows the highest conservation in terms of cDNA and proteins.

Table 1: Percentage of nucleotide and amino acid identity between the human, mouse, rat, and bovine PPAR sequences. No PPARγ3 alignment was carried out owing to lack of data on different species. The different sequences came from Ensembl and were aligned with Genomatix software.
Figure 1: (a) Schematic representation of PPARγ genes, mRNA, and proteins. The exons A1, A2, B can be alternatively spliced to give rise to the different PPARγ isoforms. The boxes 1 to 6 correspond to exons which are common to PPARγ1, γ2, γ3 genes. ATG is the initiation transcription site. The molecular weight of these isoforms ranges from 49 to 56 kDa. (b) Schematic representation of typical nuclear receptor structure. AF1: activating function 1 (ligand-independent function), AF2: activating function 2 (ligand-dependent function), NLS: nuclear signal localization.

Like several other members of the nuclear receptor superfamily, PPARs possess the typical structure organised in six domains named A to F (see Figure 1(b)) [5]. Domain C (DBD: DNA binding domain) contains two zinc fingers and allows promoter target gene interaction and dimerization with its preferential nuclear receptor: retinoid X receptor (RXR). The PPAR/RXR heterodimer binds to the target gene promoter response element named peroxisome proliferator response element (PPRE) which is made up of two half site AGGTCA separated by one or two nucleotides (also called DR1 or DR2 for direct repeat 1 or 2) and a extension A (A/T) CT. Domain E/F allows ligand binding and contains a ligand-dependent transactivation function called AF2 (activating function 2). It is involved in dimerization and interaction with cofactors.

1.2. PPAR Ligands

As with the other nuclear receptors, the binding of the ligand is a key step in the control of PPAR transcriptional activity. In the absence of a ligand, corepressors and histone deacetylases (HDAC) bind to PPARs and inhibit the transcription activation of target genes. PPAR ligands have the ability to dissociate the corepressor complexes from the PPAR/RXR heterodimer, allowing the binding of the coactivators in order to initiate and activate transcription.

There are two kinds of ligands for the PPARs: natural and synthetic. Among the natural ligands the monounsaturated fatty acids (FA) (e.g., oleic acid) and the polyunsaturated fatty acids (PUFA) (e.g., linoleic acid, linolenic acid, and arachidonic acid) are described as ligands for PPARα, PPARβ, and PPARγ. They act with concentrations consistent with those found in human serum [6]. The different PUFA metabolites: 8(S)- and 15-hydroxyeicosatetraenoic acid (8(S)- and 15-HETE), leukotriene B4 (LTB4), 9- and 13-hydroxyoctadedienoic acid (9-HODE and 13-HODE) and 15-deoxy-Δ12, 14-prostaglandin J2 (PGJ2) are potent selective activators of PPARα and PPARγ. Some oxidized low-density lipoproteins (LDLs), oxidized alkyphospholipids, nitrolinolenic acid, and prostaglandin metabolites can also activate PPARγ [7]. Recently, it has been demonstrated that P450 eicosanoids are potent PPARα and PPARγ ligands [8]. Indeed, Ng et al. [8] have shown that P450 catalysed arachidonic acid metabolites like 20-hydroxyeicosatetraenoic acid (20-HETE) or 11, 12-epoxyeicosatrienoic acid (11, 12-EET) can activate PPARα and PPARγ. These ligands induce PPAR binding to PPRE and can modify the expression of PPARα responsive genes like apoA-I or apoA-II in the same way than synthetic ligands. Thus the finely regulated conversion of PUFAs to eicosanoids through either the lipoxygenase, cyclooxygenase, or cytochrome P450 monooxygenase pathways may provide a mechanism for the differential regulation of PPARα and PPARγ and their respective target genes. PPARβ can be activated by different types of eicosanoids including prostaglandinA1 (PGA1) and prostaglandin D2 (PGD2). Many synthetic ligands exist and have been used in PPAR work. These ligands include prostaglandin 12 analogs, pirinixic acid (Wy-14643) for PPARα, hypolipidemic and hypoglycemic agents (nonthiazolidinedione) for PPARβ, and thiazolidinediones (e.g., rosiglitasone, troglitazone) for PPARγ [2].

2. PPAR Expression Patterns

The adult PPAR expression patterns have been extensively established at the mRNA and protein levels in several species (Table 2) [8, 9]. Several studies conducted during mammalian gestation have established the placenta as an important expression site of the different PPARs isoforms. Our review will focus only on term placental expression and on the amniotic/fetal membranes. The placental dynamic expression of the 3 PPARs during early and midgestation (of mouse, rat, and human) is well described in Fournier et al., 2007 [4]. In rat placenta, all three PPAR isoforms are ubiquitously expressed from 11 days postcoitum (dpc) [10]. Both PPARβ/δ and PPARγ are expressed after 8.5 dpc in mouse placenta. By immunohistochemistry and RT-PCR, the three PPAR isoforms are been shown to be expressed in the villous trophoblastic cells and syncytiotrophoblasts of the human term placenta [4]. To extend the previously published results [11] and to assess the potential importance of PPAR proteins in fetal membranes, RT-PCR and immunohistochemistry experiments were performed on human term placental samples. The three PPARs are present in total placenta, amnion, chorion, and in amnion-derived WISH epithelial cell line at the mRNA (see Figure 2(a)) and protein levels (see Figure 2(b)). The expression of PPARα and PPARγ seems to be weaker than that observed for PPARβ/δ. In addition, a greater amplification of the PPARγ cDNA is obtained in chorion than in amnion, where PPARγ is almost undetectable.

Table 2: Summary of PPAR expression patterns.
Figure 2: PPARs expression in term placenta and amniotic membrances. (a) RT-PCR assays of PPARα, PPARβ, and PPARγ mRNA in amnion, chorion, placenta, and WISH cells. PCR products were analyzed on 1.8% agarose gel and stained with ethidium bromide. 36B4 corresponds to the housekeeping gene. A: Amnion, C: Chorion, A+C: Amnino+Chorion, P: Total placenta, W: WISH cells. (b) PPARs immunostaining of amnion and chorion. Note that all PPARs are expressed in nucleus. Magnification: x200.

3. Implications of PPARs in Placenta and Fetal Membranes

3.1. Placental and Amniotic Presence of PPARs Ligands

The lipids of human amnion and chorion are enriched in the essential fatty acid arachidonic acid, which is the precursor of all the prostaglandins of the 2 series [13]. Sixty-six percent of the arachidonic acid of the human fetal membranes are available in the glycerophospholipids of these tissues and can easily be converted into PGD2 [14]. The placenta produces considerable amounts of PGD2 [15]. The enzymes necessary to convert PGD2 into prostaglandin J2 (PGJ2) are present and coexpressed with PPARγ in placenta. 15-Deoxy-Δ12, 14-PGJ2 (15dPGJ2) and its precursor PGD2 are present in amniotic fluid at concentrations that do not exceed 3 nM [16]. However, this amniotic fluid concentration cannot be an exact representation of the physiological placental reality for PPARs ligands because the nuclear concentration is not measured. The maternal blood may also be a source of PPAR ligands for the human placenta and the fetal membranes. It has been established that a heat-stable compound (not a protein, but rather a prostanoid or a fatty acid) is detected in maternal blood serum and is able to activate the PPARγ [17]. The presence of classical and new PPARs ligands (e.g., P450 eicosanoids, PUFA metabolites) in placenta and fetal membranes suggests that they could activate PPAR, induce PPAR binding to PPRE, and modify the expression of PPAR target genes; but this hypothesis has to be confirmed by further analysis, based on PPARs activation in other organs. For example, PUFAs, such as and eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), increased PPARγ mRNA expression and binding to PPRE in renal tubular epithelial cell line (HK-2). Furthermore, they downregulate LPS-induced activation of NF-κB via a PPARγ-dependent pathway in HK-2 cells [18]. Another example showed that PGD2 is among the most abundantly produced prostaglandins in synovial fluid by synovial fibroblasts [19]. It can be converted into PGJ2. It has been demonstrated that PPARγ ligands (15dPGJ2) inhibit IL-1β–induced production of nitric oxide (NO) and matrix metalloproteinase-13 (MMP-13) in chondrocytes. This inhibition was PPARγ-dependent and occurred at the transcriptional level, through repression of NF-κB signalling [20]. These two examples support a role of PPAR ligands in fetal membranes.

3.2. Fundamental Implications of PPARs during Early Placentation

As a determining result, the knockout of the PPARγ in mice [21] yielded the first findings indicating the importance of this factor in early embryonic and perinatal development. These results are concomitant with those obtained by the generation of RXRα or β null mice (PPARγ partner in the functional heterodimer), also showing an embryonic lethality explained by the lack of generation of a functional labyrinthine zone [22]. Furthermore, complementary studies conducted by the inactivation of PPARγ coactivators or coregulators, such as peroxisome proliferators activator receptor-binding protein (PBP) and peroxisome proliferator-activated receptor-interacting protein (PRIP), also lead to severe placental dysfunction, such as inadequate vascularisation of the structure [2325]. Recently, Barak et al. also demonstrated that the inactivation of PPARβ/δ led to the formation of abnormal gaps and a thinner but fully differentiated vascular structure in the placentodecidual interface [26]. These results establish the nonredundant roles of PPARγ and PPARβ/δ in early mouse placental development. By contrast, the inactivation of PPARα has no effect on placental formation or on the developing foetus and by the way theirs possible roles during pregnancy had to be clarified [2]. In humans, the studies are almost exclusively focused on the PPARγ roles during early placentation. It has been clearly established that all three PPARs can stimulate or inhibit the differentiation and/or proliferation of the villous cytotrophoblasts into syncytiotrophoblasts and the synthesis of chorionic gonadotrophic hormone, and may hamper extravillous trophoblastic cell invasion (for more details, see Fournier et al., 2007 [4]).

3.3. Roles of PPARs in the Uptake and Transport of Trophoblastic Lipids

As one of the first functions described for PPARγ in other tissues, trophoblastic lipid uptake and accumulation are also regulated in part by this factor [27]. The PPARγ ligands seem to increase the uptake and accumulation of the fatty acids in human placenta [28]. This regulation is associated with an enhanced expression of adipophilin (fat droplet-associated protein) and fatty acid transport proteins (1 and 4) in human trophoblasts [2830]. These results were confirmed recently by the in vivo activation of PPARγ by its agonist rosiglitazone in mice, which also leads to the enhancement of the previous described genes plus two new ones involved in the lipid transport: S3-12 (plasma associated protein) and myocardial lipid droplet protein/MLDP [27]. Taken together, these results confirm the results obtained on PPARγ-null mutants: the absence of the lipid droplets normally present around the fetal vessels in the wild-type placenta [21].

3.4. PPARs in Placental Inflammatory Response and in the Parturition Signalling

At this stage of our knowledge of PPARs, the most interesting results have been obtained with the study of their involvement in the inflammation process, which may be linked to labor at term and also to the premature rupture of fetal membranes (see Figure 3). Term labor is associated with an increase in proinflammatory proteins and cytokines such as IL1β, IL6, IL8, IL10, and TNF-α. This increase in proinflammatory proteins and cytokines induces uterine contractions. PPARγ ligands have been demonstrated to inhibit the secretion of IL6, IL8, and TNF-α in amnion and chorion [31], highlighting the role of PPARs in the regulation of the inflammatory response in human gestational tissues and cells [3235]. The parathyroid hormone-related protein (presenting a cytokine-like action) is involved in many processes during normal and pathological pregnancies, and is decreased by PPARγ stimulation [36], which also blocks proinflammatory cytokine release by adiponectin and leptin [37]. The production of prostaglandins by the endometrium, the myometrium, and the fetal membranes induces the contraction of the myometrium during labor. This generation of uterotonic prostaglandins correlates with the increased prostaglandin-endoperoxide synthase type 2/cyclooxygenase type 2 (COX-2) activity and the increased secretory phospholipase A2-IIA (sPLA2) mRNA, proteins and activities. By inhibiting the production of the COX-2 and sPLA2 in fetal membranes, PPARγ promotes the quiescence of the uterus during gestation [34]. The molecular action of 15dPGJ2 seems to involve interactions of the NF-Kappa B signaling pathway, inducing reduction of PGF2α, PGE2, and MMP9 release in the placental environment [31]. This suppressive action of PPARγ on inflammation is aPPARently time-dependent during pregnancy. The PPARγ level of expression remains stable throughout gestation, except for the period just before labor, when its expression in fetal membranes declines. This reduction is coincidental with a relative increase in COX-2 expression [38]. Further work has shown this simple scheme to be more complex. While the expression of PPARα does not change at term in amnion, it decreases in chorion. An increase was also demonstrated for PPARβ/δ in chorionic and amniotic zones [11]. These last two findings raise the question of the involvement of the α and β isoforms in this process. The absence of a real link between COX-2 and PPARγ is presented by Lindstrom and Bennett [39]. Finally, the PPAR action seems to be concentration-dependent. A small amount of 15dPGJ2 (<0.1  M) acts through the PPARγ signaling pathway, where at high concentration (1  M) its actions are most probably mediated through other pathways: PPARβ/δ and/or an inhibition of NF-κB independent of PPARs [35]. Furthermore, 15dPGJ2 and troglitazone were also demonstrated to have some antiinflammatory or apoptosis-induction specific effects by PPARγ-independent pathways. This was suggested by the work of Lappas et al. on human gestational tissues, demonstrating that this effect could passed by antagonist effect of 15dPGJ2 on the NF-κB pathways and antioxidant effects of the troglitazone, a synthetic ligand of PPARγ [31].

Figure 3: Schematic representation of PPARγ implication in pregnancy maintenance and labor. IL1β: Interleukin 1β; IL6: Interleukin 6; IL8: Interleukin 8; IL10: Interleukin 10, TNFα: Tumor Necrosis Factor α; COX2: Cyclo-oxygenase type 2; PLA2: Phospholipase A2; NF-κB: Nuclear Factor-Kappa B; MMP9: Matrix Metalloproteinase 9; 15dPGJ2: 15-Deoxy-Δ12, 14-prostaglandin J2.
3.5. PPARs in Placental and Amniotic Membranes Pathologies

In contrast to the different roles described for PPARs during human placentation, only a few studies on PPARs and placental pathologies have been conducted. In choriocarcinoma and hydatiform moles, a downregulation of the PPARγ expression is observed but this real influence needs to be elucidated [40]. The potential involvement of PPARγ on preeclampsia is suggested by the fact that this pathology is associated with an increased peroxidation in trophoblasts [41, 42]. An overproduction of 15-HETE has also been noted, suggesting a deregulation of PPARγ [43]. This can cause a strong transactivation of PPARγ during early pregnancy, resulting in a reduction of extravillous trophoblastic invasion, one cellular explanation often cited in the physiopathology of preeclampsia [44, 45]. Other abnormal transactivation of PPARs may be hypothesized to explain placental pathologies. The 15dPGJ2 has been shown to induce apoptosis of the placental (JEG-3) and amniotic (WISH) established cell line, [46, 47]. An excess of 15dPGJ2 production can be a source of placental dysfunction linked to an increase in trophoblastic death. It is also established that deletion of PPARγ, PPARβ/δ, and some of their coactivators (PBP, PRIP, and RAP250) induce abnormal placental phenotypes (abruption, reduction of fetomaternal exchanges, and alterations of trophoblastic differentiation) in null mutants [21, 23, 24, 26, 48, 49]. Chromosomal and/or genetic alterations (point mutation or deletion) may occur for these genes, inducing human placental alterations. The placental 11 hydroxysteroid dehydrogenase type 2 is a target gene of PPARs [50]. This enzyme plays a key role in fetal development by controlling fetal exposure to maternal glucocorticoids. An abnormal regulation by PPARs may result in an absence of fetal protection. In the rat placental HRP-1 established cell line, the phthalate and derivatives transactivate PPARs (α and γ) induced an increase in uptake rates of fetal essential fatty acid and the transport of arachidonic and docosahexaenoic acid [51]. If such a mechanism can be induced by the phthalates during human placentation, this may strongly affect the fetal essential fatty acid content during growth.

Gestational diabetes is linked to impaired lipids metabolism [52]. Decreased 15dPGJ2 in blood of diabetic mothers is also linked to a decrease in placental PPARγ expression. The inhibition of PPARγ results in an induction of a placental proinflammatory environment associated with an increase in nitrogen monoxide production and release, which can impair fetoplacental development [53, 54].

The PPAR regulation of inflammation may be very important in another obstetrical pathology of the amniotic membranes: the chorioamnionitis. This pathology, usually due to an ascendant colonization of pathogenic microorganisms from the vagina to the uterus, is closely associated with preterm labor and premature rupture of membranes (chorion and amnion). These ruptures of membranes seem to arise from deregulated proinflammatory factor synthesis. It has already been reported in this pathology that IL1β, IL6, IL8, TNF-α, and prostaglandinE(2) show inadequate concentrations in placental membrane and in amniotic fluid [5558]. As PPARs may be involved in the occurrence and control of this inflammatory response, further studies are needed to assess their importance in this process and to find new possible therapeutic strategies to prevent this damaging pathology.

More generally, the use of natural and synthetic PPAR ligands looks to be a promising way in preventing placental pathologies such as endometriosis or preeclampsia. An interesting study also demonstrates that the reduction of LPS induction of cytokines is reduced by PPARγ ligands in fetal membranes. Nevertheless, the few studies already conducted were done practically only on animal (rodent) models and looks to have positive effects on the pathologies (for review see Toth et al. [59]). Till now, the major problem using, for example, TZD (thiazolidinedionzes) linking to the PPARγ pathways still the numerous adverse effects of this kind of treatment (e.g., weight gain, anemia, leukopenia, etc.). These facts and the potential placental impacts raised also the question of the use of these medical drugs to treat the gestational diabetes. Perhaps, at the level of clinician actual knowledge, PPARγ and its ligands could be used in a first time, only as good early marker candidates for the diagnosis of pregnancy pathologies like, for example, preeclampsia.

4. Conclusion

Since the discovery of the PPARs, there has been a marked increase in available data on their involvement in mammalian development. Concerning the placenta, all PPARs, but particularly PPARγ, are essential for multiple physiological functions of the trophoblastic and amniotic parts, leading to major involvement of PPARs in the pathophysiology of gestational diseases. However, special care must be taken when this particular PPAR signaling cascade is involved, because part of the regulation may involve PPAR ligand signalling (by the natural 15dPGJ2 ligand or the troglitazone synthetic ligand) but may be transduced by independent nuclear receptor pathways (as, e.g., by antagonizing effects on NF-κB pathway for 15dPGJ2 and by acting as an antioxidant for troglitazone). This last point introduces a new level of complexity in PPAR biology. It does not close preclusion of the eventual use of PPARs for therapeutic treatment during pregnancy, but future medical applications seem still to be a long way off. We can reasonably expect to see some obstetrical use of PPARs in diagnosis (detection of PPARs mutations in intrauterine growth retardation, predisposition of preeclampsia) and therapeutics (tocolysis or treatment of chorioamniotis).


  1. W. T. Schaiff, Y. Barak, and Y. Sadovsky, “The pleiotropic function of PPAR γ in the placenta,” Molecular and Cellular Endocrinology, vol. 249, no. 1-2, pp. 10–15, 2006. View at Publisher · View at Google Scholar · View at PubMed
  2. P. Froment, F. Gizard, D. Defever, B. Staels, J. Dupont, and P. Monget, “Peroxisome proliferator-activated receptors in reproductive tissues: from gametogenesis to parturition,” Journal of Endocrinology, vol. 189, no. 2, pp. 199–209, 2006. View at Publisher · View at Google Scholar · View at PubMed
  3. T. Fournier, V. Tsatsaris, K. Handschuh, and D. Evain-Brion, “PPARs and the placenta,” Placenta, vol. 28, no. 2-3, pp. 65–76, 2007. View at Publisher · View at Google Scholar · View at PubMed
  4. I. Issemann and S. Green, “Activation of a member of the steroid hormone receptor superfamily by peroxisome proliferators,” Nature, vol. 347, no. 6294, pp. 645–650, 1990. View at Publisher · View at Google Scholar · View at PubMed
  5. L. Michalik, B. Desvergne, C. Dreyer, M. Gavillet, R. N. Laurini, and W. Wahli, “PPAR expression and function during vertebrate development,” International Journal of Developmental Biology, vol. 46, no. 1, pp. 105–114, 2002.
  6. L. Fajas, D. Auboeuf, and E. Raspe et al., “The organization, promoter analysis, and expression of the human PPARγ gene,” The Journal of Biological Chemistry, vol. 272, no. 30, pp. 18779–18789, 1997. View at Publisher · View at Google Scholar
  7. P. Escher and W. Wahli, “Peroxisome proliferator-activated receptors: insight into multiple cellular functions,” Mutation Research, vol. 448, no. 2, pp. 121–138, 2000. View at Publisher · View at Google Scholar
  8. B. Desvergne and W. Wahli, “Peroxisome proliferator-activated receptors: nuclear control of metabolism,” Endocrine Reviews, vol. 20, no. 5, pp. 649–688, 1999. View at Publisher · View at Google Scholar
  9. V. Y. Ng, Y. Huang, L. M. Reddy, J. R. Falck, E. T. Lin, and D. L. Kroetz, “Cytochrome P450 eicosanoids are activators of peroxisome proliferator-activated receptor α,” Drug Metabolism and Disposition, vol. 35, no. 7, pp. 1126–1134, 2007. View at Publisher · View at Google Scholar · View at PubMed
  10. P. Escher, O. Braissant, S. Basu-Modak, L. Michalik, W. Wahli, and B. Desvergne, “Rat PPARs: quantitative analysis in adult rat tissues and regulation in fasting and refeeding,” Endocrinology, vol. 142, no. 10, pp. 4195–4202, 2001. View at Publisher · View at Google Scholar
  11. Q. Wang, H. Fujii, and G. T. Knipp, “Expression of PPAR and RXR isoforms in the developing rat and human term placentas,” Placenta, vol. 23, no. 8-9, pp. 661–671, 2002. View at Publisher · View at Google Scholar
  12. E. B. E. Berry, R. Eykholt, R. J. A. Helliwell, R. S. Gilmour, M. D. Mitchell, and K. W. Marvin, “Peroxisome proliferator-activated receptor isoform expression changes in human gestational tissues with labor at term,” Molecular Pharmacology, vol. 64, no. 6, pp. 1586–1590, 2003. View at Publisher · View at Google Scholar · View at PubMed
  13. B. E. Schwarz, F. M. Schultz, P. C. Macdonald, and J. M. Johnston, “Initiation of human parturition. III. fetal membrane content of prostaglandin E2 and F2α precursor,” Obstetrics and Gynecology, vol. 46, no. 5, pp. 564–568, 1975.
  14. J. R. Okita, P. C. MacDonald, and J. M. Johnston, “Mobilization of arachidonic acid from specific glycerophospholipids of human fetal membranes during early labor,” Journal of Biological Chemistry, vol. 257, no. 23, pp. 14029–14034, 1982.
  15. M. D. Mitchell, D. L. Kraemer, and D. M. Strickland, “The human placenta: a major source of prostaglandin D2,” Prostaglandins Leukotrienes and Medicine, vol. 8, no. 4, pp. 383–387, 1982. View at Publisher · View at Google Scholar
  16. R. J. Helliwell, J. A. Keelan, and K. W. Marvin et al., “Gestational age-dependent up-regulation of prostaglandin D synthase (PGDS) and production of PGDS-derived antiinflammatory prostaglandins in human placenta,” Journal of Clinical Endocrinology & Metabolism, vol. 91, no. 2, pp. 597–606, 2006. View at Publisher · View at Google Scholar · View at PubMed
  17. L. L. Waite, E. C. Person, Y. Zhou, K. H. Lim, T. S. Scanlan, and R. N. Taylor, “Placental peroxisome proliferator-activated receptor-γ is up-regulated by pregnancy serum,” Journal of Clinical Endocrinology & Metabolism, vol. 85, no. 10, pp. 3808–3814, 2000. View at Publisher · View at Google Scholar
  18. H. Li, X. Z. Ruan, and S. H. Powis et al., “EPA and DHA reduce LPS-induced inflammation responses in HK-2 cells: evidence for a PPAR-γ-dependent mechanism,” Kidney International, vol. 67, no. 3, pp. 867–874, 2005. View at Publisher · View at Google Scholar · View at PubMed
  19. A. De Paulis, A. Ciccarelli, I. Marinò, G. De Crescenzo, D. Marinò, and G. Marone, “Human synovial mast cells: II. heterogeneity of the pharmacologic effects of antiinflammatory and immunosuppressive drugs,” Arthritis and Rheumatism, vol. 40, no. 3, pp. 469–478, 1997. View at Publisher · View at Google Scholar
  20. H. Fahmi, J. A. Di Battista, J. P. Pelletier, F. Mineau, P. Ranger, and J. Martel-Pelletier, “Peroxisome proliferator-activated receptor γ activators inhibit interleukin-1β-induced nitric oxide and matrix metalloproteinase 13 production in human chondrocytes,” Arthritis & Rheumatism, vol. 44, no. 3, pp. 595–607, 2001. View at Publisher · View at Google Scholar
  21. Y. Barak, M. C. Nelson, and E. S. Ong et al., “PPAR γ is required for placental, cardiac, and adipose tissue development,” Molecular Cell, vol. 4, no. 4, pp. 585–595, 1999. View at Publisher · View at Google Scholar
  22. V. Sapin, L. Blanchon, A. F. Serre, D. Lemery, B. Dastugue, and S. J. Ward, “Use of transgenic mice model for understanding the placentation: towards clinical applications in human obstetrical pathologies?,” Transgenic Research, vol. 10, no. 5, pp. 377–398, 2001. View at Publisher · View at Google Scholar
  23. P. Antonson, G. U. Schuster, and L. Wang et al., “Inactivation of the nuclear receptor coactivator RAP250 in mice results in placental vascular dysfunction,” Molecular and Cellular Biology, vol. 23, no. 4, pp. 1260–1268, 2003. View at Publisher · View at Google Scholar
  24. Y. Zhu, C. Qi, Y. Jia, J. S. Nye, M. S. Rao, and J. K. Reddy, “Deletion of PBP/PARBP, the gene for nuclear receptor coactivator peroxisome proliferator-activated receptor-binding protein, results in embryonic lethality,” Journal of Biological Chemistry, vol. 275, no. 20, pp. 14779–14782, 2000. View at Publisher · View at Google Scholar · View at PubMed
  25. Y.-J. Zhu, S. E. Crawford, and V. Stellmach et al., “Coactivator PRIP, the peroxisome proliferator-activated receptor-interacting protein, is a modulator of placental, cardiac, hepatic, and embryonic development,” Journal of Biological Chemistry, vol. 278, no. 3, pp. 1986–1990, 2003. View at Publisher · View at Google Scholar · View at PubMed
  26. Y. Barak, D. Liao, and W. He et al., “Effects of peroxisome proliferator-activated receptor δ on placentation, adiposity, and colorectal cancer,” Proceedings of the National Academy of Sciences of the United States of America, vol. 99, no. 1, pp. 303–308, 2002. View at Publisher · View at Google Scholar · View at PubMed
  27. W. T. Schaiff, F. F. Knapp Jr., Y. Barak, T. Biron-Shental, D. M. Nelson, and Y. Sadovsky, “Ligand-activated PPARγ alters placental morphology and placental fatty acid uptake in mice,” Endocrinology, vol. 148, no. 8, pp. 3625–3634, 2007. View at Publisher · View at Google Scholar
  28. W. T. Schaiff, I. Bildirici, M. Cheong, P. L. Chern, D. M. Nelson, and Y. Sadovsky, “Peroxisome proliferator-activated receptor-γ and retinoid X receptor signaling regulate fatty acid uptake by primary human placental trophoblasts,” Journal of Clinical Endocrinology and Metabolism, vol. 90, no. 7, pp. 4267–4275, 2005. View at Publisher · View at Google Scholar · View at PubMed
  29. I. Bildirici, C.-R. Roh, W. T. Schaiff, B. M. Lewkowski, D. M. Nelson, and Y. Sadovsky, “The lipid droplet-associated protein adipophilin is expressed in human trophoblasts and is regulated by peroxisomal proliferator-activated receptor-γ/Retinoid X Receptor,” Journal of Clinical Endocrinology and Metabolism, vol. 88, no. 12, pp. 6056–6062, 2003. View at Publisher · View at Google Scholar
  30. A. K. Duttaroy, “Fetal growth and development: roles of fatty acid transport proteins and nuclear transcription factors in human placenta,” Indian Journal of Experimental Biology, vol. 42, no. 8, pp. 747–757, 2004.
  31. M. Lappas, K. Yee, M. Permezel, and G. E. Rice, “Lipopolysaccharide and TNF-α activate the nuclear factor kappa B pathway in the human placental JEG-3 cells,” Placenta, vol. 27, no. 6-7, pp. 568–575, 2006. View at Publisher · View at Google Scholar · View at PubMed
  32. D. A. Kniss, “Cyclooxygenases in reproductive medicine and biology,” Journal of the Society for Gynecologic Investigation, vol. 6, no. 6, pp. 285–292, 1999. View at Publisher · View at Google Scholar
  33. M. Lappas, M. Permezel, H. M. Georgiou, and G. E. Rice, “Regulation of proinflammatory cytokines in human gestational tissues by peroxisome proliferator-activated receptor-γ: effect of 15-deoxy-Δ12,14-PGJ2 and troglitazone,” Journal of Clinical Endocrinology & Metabolism, vol. 87, no. 10, pp. 4667–4672, 2002. View at Publisher · View at Google Scholar
  34. W. E. Ackerman, X. L. Zhang, B. H. Rovin, and D. A. Kniss, “Modulation of cytokine-induced cyclooxygenase 2 expression by PPARG ligands through NFκB signal disruption in human WISH and amnion cells,” Biology of reproduction, vol. 73, no. 3, pp. 527–535, 2005. View at Publisher · View at Google Scholar · View at PubMed
  35. E. B. Berry, J. A. Keelan, R. J. Helliwell, R. S. Gilmour, and M. D. Mitchell, “Nanomolar and micromolar effects of 15-deoxy- Δ12,14-prostaglandin J2 on amnion-derived wish epithelial cells: differential roles of peroxisome proliferator-activated receptors γ and δ and nuclear factor κB,” Molecular Pharmacology, vol. 68, no. 1, pp. 169–178, 2005. View at Publisher · View at Google Scholar · View at PubMed
  36. M. Lappas and G. E. Rice, “Phospholipase A2 isozymes in pregnancy and parturition,” Prostaglandins Leukotrienes and Essential Fatty Acids, vol. 70, no. 2, pp. 87–100, 2004. View at Publisher · View at Google Scholar
  37. M. Lappas, M. Permezel, and G. E. Rice, “Leptin and adiponectin stimulate the release of proinflammatory cytokines and prostaglandins from human placenta and maternal adipose tissue via nuclear factor-κB, peroxisomal proliferator-activated receptor-γ and extracellularly regulated kinase 1/2,” Endocrinology, vol. 146, no. 8, pp. 3334–3342, 2005. View at Publisher · View at Google Scholar · View at PubMed
  38. L. R. Dunn-Albanese, W. E. Ackerman, Y. Xie, J. D. Iams, and D. A. Kniss, “Reciprocal expression of peroxisome proliferator-activated receptor-γ and cyclooxygenase-2 in human term parturition,” American Journal of Obstetrics and Gynecology, vol. 190, no. 3, pp. 809–816, 2004. View at Publisher · View at Google Scholar · View at PubMed
  39. T. M. Lindstrom and P. R. Bennett, “15-Deoxy-Δ12,14-prostaglandin J2 inhibits interleukin-1β-induced nuclear factor-κb in human amnion and myometrial cells: mechanisms and implications,” Journal of Clinical Endocrinology & Metabolism, vol. 90, no. 6, pp. 3534–3543, 2005. View at Publisher · View at Google Scholar · View at PubMed
  40. L. Capparuccia, D. Marzioni, and A. Giordano et al., “PPARγ expression in normal human placenta, hydatidiform mole and choriocarcinoma,” Molecular Human Reproduction, vol. 8, no. 6, pp. 574–579, 2002. View at Publisher · View at Google Scholar
  41. J. M. Roberts, R. N. Taylor, T. J. Musci, G. M. Rodgers, C. A. Hubel, and M. K. McLaughlin, “Preeclampsia: an endothelial cell disorder,” American Journal of Obstetrics and Gynecology, vol. 161, no. 5, pp. 1200–1204, 1989.
  42. D. Ware Branch, M. D. Mitchell, E. Miller, W. Palinski, and J. L. Witztum, “Pre-eclampsia and serum antibodies to oxidised low-density lipoprotein,” Lancet, vol. 343, no. 8898, pp. 645–646, 1994. View at Publisher · View at Google Scholar
  43. R. D. Johnson, K. L. Polakoski, X. Huang, Y. Sadovsky, and D. M. Nelson, “The release of 15-hydroxyeicosatetraenoic acid by human placental trophoblast is increased in preeclampsia,” American Journal of Obstetrics and Gynecology, vol. 178, no. 1 part 1, pp. 54–58, 1998. View at Publisher · View at Google Scholar
  44. R. L. Schild, W. T. Schaiff, M. G. Carlson, E. J. Cronbach, D. M. Nelson, and Y. Sadovsky, “The activity of PPAR γ in primary human trophoblasts is enhanced by oxidized lipids,” Journal of Clinical Endocrinology and Metabolism, vol. 87, no. 3, pp. 1105–1110, 2002. View at Publisher · View at Google Scholar
  45. T. Fournier, L. Pavan, and A. Tarrade et al., “The role of PPAR-γ/RXR-α heterodimers in the regulation of human trophoblast invasion,” Annals of the New York Academy of Sciences, vol. 973, pp. 26–30, 2002.
  46. J. A. Keelan, T. A. Sato, K. W. Marvin, J. Lander, R. S. Gilmour, and M. D. Mitchell, “15-Deoxy-Δ12,14-prostaglandin J2, a ligand for peroxisome proliferator-activated receptor-γ, induces apoptosis in JEG3 choriocarcinoma cells,” Biochemical and Biophysical Research Communications, vol. 262, no. 3, pp. 579–585, 1999. View at Publisher · View at Google Scholar · View at PubMed
  47. J. Keelan, R. Helliwell, and B. Nijmeijer et al., “15-Δ12,14-prostaglandin J2-induced apoptosis in amnion-like WISH cells,” Prostaglandins and Other Lipid Mediators, vol. 66, no. 4, pp. 265–282, 2001. View at Publisher · View at Google Scholar
  48. S.-Q. Kuang, L. Liao, and H. Zhang et al., “Deletion of the cancer-amplified coactivator AIB3 results in defective placentation and embryonic lethality,” Journal of Biological Chemistry, vol. 277, no. 47, pp. 45356–45360, 2002. View at Publisher · View at Google Scholar · View at PubMed
  49. K. Nadra, S. I. Anghel, and E. Joye et al., “Differentiation of trophoblast giant cells and their metabolic functions are dependent on peroxisome proliferator-activated receptor β/δ,” Molecular and Cellular Biology, vol. 26, no. 8, pp. 3266–3281, 2006. View at Publisher · View at Google Scholar · View at PubMed
  50. L. Julan, H. Guan, J. P. Van Beek, and K. Yang, “Peroxisome proliferator-activated receptor δ suppresses 11β-hydroxysteroid dehydrogenase type 2 gene expression in human placental trophoblast cells,” Endocrinology, vol. 146, no. 3, pp. 1482–1490, 2005. View at Publisher · View at Google Scholar · View at PubMed
  51. Y. Xu, T. J. Cook, and G. T. Knipp, “Effects of di-(2-ethylhexyl)-phthalate (DEHP) and its metabolites on fatty acid homeostasis regulating proteins in rat placental HRP-1 trophoblast cells,” Toxicological Sciences , vol. 84, no. 2, pp. 287–300, 2005. View at Publisher · View at Google Scholar · View at PubMed
  52. E. Capobianco, A. Jawerbaum, V. White, C. Pustovrh, D. Sinner, and E. T. Gonzalez, “Elevated levels of endothelin-1 and prostaglandin E2 and their effect on nitric oxide generation in placental tissue from neonatal streptozotocin-induced diabetic rats,” Prostaglandins Leukotrienes and Essential Fatty Acids, vol. 68, no. 3, pp. 225–231, 2003. View at Publisher · View at Google Scholar
  53. A. Jawerbaum, E. Capobianco, and C. Pustovrh et al., “Influence of peroxisome proliferator-activated receptor γ activation by its endogenous ligand 15-deoxy Δ12,14 prostaglandin J2 on nitric oxide production in term placental tissues from diabetic women,” Molecular Human Reproduction, vol. 10, no. 9, pp. 671–676, 2004. View at Publisher · View at Google Scholar · View at PubMed
  54. A. Jawerbaum and E. González, “Diabetic pregnancies: the challenge of developing in a pro-inflammatory environment,” Current Medicinal Chemistry, vol. 13, no. 18, pp. 2127–2138, 2006. View at Publisher · View at Google Scholar
  55. M. J. Willi, M. Winkler, D.-C. Fischer, T. Reineke, H. Maul, and W. Rath, “Chorioamnionitis: elevated interleukin-6 and interleukin-8 concentrations in the lower uterine segment,” Journal of Perinatal Medicine, vol. 30, no. 4, pp. 292–296, 2002. View at Publisher · View at Google Scholar · View at PubMed
  56. V. Zaga, G. Estrada-Gutierrez, J. Beltran-Montoya, R. Maida-Claros, R. Lopez-Vancell, and F. Vadillo-Ortega, “Secretions of interleukin-1β and tumor necrosis factor α by whole fetal membranes depend on initial interactions of amnion or choriodecidua with lipopolysaccharides or group B streptococci,” Biology of Reproduction, vol. 71, no. 4, pp. 1296–1302, 2004. View at Publisher · View at Google Scholar · View at PubMed
  57. B. Jacobsson, I. Mattsby-Baltzer, and H. Hagberg, “Interleukin-6 and interleukin-8 in cervical and amniotic fluid: relationship to microbial invasion of the chorioamniotic membranes,” Journal of Obstetrics and Gynaecology, vol. 112, no. 6, pp. 719–724, 2005. View at Publisher · View at Google Scholar · View at PubMed
  58. V. Zaga-Clavellina, G. G. Lopez, and G. Estrada-Gutierrez et al., “Incubation of human chorioamniotic membranes with Candida albicans induces differential synthesis and secretion of interleukin-1β, interleukin-6, prostaglandin E2, and 92 kDa type IV collagenase,” Mycoses, vol. 49, no. 1, pp. 6–13, 2006. View at Publisher · View at Google Scholar · View at PubMed
  59. B. Toth, D. Hornung, C. Scholz, S. Djalali, K. Friese, and U. Jeschke, “Peroxisome proliferator-activated receptors: new players in the field of reproduction,” American Journal of Reproductive Immunology, vol. 58, no. 3, pp. 289–310, 2007. View at Publisher · View at Google Scholar · View at PubMed