Skip to main content
Log in

Decreased expression of progesterone receptor membrane component 1 in fetal membranes with chorioamnionitis among women with preterm birth

  • Maternal-Fetal Medicine
  • Published:
Archives of Gynecology and Obstetrics Aims and scope Submit manuscript

Abstract

Purpose

Progesterone receptor membrane component 1 (PGRMC1) have anti-inflammatory and anti-apoptotic properties. This study aimed to determine the expression of PGRMC1 in fetal membranes among women with preterm labor (PTL), preterm premature rupture of membranes (PPROM), and acute histologic chorioamnionitis (HCA) during preterm birth.

Methods

Full thickness fetal membranes were obtained from women with gestational age-matched (32–34 weeks of gestational age), and categorized as PTL without HCA (PTL, n = 10), PPROM without HCA (PPROM, n = 10), PPROM with HCA (HCA, n = 10), and term without labor and HCA (term birth (TB), n = 9). The expression of PGRMC1 was assessed using western blot and Immunohistochemistry (IHC). As CD14 is a component of the innate immune system during inflammation, CD14 was used as inflammatory indicator. Nonparametric statistics were used for analysis.

Results

PGRMC1 expression for all of preterm birth was lower than in TB (P = 0.01). In HCA, PGRMC1 expression was significantly decreased compared to that in PTL and PPROM (P = 0.006. P = 0.001, respectively). PGRMC1 expression in PPROM was higher than that in PTL (P = 0.002). There was a negative correlation between PGRMC1 and CD 14/β-actin ratio (r = − 0.518; P = 0.002). IHC showed that PGRMC1 was predominant in the cytoplasm of cells, these results were consistent with those of the western blot analysis.

Conclusion

Preterm birth with PTL, PPROM, and especially HCA is associated with a decreased PGRMC1 in fetal membranes and inversely associated with increased CD 14.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Mesiano S, Wang Y, Norwit ER (2011) Progesterone receptors in the human pregnancy uterus: do they hold the key to birth timing? Reprod Sci 18(1):6–19. https://doi.org/10.1177/1933719110382922

    Article  CAS  PubMed  Google Scholar 

  2. Valadez-Cosmes P, Vázquez-Martínez ER, Cerbón M et al (2016) Membrane progesterone receptors in reproduction and cancer. Mol Cell Endocrinol 15(434):166–175. https://doi.org/10.1016//j.mce.2016.06.027

    Article  Google Scholar 

  3. Merlino A, Welsh T, Erdonmez T et al (2009) Nuclear progesterone receptor expression in the human fetal membranes and deciduas at term before and after labor. Reprod Sci 16(4):357–363. https://doi.org/10.1177//1933719108328616

    Article  CAS  PubMed  Google Scholar 

  4. Thomas P (2008) Characteristics of membrane progestin receptor alpha (mPRα) and progesterone membrane receptor component one (PGRMC1) and their roles in mediating rapid progestin actions. Front Neuroendocrinol 29(2):292–312. https://doi.org/10.1016/j.yfrne.2008.01.001

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Garg D, Ng SSM, Baig KM et al (2017) Progesterone-mediated non-classical signaling. Trends Endocrinol Metab 28(9):656–668. https://doi.org/10.1016/j.tem.2017.05.006

    Article  CAS  PubMed  Google Scholar 

  6. Peluso JJ, Romak J, Liu X (2008) Progesterone receptor membrane component-1 (PGRMC1) is the mediator of progesterone’s antiapoptotic action in spontaneously immortalized granulosa cells as revealed by PGRMC1 small interfering ribonucleic acid treatment and functional analysis of PGRMC1 mutations. Endocrinology 149(2):534–543. https://doi.org/10.1210/en.2007-1050

    Article  CAS  PubMed  Google Scholar 

  7. Peluso JJ, Liu X, Gawkowska A et al (2010) Progesterone inhibits apoptosis in part by PGRMC1-regulated gene expression. Mol Cell Endocrinol 320(14):153–161. https://doi.org/10.1016/j.mce.2010.02.005

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Allen TK, Feng L, Grotegut CA et al (2014) Progesterone receptor membrane component 1 as the mediator of inhibitory effect of progestins on cytokine-induced matrix metalloproteinase 9 activity in vitro. Reprod Sci 21(2):260–268. https://doi.org/10.1177/1933719113493514

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Schwartz N, Xue X, Elovitz MA et al (2009) Progesterone suppression the fetal inflammatory response ex vivo. Am J Obstet Gynecol 201(2):211.e1–e9. https://doi.org/10.1016/jajog.2009.05.012

    Article  Google Scholar 

  10. Feng L, Ransom CE, Nazzal MK et al (2016) The role of progesterone and a novel progesterone receptor, progesterone receptor membrane component 1, in the inflammatory response of fetal membranes to Ureaplasma parvum infection. PLoS ONE 11(12):e0168102. https://doi.org/10.1371/journal.pone.0168102

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Feng L, Antczak BC, Lan L et al (2014) Progesterone receptor membrane component 1(PGRMC1) expression in fetal membranes among women with preterm premature rupture of membranes (PPROM). Placenta 35(5):331–333. https://doi.org/10.1016/j.placenta.2014.03.008

    Article  CAS  PubMed  Google Scholar 

  12. Meng Y, Murtha AP, Feng L (2016) Progesterone, inflammatory cytokine (TNF- α), and oxidative stress (H2O2) regulate progesterone receptor membrane component 1 expression in fetal membrane cells. Reprod Sci 23(9):1168–1178. https://doi.org/10.1177/1933719116630412

    Article  CAS  PubMed  Google Scholar 

  13. Wu W, Shi SQ, Huang HJ et al (2011) Changes in PGRMC1, a potential progesterone receptor, in human myometrium during pregnancy and labour at term and preterm. Mol Hum Reprod 17(4):233–242. https://doi.org/10.1093/molehr/gaq096

    Article  CAS  PubMed  Google Scholar 

  14. Tapping RI (2009) Innate immune sensing and activation of cell surface Toll-like receptors. Semin Immunol 21(4):175–184. https://doi.org/10.1016/j.smim.2009.05.003

    Article  CAS  PubMed  Google Scholar 

  15. Gardella C, Hitti J, Martin TR et al (2001) Amniotic fluid lipopolysaccharide-binding protein and soluble CD 14 as mediators of the inflammatory response in preterm labor. Am J Obstet Gynecol 184(6):1241–1248. https://doi.org/10.1067/mob.2001.113908

    Article  CAS  PubMed  Google Scholar 

  16. Martinez-Lopez DG, Funderburg NT, Cerissi A et al (2014) Lipopolysaccharide and soluble CD14 in cord blood plasma are associated with prematurity and chorioamnionitis. Pediatr Res 75(1-1):67–74. https://doi.org/10.1038/pr.2013.182

    Article  CAS  PubMed  Google Scholar 

  17. Kim CJ, Romero R, Chaemsaithong P et al (2015) Acute chorioamnionitis and funisitis: definition, pathologic features, and clinical significance. Am J Obstet Gynecol 213(4Suppl):S29–S52. https://doi.org/10.1016/j.ajog.2015.08.040

    Article  PubMed  PubMed Central  Google Scholar 

  18. Goldenberg RL, Culhane JF, Iams JD et al (2008) Epidemiology and causes of preterm birth. Lancet 5(371):75–84. https://doi.org/10.1016/S0140-6736(08)60074-4

    Article  Google Scholar 

  19. Redline RW (2015) Classification of placental lesions. Am J Obstet Gynecol 213(4 Suppl):S21–S28. https://doi.org/10.1016/j.ajog.2015.05.056

    Article  PubMed  Google Scholar 

  20. Feng L, Allen TK, Marinello WP et al (2019) Roles of progesterone receptor membrane component 1 in oxidative stress-induced aging in chorion cells. Reprod Sci 26(3):394–403. https://doi.org/10.1177/1933719118776790

    Article  CAS  PubMed  Google Scholar 

  21. Faas MM, Spaans F, De Vos P (2014) Monocytes and macrophages in pregnancy and pre-eclampsia. Front Immunol 30(5):298. https://doi.org/10.3389/fimmu.2014.00298

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We would like to thank Ji Young Seo for laboratory work.

Funding

This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government [No. 2017R1D1A1B03029882].

Author information

Authors and Affiliations

Authors

Contributions

SRC: Protocol/Project development, Data collection and analysis, Manuscript writing. HEC, EJ, HYC, SJ and SJ: collect the fetal membranes. SJC: examin histologic findings and IHC staining of fetal membranes. SOH: Manuscript editing.

Corresponding author

Correspondence to Soo Ran Choi.

Ethics declarations

Conflict of interest

The authors declare no conflicts of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Choi, S.R., Choi, H.E., Jo, E. et al. Decreased expression of progesterone receptor membrane component 1 in fetal membranes with chorioamnionitis among women with preterm birth. Arch Gynecol Obstet 301, 949–954 (2020). https://doi.org/10.1007/s00404-020-05476-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00404-020-05476-8

Keywords

Navigation