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January 18, 2026Endocrinology0 citations

Emerging Roles of Progesterone Receptor Membrane Components in Pregnancy and Parturition

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JSJessica O SelimLRLauren RichardsonRMRamkumar Menon

Key Points

  • This review aims to clarify the roles of progesterone receptor membrane components 1 and 2 in pregnancy and parturition.
  • Comprehensive narrative review of existing literature
  • Analysis of functional roles of PGRMC1 and PGRMC2
  • Evaluation of their interactions with heme and cytochrome P450 enzymes.
  • PGRMC1 and PGRMC2 function as multi-ligand regulators in gestational tissues.
  • Distinct roles in heme biology and metabolism have been highlighted.
  • Contribution to progesterone signaling in maternal and fetal organs has been detailed.

Abstract

Abstract Progesterone receptor membrane components 1 and 2 (PGRMC1 and PGRMC2) are single-pass proteins that function as multi-ligand regulators. They integrate signals from progesterone (P4), heme, and cytochrome P450 enzymes (CYPs). Accumulating evidence implicates PGRMCs in non-genomic progesterone signaling in cell, cancer and reproductive biology. Heme binding (through their heme binding domain) and cytochrome P450 enzymes (CYPs) binding provide distinct functional roles for PGRMCs in various cells under specific cellular environment. In reproductive tissues, multiple functional roles have been reported for both PGRMC1 and PGRMC2 in both maternal and fetal organs. Ambiguity still exists about their independent functional role and contributions in pregnancy maintenance or initiation of parturition. Collectively, PGRMC1 and PGRMC2 act in complementary ways to regulate heme biology, metabolism, and P4-responsive signaling in gestational tissues. With the growing interest in PGRMC’s role in pregnancy associated tissues, we provide a comprehensive narrative of PGRMCs through this review to facilitate future research and stimulate continued discussions.

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Cite This Study

Selim et al. (2026) studied this question.

synapsesocial.com/papers/696c77afeb60fb80d1395de6https://doi.org/10.1210/endocr/bqag007
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