Progesterone elicits an inhibitory effect upon LPS-induced innate immune response in pre-labor human amniotic epithelium

Am J Reprod Immunol. 2014 Jan;71(1):61-72. doi: 10.1111/aji.12163. Epub 2013 Oct 16.

Abstract

Problem: Infection of human fetal membranes elicits secretion of pro-inflammatory modulators through its innate immune capacities. We investigated the effect of lipopolysacharide (LPS) and progesterone (P4) upon expression of TLR-4/MyD88, TNFα, IL-6, IL-8, IL-10, and HBD2 on the human amniotic epithelium.

Method of study: Explants of the human amniotic epithelium were pre-treated with 0.01, 0.1, and 1.0 μM of P4; then cotreated with 1000 ng/mL LPS. TLR-4 was immuno-detected, and concentrations of MyD88, TNFα, IL-6, IL-8, IL-10, and HBD2 were quantified by ELISA.

Results: P4 significantly reduced the expression of LPS-induced TLR-4/MyD88. LPS increased the concentrations of TNFα, IL-6, IL-8, IL-10, and HBD2 by factors of 30-, eight, three, three, and fivefold, respectively. P4 at 1.0 μM was the most effective dose to blunt the secretion of TNFα, IL-6, and HBD-2. RU-486 blocks the effect of P4.

Conclusion: P4 inhibited LPS-induced TLR-4/MyD88 and pro-inflammatory factors in the human amniotic epithelium. These results could explain partially how P4 can protect the amniotic region of fetal membranes and generate a compensatory mechanism that limits the secretion of pro-inflammatory modulators, which could jeopardize the immune privilege during pregnancy.

Keywords: Chorioamnionitis; TLR-4; human amniotic epithelium; inflammation; innate immunity; progesterone.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amnion / cytology*
  • Cells, Cultured
  • Cytokines / genetics
  • Cytokines / metabolism
  • Epithelium / immunology*
  • Female
  • Gene Expression Regulation
  • Hormone Antagonists / pharmacology
  • Humans
  • Immune Tolerance
  • Immunity, Innate
  • Inflammation Mediators / metabolism
  • Lipopolysaccharides / immunology
  • Mifepristone / pharmacology
  • Myeloid Differentiation Factor 88 / genetics
  • Myeloid Differentiation Factor 88 / metabolism
  • Pregnancy
  • Progesterone / immunology*
  • Toll-Like Receptor 4 / genetics
  • Toll-Like Receptor 4 / metabolism
  • beta-Defensins / genetics
  • beta-Defensins / metabolism

Substances

  • Cytokines
  • DEFB4A protein, human
  • Hormone Antagonists
  • Inflammation Mediators
  • Lipopolysaccharides
  • Myeloid Differentiation Factor 88
  • TLR4 protein, human
  • Toll-Like Receptor 4
  • beta-Defensins
  • Mifepristone
  • Progesterone