NLRP3 promotes endometrial receptivity by inducing epithelial-mesenchymal transition of the endometrial epithelium

Mol Hum Reprod. 2021 Nov 2;27(11):gaab056. doi: 10.1093/molehr/gaab056.

Abstract

Endometrial receptivity is crucial for successful embryo implantation. It is regulated by multiple factors which include ovarian steroid hormones and the immune microenvironment among others. Nod-Like Receptor Pyrins-3 (NLRP3) is a key intracellular pattern-recognition receptor and a critical component of the inflammasome, which plays an essential role in the development of inflammation and of immune responses. However, the physiological functions of NLRP3 in the endometrium remain largely unclear. This study investigated the physiological and pathological significance of NLRP3 in human endometrial epithelial cell during the implantation window. NLRP3 is highly expressed during the mid-proliferative and mid-secretory phases of the human endometrium and transcriptionally up-regulated by estradiol (E2) through estrogen receptor β (ERβ). In addition, NLRP3 promotes embryo implantation and enhances epithelial-mesenchymal transition (EMT) of Ishikawa (IK) cells via both inflammasome-dependent and inflammasome-independent pathways, which might provide a novel insight into endometrial receptivity and embryo implantation. Our findings suggest that NLRP3, which is transcriptionally regulated by E2, induces epithelial-mesenchymal transition of endometrial epithelial cells and promotes embryo adhesion.

Keywords: NLRP3; embryo implantation; endometrial receptivity; epithelial cells; epithelial–mesenchymal transition (EMT).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Cell Adhesion
  • Cell Line, Tumor
  • Coculture Techniques
  • Embryo Implantation* / drug effects
  • Endometrium / drug effects
  • Endometrium / immunology
  • Endometrium / metabolism*
  • Epithelial Cells / drug effects
  • Epithelial Cells / immunology
  • Epithelial Cells / metabolism*
  • Epithelial-Mesenchymal Transition* / drug effects
  • Estradiol / pharmacology
  • Female
  • Healthy Volunteers
  • Humans
  • Inflammasomes / genetics
  • Inflammasomes / metabolism*
  • Mice
  • Mice, Inbred ICR
  • NLR Family, Pyrin Domain-Containing 3 Protein / genetics
  • NLR Family, Pyrin Domain-Containing 3 Protein / metabolism*
  • Pregnancy
  • Signal Transduction
  • Young Adult

Substances

  • Inflammasomes
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • NLRP3 protein, human
  • Nlrp3 protein, mouse
  • Estradiol