Inside the Endometrial Cell Signaling Subway: Mind the Gap(s)

Int J Mol Sci. 2018 Aug 21;19(9):2477. doi: 10.3390/ijms19092477.

Abstract

Endometrial cells perceive and respond to their microenvironment forming the basis of endometrial homeostasis. Errors in endometrial cell signaling are responsible for a wide spectrum of endometrial pathologies ranging from infertility to cancer. Intensive research over the years has been decoding the sophisticated molecular means by which endometrial cells communicate to each other and with the embryo. The objective of this review is to provide the scientific community with the first overview of key endometrial cell signaling pathways operating throughout the menstrual cycle. On this basis, a comprehensive and critical assessment of the literature was performed to provide the tools for the authorship of this narrative review summarizing the pivotal components and signaling cascades operating during seven endometrial cell fate "routes": proliferation, decidualization, implantation, migration, breakdown, regeneration, and angiogenesis. Albeit schematically presented as separate transit routes in a subway network and narrated in a distinct fashion, the majority of the time these routes overlap or occur simultaneously within endometrial cells. This review facilitates identification of novel trajectories of research in endometrial cellular communication and signaling. The meticulous study of endometrial signaling pathways potentiates both the discovery of novel therapeutic targets to tackle disease and vanguard fertility approaches.

Keywords: angiogenesis; breakdown; decidualization; endometrial cell; implantation; migration; pathway; proliferation; regeneration.

Publication types

  • Review

MeSH terms

  • Blastocyst / cytology
  • Blastocyst / metabolism
  • Cell Differentiation
  • Cell Proliferation
  • Embryo Implantation / physiology
  • Endometrium / cytology
  • Endometrium / metabolism*
  • Female
  • Fertility / genetics*
  • Gene Expression Regulation
  • Homeostasis / genetics
  • Humans
  • Intercellular Signaling Peptides and Proteins / genetics*
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Menstrual Cycle / physiology
  • Neovascularization, Physiologic / genetics
  • Signal Transduction*
  • Stromal Cells / cytology
  • Stromal Cells / metabolism*
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism

Substances

  • Intercellular Signaling Peptides and Proteins
  • Transcription Factors