Non-genomic regulation of vascular cell function and growth by estrogen

Mol Cell Endocrinol. 2009 Sep 24;308(1-2):9-16. doi: 10.1016/j.mce.2009.03.009. Epub 2009 Mar 25.

Abstract

Estrogens exert rapid, non-genomic effects, which are mediated by plasma membrane-associated estrogen receptors (mER) mERalpha and mERbeta, and the intracellular transmembrane G protein-coupled estrogen receptor (GPER). Membrane-initiated responses contribute to transcriptional activation, resulting in a complex interplay of nuclear and extra-nuclear mechanisms that mediate the acute physiological responses to estrogens. Non-genomic estrogen signaling also activates a variety of intracellular estrogen signaling pathways that regulate vascular function and cell growth involving rapid but also long-term effects. This review discusses recent advances in understanding of the mechanisms of non-genomic estrogen receptor signaling in the vascular wall.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Actins / metabolism
  • Animals
  • Cell Survival
  • Cytoskeleton / metabolism
  • Endothelial Cells / physiology*
  • Estrogens / metabolism*
  • Gene Expression Regulation
  • Humans
  • Receptors, Estrogen / metabolism
  • Receptors, G-Protein-Coupled / metabolism
  • Signal Transduction / physiology*

Substances

  • Actins
  • Estrogens
  • Receptors, Estrogen
  • Receptors, G-Protein-Coupled