Caveolin-1 potentiates estrogen receptor alpha (ERalpha) signaling. caveolin-1 drives ligand-independent nuclear translocation and activation of ERalpha

J Biol Chem. 1999 Nov 19;274(47):33551-6. doi: 10.1074/jbc.274.47.33551.

Abstract

Estrogen receptor alpha (ERalpha) is a soluble protein that mediates the effects of the gonadal estrogens such as 17beta-estradiol. Upon ligand binding, a cytoplasmic pool of ERalpha translocates to the nucleus, where it acts as a transcription factor, driving the expression of genes that contain estrogen-response elements. The activity of ERalpha is regulated by a number of proteins, including cytosolic chaperones and nuclear cofactors. Here, we show that caveolin-1 potentiates ERalpha-mediated signal transduction. Coexpression of caveolin-1 and ERalpha resulted in ligand-independent translocation of ERalpha to the nucleus as shown by both cell fractionation and immunofluorescence microscopic studies. Similarly, caveolin-1 augmented both ligand-independent and ligand-dependent ERalpha signaling as measured using a estrogen-response element-based luciferase reporter assay. Caveolin-1-mediated activation of ERalpha was sensitive to a well known ER antagonist, 4-hydroxytamoxifen. However, much higher concentrations of tamoxifen were required to mediate inhibition in the presence of caveolin-1. Interestingly, caveolin-1 expression also synergized with a constitutively active, ligand-independent ERalpha mutant, dramatically illustrating the potent stimulatory effect of caveolin-1 in this receptor system. Taken together, our results identify caveolin-1 as a new positive regulator of ERalpha signal transduction.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Biological Transport
  • Caveolin 1
  • Caveolins*
  • Cell Nucleus / metabolism*
  • Estrogen Receptor alpha
  • Humans
  • Ligands
  • Membrane Proteins / metabolism
  • Membrane Proteins / physiology*
  • Protein Binding
  • Receptors, Estrogen / agonists
  • Receptors, Estrogen / metabolism*
  • Signal Transduction / physiology*
  • Tumor Cells, Cultured

Substances

  • CAV1 protein, human
  • Caveolin 1
  • Caveolins
  • Estrogen Receptor alpha
  • Ligands
  • Membrane Proteins
  • Receptors, Estrogen