Interaction between mineralocorticoid receptor and cAMP/CREB signaling

Steroids. 2010 Aug-Sep;75(8-9):539-43. doi: 10.1016/j.steroids.2009.10.006. Epub 2009 Oct 30.

Abstract

Besides regulating water and electrolyte homeostasis, the mineralocorticoid receptor (MR) elicits pathophysiological effects in the renocardiovascular system. Although the MR's closest relative, the glucocorticoid receptor (GR), acts as a transcription factor at the same hormone-response-element (HRE), activated glucocorticoid receptor mediates very different effects. One explanation for this discrepancy is that the MR interacts with additional signaling pathways in the cytosol. In the literature, there are several indications for an interaction between aldosterone/MR and the cAMP/CREB signaling. Here we summarize the current knowledge of the cross-talk between the two signaling pathways, including some unpublished observations of our own that indicate that MR/CREB signaling is mediated by calcineurin and has potentially pathophysiological consequences.

Publication types

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

MeSH terms

  • Animals
  • Calcineurin / metabolism
  • Cyclic AMP / metabolism*
  • Cyclic AMP Response Element-Binding Protein / metabolism*
  • Humans
  • Receptors, Mineralocorticoid / metabolism*
  • Signal Transduction*

Substances

  • Cyclic AMP Response Element-Binding Protein
  • Receptors, Mineralocorticoid
  • Cyclic AMP
  • Calcineurin