Discordant effects of corticosteroids and expression of subunits on ENaC activity

Am J Physiol Renal Physiol. 2007 Sep;293(3):F813-20. doi: 10.1152/ajprenal.00225.2007. Epub 2007 Jul 3.

Abstract

In renal distal nephron and airway epithelial cells, adrenocortical steroids increase epithelial Na+ channel (ENaC) activity and also markedly increase the expression of the alpha-subunit. The present experiments were designed to reconstitute this steroid effect in ENaC-expressing cells by overexpressing the subunits whose expression is enhanced by corticosteroids. In renal collecting duct monolayers, corticosteroids increased ENaC activity 5- to 8-fold, endogenous alpha-ENaC mRNA and protein approximately 10-fold, and beta-ENaC protein and mRNA 1.2- to 2-fold. gamma-ENaC expression was unchanged. To determine whether this increase in expression was sufficient to increase ENaC activity, we used a regulated adenovirus system to increase expression of each subunit alone and in combination. Unexpectedly, increased expression of the alpha- and/or beta-subunit had no effect on ENaC activity in collecting duct cells or lung epithelial cells. In contrast, a small increase in gamma-ENaC expression increased ENaC activity about threefold. This increase in activity was additive to the effect of steroids. Thus, even though corticosteroids strongly increase alpha-ENaC expression and moderately increase beta-ENaC expression, these effects are not, by themselves, sufficient to increase ENaC activity. Knockdown experiments are consistent with the idea that the increased expression of alpha-ENaC is necessary for the full steroid effect on ENaC. Increased expression of gamma-ENaC and corticosteroid treatment enhances ENaC activity by parallel, noninteracting pathways. These results underscore the importance of other actions of steroid hormones for long-term enhancement of ENaC activity and raise new possibilities for regulation of ENaC activity by gamma-ENaC expression.

Publication types

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

MeSH terms

  • Aldosterone / pharmacology*
  • Animals
  • Biological Transport, Active / drug effects
  • Biological Transport, Active / physiology
  • Cell Line
  • Dexamethasone / pharmacology*
  • Epithelial Sodium Channels / chemistry
  • Epithelial Sodium Channels / genetics
  • Epithelial Sodium Channels / metabolism*
  • Gene Expression Regulation / drug effects*
  • Humans
  • Protein Subunits / genetics*
  • Protein Subunits / metabolism*
  • Rats
  • Sodium / metabolism

Substances

  • Epithelial Sodium Channels
  • Protein Subunits
  • Aldosterone
  • Dexamethasone
  • Sodium