Aldosterone does not alter apical cell-surface expression of epithelial Na+ channels in the amphibian cell line A6

J Biol Chem. 1992 May 15;267(14):9622-8.

Abstract

The steroid hormone aldosterone regulates reabsorptive Na+ transport across specific high resistance epithelia. The increase in Na+ transport induced by aldosterone is dependent on protein synthesis and is due, in part, to an increase in Na+ conductance of the apical membrane mediated by amiloride-sensitive Na+ channels. To examine whether an increment in the biochemical pool of Na+ channels expressed at the apical cell surface is a mechanism by which aldosterone increases apical membrane Na+ conductance, apical cell-surface proteins from the epithelial cell line A6 were specifically labeled by an enzyme-catalyzed radioiodination procedure following exposure of cells to aldosterone. Labeled Na+ channels were immunoprecipitated to quantify the biochemical pool of Na+ channels at the apical cell surface. The activation of Na+ transport across A6 cells by aldosterone was not accompanied by alterations in the biochemical pool of Na+ channels at the apical plasma membrane, despite a 3.7-4.2-fold increase in transepithelial Na+ transport. Similarly, no change in the distribution of immunoreactive protein was resolved by immunofluorescence microscopy. The oligomeric subunit composition of the channel remained unaltered, with one exception. A 75,000-Da polypeptide and a broad 70,000-Da polypeptide were observed in controls. Following addition of aldosterone, the 75,000-Da polypeptide was not resolved, and the 70,000-Da polypeptide was the major polypeptide found in this molecular mass region. Aldosterone did not alter rates of Na+ channel biosynthesis. These data suggest that neither changes in rates of Na+ channel biosynthesis nor changes in its apical cell-surface expression are required for activation of transepithelial Na+ transport by aldosterone. Post-translational modification of the Na+ channel, possibly the 75,000 or 70,000-Da polypeptide, may be one of the cellular events required for Na+ channel activation by aldosterone.

Publication types

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

MeSH terms

  • Aldosterone / pharmacology*
  • Animals
  • Cell Line
  • Electrophoresis, Polyacrylamide Gel
  • Epithelium / metabolism
  • Kidney
  • Kinetics
  • Macromolecular Substances
  • Membrane Potentials / drug effects
  • Membrane Proteins / biosynthesis*
  • Membrane Proteins / isolation & purification
  • Methionine / metabolism
  • Molecular Weight
  • Sodium Channels / drug effects
  • Sodium Channels / metabolism*
  • Spironolactone / pharmacology
  • Sulfur Radioisotopes
  • Xenopus laevis

Substances

  • Macromolecular Substances
  • Membrane Proteins
  • Sodium Channels
  • Sulfur Radioisotopes
  • Spironolactone
  • Aldosterone
  • Methionine