Membrane cholesterol extraction decreases Na+ transport in A6 renal epithelia

Am J Physiol Cell Physiol. 2006 Jan;290(1):C87-94. doi: 10.1152/ajpcell.00184.2005. Epub 2005 Aug 17.

Abstract

In this study, we have investigated the dependence of Na+ transport regulation on membrane cholesterol content in A6 renal epithelia. We continuously monitored short-circuit current (Isc), transepithelial conductance (GT), and transepithelial capacitance (CT) to evaluate the effects of cholesterol extraction from the apical and basolateral membranes in steady-state conditions and during activation with hyposmotic shock, oxytocin, and adenosine. Cholesterol extraction was achieved by perfusing the epithelia with methyl-beta-cyclodextrin (mbetaCD) for 1 h. In steady-state conditions, apical membrane cholesterol extraction did not significantly affect the electrophysiological parameters; in contrast, marked reductions were observed during basolateral mbetaCD treatment. However, apical mbetaCD application hampered the responses of Isc and GT to hypotonicity, oxytocin, and adenosine. Analysis of the blocker-induced fluctuation in Isc demonstrated that apical mbetaCD treatment decreased the epithelial Na+ channel (ENaC) open probability (Po) in the steady state as well as after activation of Na+ transport by adenosine, whereas the density of conducting channels was not significantly changed as confirmed by CT measurements. Na+ transport activation by hypotonicity was abolished during basolateral mbetaCD treatment as a result of reduced Na+/K+ pump activity. On the basis of the findings in this study, we conclude that basolateral membrane cholesterol extraction reduces Na+/K+ pump activity, whereas the reduced cholesterol content of the apical membranes affects the activation of Na+ transport by reducing ENaC Po.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine / pharmacology
  • Animals
  • Artifacts
  • Cell Line
  • Cell Polarity / physiology
  • Cholesterol / metabolism*
  • Epithelial Cells / cytology
  • Epithelial Cells / metabolism*
  • Epithelial Sodium Channels
  • Hypotonic Solutions / pharmacology
  • Ion Channel Gating / drug effects
  • Ion Channel Gating / physiology
  • Kidney / cytology*
  • Membrane Lipids / metabolism*
  • Osmotic Pressure
  • Oxytocin / pharmacology
  • Potassium / metabolism
  • Sodium / metabolism*
  • Sodium Channels / metabolism
  • Sodium-Potassium-Exchanging ATPase / metabolism
  • Xenopus laevis
  • beta-Cyclodextrins / pharmacology

Substances

  • Epithelial Sodium Channels
  • Hypotonic Solutions
  • Membrane Lipids
  • Sodium Channels
  • beta-Cyclodextrins
  • methyl-beta-cyclodextrin
  • Oxytocin
  • Cholesterol
  • Sodium
  • Sodium-Potassium-Exchanging ATPase
  • Adenosine
  • Potassium