Reduction of ionic strength activates single volume-regulated anion channels (VRAC) in endothelial cells

Pflugers Arch. 2000 Jan;439(3):315-20. doi: 10.1007/s004249900186.

Abstract

We have previously shown that a reduction of intracellular ionic strength is involved in the activation of volume-regulated anion channels (VRAC). Here we show in a single-channel study that VRAC can be activated in a cell-attached patch when the cell interior is dialyzed with a solution of decreased ionic strength. For this purpose, bovine pulmonary endothelial (CPAE) cells) were permeabilized with alpha-staphylotoxin (alphaST) which has a molecular weight cut-off size of 2 kDa. If the ionic strength in the bath solution is reduced from 160 mM to 95 mM, single-channel activity is initiated in cell-attached patches sealed before permeabilization. Conductance is outwardly rectifying with approximately 17 pS at negative and 57 pS at positive potentials. Single-channel currents reverse near the calculated equilibrium potential for Cl-. The averaged current shows inactivation at positive potentials. The current is blocked by 5-nitro-2-(3-phenylpropylamino)-benzoic acid (NPPB). An increase in ionic strength reversibly inhibits current activation. It is concluded that a decrease in ionic strength activates single-channel currents through VRAC rather than shifting the set point of a hypothetical volume sensor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anions / metabolism
  • Bacterial Toxins / pharmacology
  • Cattle
  • Cell Adhesion / physiology
  • Cell Membrane Permeability / physiology
  • Cells, Cultured
  • Chloride Channels / physiology
  • Electrophysiology
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / physiology*
  • Endothelium, Vascular / ultrastructure
  • Ion Channel Gating / physiology*
  • Ion Channels / physiology*
  • Ion Channels / ultrastructure
  • Membrane Potentials / physiology
  • Nitrobenzenes / pharmacology
  • Patch-Clamp Techniques
  • Pulmonary Artery / cytology
  • Pulmonary Artery / physiology
  • Pulmonary Artery / ultrastructure
  • Solutions

Substances

  • Anions
  • Bacterial Toxins
  • Chloride Channels
  • Ion Channels
  • Nitrobenzenes
  • Solutions
  • staphylotoxin
  • 5-(4-nitrophenyl)-2,4-pentadienal