Modulation of the volume-sensitive K+ current in Ehrlich ascites tumour cells by pH

Pflugers Arch. 2001 Jul;442(4):622-33. doi: 10.1007/s004240100585.

Abstract

The effects of extracellular and intracellular pH (pHo and pHi respectively) on the regulatory volume decrease (RVD) response and on the volume-sensitive K+ and Cl- currents (IK,vol and ICl,vol respectively) were studied in Ehrlich ascites tumour cells. Alkaline pHo accelerated and acidic pHo decelerated the RVD response significantly. Intra- and extracellular alkalinisation increased the amplitude of IK,vol whereas acidification had an inhibitory effect. The magnitude of ICl,vol was not affected by changes in pHi or pHo. A significant reduction in the activation time for IK,vol after hypotonic cell swelling was observed upon moderate intracellular alkalinisation (to pHi 7.9). A further increase in pHi to 8.4 resulted in the spontaneous activation of an IK under isotonic conditions which resembled IK,vol with respect to its pharmacological profile and current/voltage (I/V) relation. Noise analysis demonstrated that the increased amplitude of IK,vol at alkaline pH resulted mainly from an increase in the number of channels (N) contributing to the current. The channel open probability, Po, was largely unaffected by pH. The pH dependence and the biophysical and pharmacological properties of IK,vol are similar to those of the cloned tandem pore-domain acid-sensitive K+ (TASK) channels, and in the current study the presence of TASK-1 was confirmed in Ehrlich cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkalies
  • Animals
  • Artifacts
  • Buffers
  • Carcinoma, Ehrlich Tumor*
  • Cell Size
  • Chlorides / metabolism
  • Hydrogen-Ion Concentration*
  • Ion Channel Gating / physiology
  • Isotonic Solutions
  • Membrane Potentials / physiology
  • Mice
  • Mice, Inbred Strains
  • Nerve Tissue Proteins*
  • Patch-Clamp Techniques
  • Potassium / metabolism*
  • Potassium Channels / metabolism*
  • Potassium Channels, Tandem Pore Domain*
  • Tumor Cells, Cultured / cytology
  • Tumor Cells, Cultured / metabolism

Substances

  • Alkalies
  • Buffers
  • Chlorides
  • Isotonic Solutions
  • Nerve Tissue Proteins
  • Potassium Channels
  • Potassium Channels, Tandem Pore Domain
  • potassium channel subfamily K member 3
  • Potassium