cAMP stimulation of CFTR-expressing Xenopus oocytes activates a chromanol-inhibitable K+ conductance

Pflugers Arch. 1996 Jul;432(3):516-22. doi: 10.1007/s004240050164.

Abstract

Cystic fibrosis transmembrane conductance regulator (CFTR) functions as a Cl- channel in a large variety of cells expressing this protein. Recently evidence has accumulated that it also regulates other ion channels. A coordinated increase in Cl- and K+ conductances is necessary in many Cl--secreting epithelia. This has, for example, recently been demonstrated for the colonic crypt, for which a new type of K+ channel and a specific inhibitor of this channel, the chromanol 293B, have been described. In the present study we have examined whether the cAMP-evoked activation of CFTR, overexpressed in Xenopus oocytes, in addition to its known activation of a Cl- conductance, also upregulates endogenous K+ channels. It is shown that CFTR-cRNA-injected but not water-injected oocytes possess a cAMP-activated Cl- conductance. Of the cAMP-induced whole-cell current increase, 15-25% was due to a 293B-, Ba2+and TEA+-inhibitable K+ conductance. The cRNA of the mutated CFTR (DeltaF508 CFTR) had no such effect. We conclude that cAMP activated CFTR and an endogenous IsK-type and 293B-sensitive K+ conductance. Similar events, occurring, for example, in the colonic crypt possessing CFTR and 293B-sensitive K+ channels, might explain the coordinated cAMP-mediated increase in Cl- and K+ conductances.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Methyl-3-isobutylxanthine / pharmacology
  • Animals
  • Antioxidants / pharmacology*
  • Biotransformation / drug effects
  • Chromans / pharmacology*
  • Cyclic AMP / analogs & derivatives
  • Cyclic AMP / pharmacology*
  • Cystic Fibrosis Transmembrane Conductance Regulator / biosynthesis*
  • Oocytes / drug effects
  • Oocytes / metabolism*
  • Patch-Clamp Techniques
  • Phosphodiesterase Inhibitors / pharmacology
  • Phosphorylation
  • Potassium Channels / drug effects
  • Potassium Channels / metabolism*
  • Tetraethylammonium Compounds / pharmacology
  • Thionucleotides / pharmacology
  • Xenopus laevis

Substances

  • Antioxidants
  • Chromans
  • Phosphodiesterase Inhibitors
  • Potassium Channels
  • Tetraethylammonium Compounds
  • Thionucleotides
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • 8-((4-chlorophenyl)thio)cyclic-3',5'-AMP
  • 2,2,5,7,8-pentamethyl-1-hydroxychroman
  • Cyclic AMP
  • 1-Methyl-3-isobutylxanthine