Membrane depolarization inhibits Kv1.5 voltage-gated K+ channel gene transcription and protein expression in pituitary cells

J Biol Chem. 1995 Mar 17;270(11):6036-41. doi: 10.1074/jbc.270.11.6036.

Abstract

Voltage-gated K+ channels play an essential role in the production of action potential activity by excitable cells. Recent studies have suggested that expression of K+ channel genes may be regulated by stimuli that affect electrical activity. Elevating the concentration of extracellular KCl causes membrane depolarization and, thus, is widely used for studying electrical activity-dependent changes in neurons, muscle, and endocrine cells. Here we show that elevated KCl decreases Kv1.5 K+ channel mRNA expression in clonal pituitary cells without affecting Kv1.4 and Kv2.1 mRNA levels. K+ channel blockers, which cause depolarization, also produce down-regulation of Kv1.5 mRNA, while NaCl addition had no effect. Thus, the effect of KCl is mediated by K(+)-induced membrane depolarization. Unlike many known effects of K+, down-regulation of Kv1.5 mRNA does not require Ca2+ or Na+ influx, or Na(+)-H+ exchange. Furthermore, the decrease in Kv1.5 mRNA expression is due to inhibition of channel gene transcription and persists after inhibition of protein synthesis, excluding a role for induction of intermediary regulatory proteins. Finally, immunoblots with antibody specific for the Kv1.5 polypeptide show that depolarization for 8 h reduces the expression of Kv1.5 channel protein. The decrease in K+ channel protein expression caused by depolarization-induced Ca(2+)-independent inhibition of Kv1.5 gene transcription may produce a long-term enhancement of pituitary cell excitability and secretory activity.

Publication types

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

MeSH terms

  • Amiloride / pharmacology
  • Animals
  • Calcium / metabolism
  • Clone Cells
  • Down-Regulation / physiology
  • Gene Expression* / drug effects
  • Kv1.5 Potassium Channel
  • Meglumine / pharmacology
  • Membrane Potentials / physiology*
  • Nifedipine / pharmacology
  • Nimodipine / pharmacology
  • Pituitary Neoplasms
  • Potassium Channels / biosynthesis*
  • Potassium Channels, Voltage-Gated*
  • Potassium Chloride / pharmacology*
  • Protein Biosynthesis
  • RNA, Messenger / metabolism
  • Rats
  • Sodium / metabolism
  • Sodium-Hydrogen Exchangers / metabolism
  • Transcription, Genetic* / drug effects
  • Tumor Cells, Cultured

Substances

  • Kcna5 protein, rat
  • Kv1.5 Potassium Channel
  • Potassium Channels
  • Potassium Channels, Voltage-Gated
  • RNA, Messenger
  • Sodium-Hydrogen Exchangers
  • Nimodipine
  • Potassium Chloride
  • Meglumine
  • Amiloride
  • Sodium
  • Nifedipine
  • Calcium