MEMBRANE DEPOLARIZATION INHIBITS KV1.5 VOLTAGE-GATED K-TRANSCRIPTION AND PROTEIN EXPRESSION IN PITUITARY-CELLS( CHANNEL GENE)

Citation
Es. Levitan et al., MEMBRANE DEPOLARIZATION INHIBITS KV1.5 VOLTAGE-GATED K-TRANSCRIPTION AND PROTEIN EXPRESSION IN PITUITARY-CELLS( CHANNEL GENE), The Journal of biological chemistry, 270(11), 1995, pp. 6036-6041
Citations number
43
Categorie Soggetti
Biology
ISSN journal
00219258
Volume
270
Issue
11
Year of publication
1995
Pages
6036 - 6041
Database
ISI
SICI code
0021-9258(1995)270:11<6036:MDIKVK>2.0.ZU;2-D
Abstract
Voltage-gated K+ channels play an essential role in the production of action potential activity by excitable cells, Recent studies have sugg ested that expression of K+ channel genes may be regulated by stimuli that affect electrical activity. Elevating the concentration of extrac ellular KCl causes membrane depolarization and, thus, is widely used f or 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 E v1.4 and Rv2.1 mRNA levels, K+ channel blockers, which cause depolariz ation, also produce down-regulation of Kv1.5 mRNA, while NaCl addition had no effect. Thus, the effect of KCl is mediated by K+-induced memb rane depolarization. Unlike many known effects of K down-regulation of Kv1.5 mRNA does not require Ca2+ or Na+ influx, or Na+-H+ exchange. F urthermore, the decrease in Kv1.5 mRNA expression is due to inhibition of channel gene transcription and persists after inhibition of protei n synthesis, excluding a role for induction of intermediary regulatory proteins. Finally, immunoblots with antibody specific for the Kv1.5 p olypeptide show that depolarization for 8 h reduces the expression of Kv1.5 channel protein. The decrease in K+ channel protein expression c aused by depolarization-induced Ca2+-independent inhibition of Kv1.5 g ene transcription may produce a longterm enhancement of pituitary cell excitability and secretory activity.