Cyclic AMP regulates potassium channel expression in C6 glioma by destabilizing Kv1.1 mRNA

被引:26
作者
Allen, ML
Koh, DS
Tempel, BL
机构
[1] Univ Washington, Sch Med, Virginia Verrill Bloedel Hearing Res Ctr, Seattle, WA 98195 USA
[2] Univ Washington, Sch Med, Dept Pharmacol, Seattle, WA 98195 USA
[3] Univ Washington, Sch Med, Dept Physiol & Biophys, Seattle, WA 98195 USA
[4] Univ Washington, Sch Med, Dept Otolaryngol, Seattle, WA 98195 USA
关键词
gene expression; translational regulation; glia;
D O I
10.1073/pnas.95.13.7693
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The tissue distributions and physiological properties of a variety of cloned voltage-gated potassium channel genes have been characterized extensively, yet relatively little is known about the mechanisms controlling expression of these genes. Here, we report studies on the regulation of Kv1.1 expressed endogenously in the C6 glioma cell line. We demonstrate that elevation of intracellular cAMP leads to the accelerated degradation of Kv1.1 RNA. The cAMP-induced decrease in Kv1.1 RNA is followed by a decrease in Kv1.1 protein and a decrease in the whole cell sustained Kf current amplitude. Dendrotoxin-I, a relatively specific blocker of Kv1.1 blocks 96% of the sustained K+ current in glioma cells, causing a shift in the resting membrane potential from -40 mV to -7 mV, These data suggest that expression of Kv1.1 contributes to setting the resting membrane potential in undifferentiated glioma cells, We therefore suggest that receptor-mediated elevation of cAMP reduces outward K+ current density by acting at the translational level to destabilize Kv1.1 RNA, an additional mechanism for regulating potassium channel gene expression.
引用
收藏
页码:7693 / 7698
页数:6
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