A G-protein-activated inwardly rectifying K+ channel (GIRK4) from human hippocampus associates with other GIRK channels

被引:1
|
作者
Spauschus, A
Lentes, KU
Wischmeyer, E
Dissmann, E
Karschin, C
Karschin, A
机构
[1] MAX PLANCK INST BIOPHYS CHEM,D-37077 GOTTINGEN,GERMANY
[2] MAX PLANCK INST EXPTL MED,D-37077 GOTTINGEN,GERMANY
来源
JOURNAL OF NEUROSCIENCE | 1996年 / 16卷 / 03期
关键词
inwardly rectifying K+ channels; K-ATP channels; GIRK; G-protein-activation hetero-oligomers; heterologous expression; hippocampus;
D O I
暂无
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Transcripts of a gene, GIRK4, that encodes for a 419-amino-acid protein and shows high structural similarity to other subfamily members of G-protein-activated inwardly rectifying K+ channels (GIRK) have been identified in the human hippocampus. When expressed in Xenopus oocytes, GIRK4 yielded functional GIRK channels with activity that was enhanced by the stimulation of coexpressed serotonin 1A receptors. GIRK4 potentiated basal and agonist-induced currents mediated by other GIRK channels, possibly because of channel heteromerization. Despite the structural similarity to a putative rat K-ATP channel, no ATP sensitivity or K-ATP-typical pharmacology was observed for GIRK4 alone or GIRK4 transfected in conjunction with other GIRK channels in COS-7 cells. In rat brain, GIRK4 is expressed together with three other subfamily members, GIRK1-3, most likely in identical hippocampal neurons. Thus, heteromerization or an unknown molecular interaction may cause the physiological diversity observed within this class of K+ channels.
引用
收藏
页码:930 / 938
页数:9
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