首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >A G-protein-activated inwardly rectifying K+ channel (GIRK4) from human hippocampus associates with other GIRK channels.
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A G-protein-activated inwardly rectifying K+ channel (GIRK4) from human hippocampus associates with other GIRK channels.

机译:来自人海马的G蛋白激活的内向整流K +通道(GIRK4)与其他GIRK通道相关。

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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 KATP channel, no ATP sensitivity or KATP-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 classof K+ channels.
机译:已经在人海马体中发现了一个编码419个氨基酸的蛋白的基因GIRK4的转录本,该转录本与G蛋白激活的内向整流K +通道(GIRK)的其他亚家族成员表现出高度的结构相似性。当在非洲爪蟾卵母细胞中表达时,GIRK4产生功能性GIRK通道,其活性通过刺激共表达的血清素1A受体而增强。 GIRK4增强了由其他GIRK通道介导的基础和激动剂诱导的电流,这可能是由于通道的异构化。尽管与假定的大鼠KATP通道在结构上相似,但在COS-7细胞中,对于单独的GIRK4或与其他GIRK通道一起转染的GIRK4,未观察到ATP敏感性或KATP典型药理学。在大鼠大脑中,GIRK4与其他三个亚家族成员GIRK1-3一起表达,最有可能在相同的海马神经元中表达。因此,异构化或未知的分子相互作用可能导致在此类K +通道内观察到的生理多样性。

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