首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >An ATP-dependent inwardly rectifying potassium channel, KAB-2 (Kir4. 1), in cochlear stria vascularis of inner ear: its specific subcellular localization and correlation with the formation of endocochlear potential.
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An ATP-dependent inwardly rectifying potassium channel, KAB-2 (Kir4. 1), in cochlear stria vascularis of inner ear: its specific subcellular localization and correlation with the formation of endocochlear potential.

机译:内耳的耳蜗纹状血管中一个依赖ATP的内向整流钾通道KAB-2(Kir4.1。):其特定的亚细胞定位及其与耳蜗内电位的形成相关。

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摘要

Cochlear endolymph has a highly positive potential of approximately +80 mV. This so-called endocochlear potential (EP) is essential for hearing. Although pivotal roles of K+ channels in the formation of EP have been suggested, the types and distribution of K+ channels in cochlea have not been characterized. Because EP was depressed by vascular perfusion of Ba2+, an inhibitor of inwardly rectifying K+ (Kir) channels, but not by either 4-aminopyridine or tetraethylammonium, we examined the expression of Kir channel subunits in cochlear stria vascularis, the tissue that is supposed to play the central role in the generation of positive EP. Of 11 members of the Kir channel family examined with reverse transcription-PCR, we could detect only expression of KAB-2 (Kir4.1) mRNA in stria vascularis. KAB-2 immunoreactivity was specifically localized at the basolateral membrane of marginal cells but not in either basal or intermediate cells. Developmental expression of KAB-2 in marginal cells paralleled formationof EP. Furthermore, deaf mutant mice (viable dominant spotting; WV/WV) expressed no KAB-2 in their marginal cells. These results suggest that KAB-2 in marginal cells may be critically involved in the generation of positive EP.
机译:耳蜗内淋巴具有约+80 mV的高度正电位。这种所谓的耳蜗内电位(EP)对听力至关重要。尽管已经提出了K +通道在EP形成中的关键作用,但是尚未表征耳蜗中K +通道的类型和分布。由于EP通过向内整流K +(Kir)通道的抑制剂Ba2 +的血管灌注而被抑制,但没有被4-氨基吡啶或四乙铵所抑制,因此我们检查了耳蜗纹状体血管组织中Kir通道亚基的表达在产生积极的EP中起核心作用。在逆转录-PCR检查的11个Kir通道家族成员中,我们只能检测到血管纹中的KAB-2(Kir4.1)mRNA表达。 KAB-2免疫反应性特异性地定位在边缘细胞的基底外侧膜上,而不是在基底细胞或中间细胞中。 KAB-2在边缘细胞中的发育表达与EP的形成平行。此外,聋突变小鼠(可行的显性斑点; WV / WV)在其边缘细胞中未表达KAB-2。这些结果表明,边缘细胞中的KAB-2可能与阳性EP的产生密切相关。

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