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首页> 外文期刊>Pfluegers Archiv: European Journal of Physiology >How is the highly positive endocochlear potential formed? The specific architecture of the stria vascularis and the roles of the ion-transport apparatus.
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How is the highly positive endocochlear potential formed? The specific architecture of the stria vascularis and the roles of the ion-transport apparatus.

机译:高度正向的耳蜗内电位如何形成?血管纹的具体结构和离子传输装置的作用。

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摘要

Cochlear endolymph, an extracellular solution containing 150 mM K(+), exhibits a positive potential of +80 mV. This is called the endocochlear potential (EP) and is essential for audition. The mechanism responsible for formation of the EP has been an enigma for the half century since its first measurement. A key element is the stria vascularis, which displays a characteristic tissue structure and expresses multiple ion-transport apparatus. The stria comprises two epithelial layers: a layer of marginal cells and one composed of intermediate and basal cells. Between the two layers lies an extracellular space termed the intrastrial space (IS), which is thus surrounded by the apical membranes of intermediate cells and the basolateral membranes of marginal cells. The fluid in the IS exhibits a low concentration of K(+) and a positive potential similar to the EP. We have demonstrated that the IS is electrically isolated from the neighboring extracellular fluids, perilymph, and endolymph, which allows the IS to sustain its positive potential. This IS potential is generated by K(+) diffusion across the apical membranes of intermediate cells, where inwardly rectifying Kir4.1 channels are localized. The low K(+) concentration in the IS, which is mandatory for the large K(+)-diffusion potential, is maintained by Na(+),K(+)-ATPases and Na(+),K(+),2Cl(-)-cotransporters expressed at the basolateral membranes of marginal cells. An additional K(+)-diffusion potential formed by KCNQ1/KCNE1-K(+) channels at the apical membranes of marginal cells also contributes to the EP. Therefore, the EP depends on an electrically isolated space and two K(+)-diffusion potentials in the stria vascularis.
机译:耳蜗内淋巴,一种包含150 mM K(+)的细胞外溶液,显示+80 mV的正电位。这被称为耳蜗内电位(EP),对于试听来说是必不可少的。自首次测量以来,造成EP形成的机制一直是一个谜。关键因素是血管纹,显示出特征性的组织结构并表达多种离子转运装置。纹状体包括两层上皮层:一层边缘细胞和一层由中间和基底细胞组成。在两层之间是称为胞内空间(IS)的细胞外空间,该空间因此被中间细胞的顶膜和边缘细胞的基底外侧膜所包围。 IS中的流体表现出低的K(+)浓度和类似于EP的正电势。我们已经证明,IS与邻近的细胞外液,周淋巴和内淋巴电隔离,这使IS可以保持其正电位。该IS电位是由K(+)扩散穿过中间细胞的顶膜而形成的,其中向内整流的Kir4.1通道位于其中。 Na(+),K(+)-ATPases和Na(+),K(+)维持IS中低的K(+)浓度,这对于大的K(+)扩散潜力是必不可少的。 2Cl(-)-cotransporters在边缘细胞的基底外侧膜表达。由KCNQ1 / KCNE1-K(+)通道在边缘细胞的顶膜形成的额外K(+)扩散潜力也有助于EP。因此,EP取决于电隔离空间和血管纹中的两个K(+)扩散电位。

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