Division of Molecular and Cellular Pharmacology, Department of Pharmacology, Graduate School of Medicine, Osaka University, 2-2 Yamada-oka, Suita, Osaka, 565-0871, Japan.
Pflugers Arch. 2010 Mar;459(4):521-33. doi: 10.1007/s00424-009-0754-z. Epub 2009 Dec 11.
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.
耳蜗内淋巴液是一种含有 150mM K(+)的细胞外溶液,呈现出+80mV 的正电势。这个正电势被称为内淋巴液(endocochlear potential,EP),是听觉的基础。自首次测量以来,半个世纪以来,负责形成 EP 的机制一直是个谜。一个关键元素是血管纹,它具有独特的组织结构,并表达多种离子转运装置。血管纹由两层上皮细胞组成:一层是边缘细胞,另一层由中间细胞和基底细胞组成。在这两层之间是一个被称为内淋巴间隙(intrastrial space,IS)的细胞外空间,因此它被中间细胞的顶膜和边缘细胞的基底外侧膜所包围。IS 中的液体具有低浓度的 K(+)和类似于 EP 的正电势。我们已经证明,IS 与相邻的细胞外液(外淋巴液)和内淋巴液在电学上是隔离的,这使得 IS 能够维持其正电势。这种 IS 电势是由 K(+)通过中间细胞的顶膜扩散产生的,其中内向整流 Kir4.1 通道定位在此处。IS 中的低 K(+)浓度是维持大 K(+)-扩散电势所必需的,这是由边缘细胞基底外侧膜上表达的 Na(+)、K(+)-ATP 酶和 Na(+)、K(+)、2Cl(-)-共转运体维持的。由边缘细胞顶膜上的 KCNQ1/KCNE1-K(+)通道形成的另一个 K(+)-扩散电势也有助于 EP 的形成。因此,EP 依赖于血管纹中的一个电学隔离空间和两个 K(+)-扩散电势。