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KCNQ1 is the luminal K+ recycling channel during stimulation of gastric acid secretion

机译:KCNQ1是刺激胃酸分泌过程中的腔内K +循环通道

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摘要

Parietal cell (PC) proton secretion via H+/K+-ATPase requires apical K+ recycling. A variety of K+ channels and transporters are expressed in the PC and the molecular nature of the apical K+ recycling channel is under debate. This study was undertaken to delineate the exact function of KCNQ1 channels in gastric acid secretion. Acid secretory rates and electrophysiological parameters were determined in gastric mucosae of 7- to 8-day-old KCNQ1~(+/+), ~(+/-) and ~(-/-) mice. Parietal cell ultrastructure, abundance and gene expression levels were quantified. Glandular structure and PC abundance, and housekeeping gene expression did not differ between the KCNQl~(-/-) and ~(+/+) mucosae. Microvillar secretory membranes were intact, but basal acid secretion was absent and forskolin-stimulated acid output reduced by ~90% in KCNQ1~(-/-) gastric mucosa. Application of a high K~+ concentration to the luminal membrane restored normal acid secretory rates in the KCNQ1~(-/-) mucosa. The study demonstrates that the KCNQ1 channel provides K~+ to the extracellular K~+ binding site of the H~+/K~+-ATPase during acid secretion, and no other gastric K~+ channel can substitute for this function.
机译:通过H + / K + -ATPase分泌顶细胞(PC)的质子需要顶端K +回收。 PC中表达了多种K +通道和转运蛋白,而顶端K +再循环通道的分子性质仍在争论中。进行这项研究来描述KCNQ1通道在胃酸分泌中的确切功能。测定了7至8天大的KCNQ1〜(+ / +),〜(+/-)和〜(-/-)小鼠的胃黏膜中的酸分泌率和电生理参数。壁细胞超微结构,丰度和基因表达水平进行了量化。 KCNQ1〜(-/-)和〜(+ / +)黏膜之间的腺结构和PC丰度以及管家基因表达没有差异。 KCNQ1〜(-/-)胃黏膜中微绒毛的分泌膜完好无损,但缺乏基础酸分泌,福司可林刺激的酸输出减少了约90%。在管腔膜上施加高浓度的K〜+可恢复KCNQ1〜(-/-)粘膜的正常酸分泌率。研究表明,在酸分泌过程中,KCNQ1通道向H〜+ / K〜+ -ATPase的胞外K〜+结合位点提供K〜+,并且没有其他胃K〜+通道可以替代此功能。

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