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KCNQ1/KCNE通道亚基在小鼠胃肠道中的共定位。

Colocalization of KCNQ1/KCNE channel subunits in the mouse gastrointestinal tract.

作者信息

Dedek K, Waldegger S

机构信息

Zentrum für Molekulare Neurobiologie Hamburg (ZMNH), Hamburg University, Germany.

出版信息

Pflugers Arch. 2001 Sep;442(6):896-902. doi: 10.1007/s004240100609.

Abstract

The KCNQI potassium channel alpha-subunit can associate with various KCNE beta-subunits that drastically influence channel gating. Here we show that in the mouse gastrointestinal tract KCNQ1 is prominently expressed in stomach, small intestine and colon, while KCNE3 is expressed in the colon and to a lesser extent in small intestine. Immunostaining revealed that KCNQ1 colocalizes with KCNE3 in the basolateral membranes of crypt cells of the colon and small intestine. Together with the previously shown electrophysiological properties of KCNQ1/KCNE3 channels, this strongly suggests that they form the basolateral potassium conductance that is required for transepithelial cAMP-stimulated chloride secretion. In the stomach, KCNQ1 is expressed together with the H+/K+-ATPase in the luminal membrane of acid-secreting parietal cells of gastric glands. KCNE2, but neither KCNE1 nor KCNE3 was detected in the stomach by Northern analysis. Similar to KCNQ1, KCNE2 was present in gastric glands in only a subset of cells that probably represent parietal cells. The coexpression of KCNQ1 and KCNE2 in HEK293 cells yielded potassium currents that were open at resting voltages, suggesting that these heteromeric channels may underlie the apical potassium conductance in acid-secreting parietal cells that is necessary for the recycling of potassium ions during acid secretion via the H+/K+-ATPase.

摘要

KCNQ1钾通道α亚基可与多种KCNEβ亚基结合,这些β亚基会极大地影响通道门控。在此我们表明,在小鼠胃肠道中,KCNQ1在胃、小肠和结肠中显著表达,而KCNE3在结肠中表达,在小肠中表达较少。免疫染色显示,KCNQ1与KCNE3在结肠和小肠隐窝细胞的基底外侧膜中共定位。结合先前所示的KCNQ1/KCNE3通道的电生理特性,这有力地表明它们形成了经上皮cAMP刺激的氯离子分泌所需的基底外侧钾电导。在胃中,KCNQ1与H+/K+-ATP酶共同表达于胃腺分泌酸的壁细胞的腔面膜中。通过Northern分析在胃中未检测到KCNE2,也未检测到KCNE1和KCNE3。与KCNQ1相似,KCNE2仅在胃腺中可能代表壁细胞的一部分细胞中存在。KCNQ1和KCNE2在HEK293细胞中的共表达产生了在静息电压下开放的钾电流,这表明这些异源通道可能是分泌酸的壁细胞顶端钾电导的基础,而顶端钾电导是酸分泌过程中通过H+/K+-ATP酶进行钾离子再循环所必需的。

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