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用ryanodine和咖啡因处理后,柯蒂氏器支持细胞中的缝隙连接变化

Gap junction change in supporting cells of the organ of Corti with ryanodine and caffeine.

作者信息

Sato Y, Handa T, Matsumura M, Orita Y

机构信息

Sato ENT Clinic (Okayama), Japan.

出版信息

Acta Otolaryngol. 1998 Nov;118(6):821-5. doi: 10.1080/00016489850182512.

Abstract

It has been demonstrated that the gap junctions of the supporting cells of the organ of Corti are controlled by H+ and Ca2+. Inside these cells there is a tubular structure. It is supposed that this network is endoplasmic reticulum. Calcium release from inside the cells, and the effect of calcium on the gap junctions of these cells, were investigated under whole cell clamping application of ryanodine and caffeine. Membrane capacitance and membrane resistance were calculated, with corrections for changes in whole cell parameters. Ryanodine-treated cells (1 microM-10 mM), caffeine-treated cells (5 mM 500 nM) and A23187-treated cells were uncoupled at their gap junctions. Therefore, Ca2+ plays a role in the uncoupling of the gap junctions in supporting cells of the organ of Corti from inside the cells.

摘要

已证实,柯蒂氏器支持细胞的缝隙连接受H⁺和Ca²⁺控制。这些细胞内部有一个管状结构。据推测,这个网络是内质网。在应用ryanodine和咖啡因进行全细胞钳制的情况下,研究了细胞内钙的释放以及钙对这些细胞缝隙连接的影响。计算了膜电容和膜电阻,并对全细胞参数的变化进行了校正。用ryanodine处理的细胞(1微摩尔 - 10毫摩尔)、用咖啡因处理的细胞(5毫摩尔 - 500纳摩尔)和用A23187处理的细胞在其缝隙连接处解偶联。因此,Ca²⁺在柯蒂氏器支持细胞内缝隙连接的解偶联中起作用。

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