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间隙连接通道的化学门控;钙、pH值和钙调蛋白的作用。

Chemical gating of gap junction channels; roles of calcium, pH and calmodulin.

作者信息

Peracchia Camillo

机构信息

Department of Pharmacology and Physiology, University of Rochester, School of Medicine and Dentistry, Rochester, NY 14642-8711, USA.

出版信息

Biochim Biophys Acta. 2004 Mar 23;1662(1-2):61-80. doi: 10.1016/j.bbamem.2003.10.020.

DOI:10.1016/j.bbamem.2003.10.020
PMID:15033579
Abstract

Both Ca(2+) and H(+) play a role in chemical gating of gap junction channels, but, with the possible exception of Cx46 hemichannels, neither of them is likely to induce gating by a direct interaction with connexins. Some evidence suggests that low pH(i) affects gating via an increase in Ca(2+); in turn, Ca(2+) is likely to induce gating by activation of CaM, which may act directly as a gating particle. The effective concentrations of both Ca(2+) and H(+) vary depending on cell type, type of connexin expressed and procedure employed to increase their cytosolic concentrations; however, pH(i) as high as 7.2 and Ca(2+) as low as 150 nM or lower have been reported to be effective in some cells. Some data suggest that Ca(2+) and H(+) affect gating by acting synergistically, but other data do not support synergism. Chemical gating follows the activation of a slow gate distinct from the fast V(j)-sensitive gate, and there is evidence that the chemical/slow gate is V(j)-sensitive. At the single channel level, the chemical/slow gate closes the channels slowly and completely, whereas the fast V(j) gate closes the channels rapidly and incompletely. At least three molecular models of channel gating have been proposed, but all of them are mostly based on circumstantial evidence.

摘要

Ca(2+)和H(+)在间隙连接通道的化学门控中均发挥作用,但除了Cx46半通道可能是个例外,它们都不太可能通过与连接蛋白的直接相互作用来诱导门控。一些证据表明,低pH(i)通过增加Ca(2+)来影响门控;反过来,Ca(2+)可能通过激活钙调蛋白来诱导门控,钙调蛋白可能直接作为门控颗粒起作用。Ca(2+)和H(+)的有效浓度因细胞类型、所表达的连接蛋白类型以及用于增加其胞质浓度的方法而异;然而,据报道,在某些细胞中,pH(i)高达7.2以及Ca(2+)低至150 nM或更低时是有效的。一些数据表明,Ca(2+)和H(+)通过协同作用影响门控,但其他数据并不支持协同作用。化学门控遵循与快速V(j)敏感门不同的慢门的激活,并且有证据表明化学/慢门对V(j)敏感。在单通道水平上,化学/慢门将通道缓慢且完全关闭,而快速V(j)门将通道快速且不完全关闭。至少已经提出了三种通道门控的分子模型,但所有这些模型大多基于间接证据。

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