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异聚体和同聚体Cx40及Cx43连接子之间的异型间隙连接通道形成。

Heterotypic gap junction channel formation between heteromeric and homomeric Cx40 and Cx43 connexons.

作者信息

Cottrell G T, Burt J M

机构信息

Department of Physiology, Arizona Health Sciences Center, University of Arizona, Tucson, Arizona 85724, USA.

出版信息

Am J Physiol Cell Physiol. 2001 Nov;281(5):C1559-67. doi: 10.1152/ajpcell.2001.281.5.C1559.

Abstract

Recent evidence indicating formation of functional homomeric/heterotypic gap junction channels by connexin40 (Cx40) and connexin43 (Cx43) raises the question of whether data previously interpreted as support for heteromeric channel formation by these connexins might not instead reflect the activity of homomeric/heterotypic channels. To address this question and to further characterize the behavior of these channels, we used dual whole cell voltage-clamp techniques to examine the junctions formed between cells that express only Cx40 (Rin40) or Cx43 (Rin43) and compared the results with those obtained when either of these cell types was paired with cells that naturally express both connexins (A7r5 cells). Rin40/Rin43 cell pairs formed functional gap junctions that displayed a strongly asymmetric voltage-dependent gating response. Single-channel event amplitudes ranged between 34 and 150 pS, with 90- to 130-pS events predominating. A7r5/Rin43 and A7r5/Rin40 cell pairs had voltage-dependent gating responses that varied greatly, with most pairs demonstrating strong asymmetry. These cell pairs exhibited a variety of single-channel events that were not consistent with homomeric/homotypic Cx40 or Cx43 channels or homomeric/heterotypic Cx40/Cx43 channels. These data indicate that Cx40 and Cx43 form homomeric/heterotypic as well as heteromeric/heterotypic channels that display unique gating and conductance properties.

摘要

最近有证据表明,连接蛋白40(Cx40)和连接蛋白43(Cx43)可形成功能性同型/异型缝隙连接通道,这就提出了一个问题:之前被解释为支持这些连接蛋白形成异型通道的数据,是否可能反而反映了同型/异型通道的活性。为了解决这个问题并进一步表征这些通道的行为,我们使用双全细胞膜片钳技术来检测仅表达Cx40(Rin40)或Cx43(Rin43)的细胞之间形成的连接,并将结果与这些细胞类型中的任何一种与天然同时表达这两种连接蛋白的细胞(A7r5细胞)配对时获得的结果进行比较。Rin40/Rin43细胞对形成了功能性缝隙连接,表现出强烈的不对称电压依赖性门控反应。单通道事件幅度在34至150 pS之间,以90至130 pS的事件为主。A7r5/Rin43和A7r5/Rin40细胞对具有差异很大的电压依赖性门控反应,大多数细胞对表现出强烈的不对称性。这些细胞对表现出各种单通道事件,这些事件与同型/同型Cx40或Cx43通道或同型/异型Cx40/Cx43通道不一致。这些数据表明,Cx40和Cx43形成了具有独特门控和电导特性的同型/异型以及异型/异型通道。

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