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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Connexin-based gap junction hemichannels: Gating mechanisms
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Connexin-based gap junction hemichannels: Gating mechanisms

机译:基于连接蛋白的间隙连接半通道:门控机制

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摘要

Connexins (Cxs) form hemichannels and gap junction channels. Each gap junction channel is composed of two hemichannels, also termed connexons, one from each of the coupled cells. Hemichannels are hexamers assembled in the ER, the Golgi, or a post Golgi compartment. They are transported to the cell surface in vesicles and inserted by vesicle fusion, and then dock with a hemichannel in an apposed membrane to form a cell-cell channel. It was thought that hemichannels should remain closed until docking with another hemichannel because of the leak they would provide if their permeability and conductance were like those of their corresponding cell-cell channels. Now it is clear that hemichannels formed by a number of different connexins can open in at least some cells with a finite if low probability, and that their opening can be modulated under various physiological and pathological conditions. Hemichannels open in different kinds of cells in culture with conductance and permeability properties predictable from those of the corresponding gap junction channels. Cx43 hemichannels are preferentially closed in cultured cells under resting conditions, but their open probability can be increased by the application of positive voltages and by changes in protein phosphorylation and/or redox state. In addition, increased activity can result from the recruitment of hemichannels to the plasma membrane as seen in metabolically inhibited astrocytes. Mutations of connexins that increase hemichannel open probability may explain cellular degeneration in several hereditary diseases. Taken together, the data indicate that hemichannels are gated by multiple mechanisms that independently or cooperatively affect their open probability under physiological as well as pathological conditions. (c) 2005 Elsevier B.V. All rights reserved.
机译:连接蛋白(Cxs)形成半通道和间隙连接通道。每个间隙连接通道由两个半通道组成,也称为连接子,每个耦合单元中都有一个。半通道是在ER,高尔基体或后高尔基体隔室中组装的六聚体。它们被运输到囊泡中的细胞表面并通过囊泡融合插入,然后与半通道对接在对置的膜中以形成细胞-细胞通道。人们认为,半通道应保持封闭,直到与另一个半通道对接为止,因为如果它们的渗透性和电导率与其相应的细胞-细胞通道相似,它们将提供泄漏。现在清楚的是,由许多不同的连接蛋白形成的半通道可以以至少有限的概率在至少一些细胞中打开,并且可以在各种生理和病理条件下调节它们的打开。半通道在培养的不同种类的细胞中开放,其电导率和渗透性可从相应的间隙连接通道中预测到。 Cx43半通道在静止条件下优先在培养的细胞中关闭,但可以通过施加正电压以及通过蛋白质磷酸化和/或氧化还原状态的变化来增加其打开概率。另外,如在代谢抑制的星形胶质细胞中所见,半通道募集至质膜可导致活性增加。连接蛋白的突变会增加半通道开放的可能性,这可能解释了几种遗传性疾病中的细胞变性。综上所述,数据表明半通道是由多种机制控制的,这些机制在生理和病理条件下独立或共同影响其开放概率。 (c)2005 Elsevier B.V.保留所有权利。

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