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通过蛋白酶体、内溶酶体和吞噬溶酶体途径降解连接蛋白。

Degradation of connexins through the proteasomal, endolysosomal and phagolysosomal pathways.

机构信息

Cancer Biology Program, University of Hawaii Cancer Center, University of Hawaii at Manoa, 651 Ilalo Street, BSB 222, Honolulu, HI 96813, USA.

出版信息

J Membr Biol. 2012 Jul;245(7):389-400. doi: 10.1007/s00232-012-9461-3. Epub 2012 Jul 8.

DOI:10.1007/s00232-012-9461-3
PMID:22772442
Abstract

Connexins comprise gap junction channels, which create a direct conduit between the cytoplasms of adjacent cells and provide for intercellular communication. Therefore, the level of total cellular connexin protein can have a direct influence on the level of intercellular communication. Control of connexin protein levels can occur through different mechanisms during the connexin life cycle, such as by regulation of connexin gene expression and turnover of existing protein. The degradation of connexins has been extensively studied, revealing proteasomal, endolysosomal and more recently autophagosomal degradation mechanisms that modulate connexin turnover and, subsequently, affect intercellular communication. Here, we review the current knowledge of connexin degradation pathways.

摘要

间隙连接蛋白构成间隙连接通道,在相邻细胞的细胞质之间形成直接的通道,从而实现细胞间通讯。因此,细胞总连接蛋白的水平可以直接影响细胞间通讯的水平。在连接蛋白的生命周期中,可以通过不同的机制来控制连接蛋白的水平,例如调节连接蛋白基因的表达和现有蛋白的周转率。连接蛋白的降解已经得到了广泛的研究,揭示了蛋白酶体、内溶酶体和最近的自噬体降解机制,这些机制调节连接蛋白的周转率,从而影响细胞间通讯。在这里,我们回顾了连接蛋白降解途径的最新知识。

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Degradation of connexins through the proteasomal, endolysosomal and phagolysosomal pathways.通过蛋白酶体、内溶酶体和吞噬溶酶体途径降解连接蛋白。
J Membr Biol. 2012 Jul;245(7):389-400. doi: 10.1007/s00232-012-9461-3. Epub 2012 Jul 8.
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本文引用的文献

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Internalized gap junctions are degraded by autophagy.细胞内缝隙连接被自噬降解。
Autophagy. 2012 May 1;8(5):794-811. doi: 10.4161/auto.19390.
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The gap junction channel protein connexin 43 is covalently modified and regulated by SUMOylation.间隙连接通道蛋白连接蛋白 43 被 SUMO 化共价修饰和调节。
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Connexins: substrates and regulators of autophagy.连接蛋白:自噬的底物与调节因子
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Protein kinase Cδ-mediated phosphorylation of Connexin43 gap junction channels causes movement within gap junctions followed by vesicle internalization and protein degradation.蛋白激酶 Cδ介导的缝隙连接蛋白 43 通道磷酸化导致缝隙连接内的运动,随后是囊泡内化和蛋白降解。
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FEBS Lett. 2014 Apr 17;588(8):1221-9. doi: 10.1016/j.febslet.2014.01.031. Epub 2014 Jan 30.
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Proteins and mechanisms regulating gap-junction assembly, internalization, and degradation.调节间隙连接组装、内化和降解的蛋白质和机制。
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Activation of Akt, not connexin 43 protein ubiquitination, regulates gap junction stability.激活 Akt,而非连接蛋白 43 蛋白泛素化,调节缝隙连接稳定性。
J Biol Chem. 2012 Jan 20;287(4):2600-7. doi: 10.1074/jbc.M111.276261. Epub 2011 Dec 2.
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Road to ruin: targeting proteins for degradation in the endoplasmic reticulum.走向毁灭:内质网中靶向蛋白质降解。
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Endocytosis and post-endocytic sorting of connexins.连接蛋白的内吞作用及内吞后分选
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