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双膜间隙连接内化需要网格蛋白介导的内吞机制。

Double-membrane gap junction internalization requires the clathrin-mediated endocytic machinery.

作者信息

Gumpert Anna M, Varco Joseph S, Baker Susan M, Piehl Michelle, Falk Matthias M

机构信息

Department of Biological Sciences, Lehigh University, 111 Research Drive, Bethlehem, PA 18015, USA.

出版信息

FEBS Lett. 2008 Aug 20;582(19):2887-92. doi: 10.1016/j.febslet.2008.07.024. Epub 2008 Jul 24.

Abstract

Direct cell-cell communication mediated by plasma membrane-spanning gap junction (GJ) channels is vital to all aspects of cellular life. Obviously, GJ intercellular communication (GJIC) requires precise regulation, and it is known that controlled biosynthesis and degradation, and channel opening and closing (gating) are exploited. We discovered that cells internalize GJs in response to various stimuli. Here, we report that GJ internalization is a clathrin-mediated endocytic process that utilizes the vesicle-coat protein clathrin, the adaptor proteins adaptor protein complex 2 and disabled 2, and the GTPase dynamin. To our knowledge, we are first to report that the endocytic clathrin machinery can internalize double-membrane vesicles into cells.

摘要

由跨质膜的间隙连接(GJ)通道介导的直接细胞间通讯对细胞生命的各个方面都至关重要。显然,GJ细胞间通讯(GJIC)需要精确调控,已知其利用了受控的生物合成与降解以及通道的开放与关闭(门控)。我们发现细胞会响应各种刺激而内化GJ。在此,我们报告GJ内化是一种网格蛋白介导的内吞过程,该过程利用了囊泡包被蛋白网格蛋白、衔接蛋白衔接蛋白复合物2和失活蛋白2以及GTP酶发动蛋白。据我们所知,我们首次报道内吞网格蛋白机制可将双膜囊泡内化到细胞中。

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