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有丝分裂过程中连接蛋白 43 间隙连接蛋白的运输和回收。

Trafficking and recycling of the connexin43 gap junction protein during mitosis.

机构信息

National Center for Microscopy and Imaging Research, Center for Research in Biological Systems, University of California San Diego, La Jolla, CA, USA.

出版信息

Traffic. 2010 Nov;11(11):1471-86. doi: 10.1111/j.1600-0854.2010.01109.x. Epub 2010 Sep 10.

Abstract

During the cell cycle, gap junction communication, morphology and distribution of connexin43 (Cx43)-containing structures change dramatically. As cells round up in mitosis, Cx43 labeling is mostly intracellular and intercellular coupling is reduced. We investigated Cx43 distributions during mitosis both in endogenous and exogenous expressing cells using optical pulse-chase labeling, correlated light and electron microscopy, immunocytochemistry and biochemical analysis. Time-lapse imaging of green fluorescent protein (GFP)/tetracysteine tagged Cx43 (Cx43-GFP-4C) expressing cells revealed an early disappearance of gap junctions, progressive accumulation of Cx43 in cytoplasmic structures, and an unexpected subset pool of protein concentrated in the plasma membrane surrounding the midbody region in telophase followed by rapid reappearance of punctate plaques upon mitotic exit. These distributions were also observed in immuno-labeled endogenous Cx43-expressing cells. Photo-oxidation of ReAsH-labeled Cx43-GFP-4C cells in telophase confirmed that Cx43 is distributed in the plasma membrane surrounding the midbody as apparent connexons and in cytoplasmic vesicles. We performed optical pulse-chase labeling and single label time-lapse imaging of synchronized cells stably expressing Cx43 with internal tetracysteine domains through mitosis. In late telophase, older Cx43 is segregated mainly to the plasma membrane while newer Cx43 is intracellular. This older population nucleates new gap junctions permitting rapid resumption of communication upon mitotic exit.

摘要

在细胞周期中,缝隙连接通讯、连接蛋白 43(Cx43)结构的形态和分布会发生显著变化。在有丝分裂中细胞变圆时,Cx43 的标记主要位于细胞内,细胞间耦联减少。我们使用光学脉冲追踪标记、相关光和电子显微镜、免疫细胞化学和生化分析,研究了内源性和外源性表达细胞中 Cx43 在有丝分裂过程中的分布。绿色荧光蛋白(GFP)/四半胱氨酸标记的 Cx43(Cx43-GFP-4C)表达细胞的延时成像显示,缝隙连接早期消失,Cx43 逐渐积累在细胞质结构中,在有丝分裂末期,一个意想不到的蛋白质亚群集中在围绕着中体的质膜周围,随后在有丝分裂退出时迅速重新出现点状斑块。这些分布也在免疫标记的内源性 Cx43 表达细胞中观察到。在有丝分裂末期,用 ReAsH 标记的 Cx43-GFP-4C 细胞进行光氧化,证实 Cx43 分布在围绕中体的质膜上,作为明显的连接子和细胞质小泡。我们通过有丝分裂对稳定表达具有内部四半胱氨酸结构域的 Cx43 的同步细胞进行了光学脉冲追踪标记和单标记延时成像。在晚期有丝分裂中,较老的 Cx43 主要分离到质膜,而较新的 Cx43 则位于细胞内。这个较老的群体核化新的缝隙连接,允许有丝分裂退出后迅速恢复通讯。

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