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An Arf6-and caveolae-dependent pathway links hemidesmosome remodeling and mechanoresponse

机译:ARF6和Caveolae依赖性途径链接血液质膜重塑和力量

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摘要

Hemidesmosomes (HDs) are epithelial-specific cell-matrix adhesions that stably anchor the intracellular keratin network to the extracellular matrix. Although their main role is to protect the epithelial sheet from external mechanical strain, how HDs respond to mechanical stress remains poorly understood. Here we identify a pathway essential for HD remodeling and outline its role with respect to alpha 6 beta 4 integrin recycling. We find that alpha 6 beta 4 integrin chains localize to the plasma membrane, caveolae, and ADP-ribosylation factor-6+ (Arf6+) endocytic compartments. Based on fluorescence recovery after photobleaching and endocytosis assays, integrin recycling between both sites requires the small GTPase Arf6 but neither caveolin1 (Cav1) nor Cavin1. Strikingly, when keratinocytes are stretched or hypoosmotically shocked, alpha 6 beta 4 integrin accumulates at cell edges, whereas Cav1 disappears from it. This process, which is isotropic relative to the orientation of stretch, depends on Arf6, Cav1, and Cavin1. We propose that mechanically induced HD growth involves the isotropic flattening of caveolae (known for their mechanical buffering role) associated with integrin diffusion and turnover.
机译:Hemidemosomes(HDS)是上皮特异性细胞基质粘连,其稳定地将细胞内角蛋白网络锚定到细胞外基质。虽然它们的主要作用是保护上皮片免受外部机械菌株,但HDS如何应对机械应力仍然仍然清晰。在这里,我们鉴定了对HD重塑和概述其在α6β4整联蛋白回收的作用的途径。我们发现α6β4整合蛋白链定位于质膜,Caveolae和Adp-核糖基化因子-6 +(ARF6 +)内吞室。基于光漂白和内吞作用检测后的荧光回收,两种部位之间的整联素回收需要小GTP酶ARF6,但既不是Caveolin1(Cav1)也不是Cavin1。尖锐的是,当角质形成细胞被拉伸或低管震动时,α6β4整合蛋白在细胞边缘累积,而Cav1消失在其中。该过程是相对于拉伸方向的各向同性,取决于ARF6,Cav1和Cavin1。我们提出机械诱导的高清生长涉及Caveolae(已知为其机械缓冲作用)的各向同性平整,与整联蛋白扩散和转换相关。

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  • 来源
    《Molecular biology of the cell》 |2018年第4期|共17页
  • 作者单位

    INSERM CNRS IGBMC Dev &

    Stem Cells Program UMR 7104 U964 F-67400 Illkirch Graffenstaden France;

    INSERM CNRS IGBMC Dev &

    Stem Cells Program UMR 7104 U964 F-67400 Illkirch Graffenstaden France;

    INSERM CNRS IGBMC Dev &

    Stem Cells Program UMR 7104 U964 F-67400 Illkirch Graffenstaden France;

    MN3T U1109 INSERM F-67200 Strasbourg France;

    MN3T U1109 INSERM F-67200 Strasbourg France;

    INSERM CNRS IGBMC Dev &

    Stem Cells Program UMR 7104 U964 F-67400 Illkirch Graffenstaden France;

    INSERM CNRS IGBMC Dev &

    Stem Cells Program UMR 7104 U964 F-67400 Illkirch Graffenstaden France;

    INSERM CNRS IGBMC Dev &

    Stem Cells Program UMR 7104 U964 F-67400 Illkirch Graffenstaden France;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子生物学;
  • 关键词

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