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三种机制控制E-钙黏蛋白定位于黏着小带。

Three mechanisms control E-cadherin localization to the zonula adherens.

作者信息

Woichansky Innokenty, Beretta Carlo Antonio, Berns Nicola, Riechmann Veit

机构信息

Department of Cell and Molecular Biology and Division of Signaling and Functional Genomics at the German Cancer Research Center (DKFZ), Medical Faculty Mannheim, Heidelberg University, Ludolf-Krehl-Strasse 13-17, D-68167 Mannheim, Germany.

Heidelberg University, COS and Nikon Imaging Center at the University of Heidelberg, Bioquant, D-69120 Heidelberg, Germany.

出版信息

Nat Commun. 2016 Mar 10;7:10834. doi: 10.1038/ncomms10834.

Abstract

E-cadherin localization to the zonula adherens is fundamental for epithelial differentiation but the mechanisms controlling localization are unclear. Using the Drosophila follicular epithelium we genetically dissect E-cadherin transport in an in vivo model. We distinguish three mechanisms mediating E-cadherin accumulation at the zonula adherens. Two membrane trafficking pathways deliver newly synthesized E-cadherin to the plasma membrane. One is Rab11 dependent and targets E-cadherin directly to the zonula adherens, while the other transports E-cadherin to the lateral membrane. Lateral E-cadherin reaches the zonula adherens by endocytosis and targeted recycling. We show that this pathway is dependent on RabX1, which provides a functional link between early and recycling endosomes. Moreover, we show that lateral E-cadherin is transported to the zonula adherens by an apically directed flow within the plasma membrane. Differential activation of these pathways could facilitate cell shape changes during morphogenesis, while their misregulation compromises cell adhesion and tissue architecture in differentiated epithelia.

摘要

E-钙黏蛋白定位于黏着小带对于上皮分化至关重要,但控制其定位的机制尚不清楚。利用果蝇卵泡上皮,我们在体内模型中对E-钙黏蛋白的转运进行了遗传学剖析。我们区分出三种介导E-钙黏蛋白在黏着小带积累的机制。两条膜运输途径将新合成的E-钙黏蛋白输送到质膜。一条途径依赖Rab11,直接将E-钙黏蛋白靶向运输到黏着小带,而另一条途径则将E-钙黏蛋白运输到侧膜。侧膜上的E-钙黏蛋白通过内吞作用和靶向再循环到达黏着小带。我们发现这条途径依赖RabX1,它在早期内体和再循环内体之间提供了功能联系。此外,我们还表明,侧膜上的E-钙黏蛋白通过质膜内的顶端定向流动被运输到黏着小带。这些途径的差异激活可能有助于形态发生过程中的细胞形状变化,而它们的失调则会损害分化上皮中的细胞黏附和组织结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c140/4792928/bc8db8690dc9/ncomms10834-f1.jpg

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