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Rac依赖的ephrinBs反式内吞作用调节Eph-ephrin接触排斥。

Rac-dependent trans-endocytosis of ephrinBs regulates Eph-ephrin contact repulsion.

作者信息

Marston Daniel J, Dickinson Sarah, Nobes Catherine D

机构信息

Centre for Cell and Molecular Dynamics, Department of Anatomy and Developmental Biology, University College London, UK.

出版信息

Nat Cell Biol. 2003 Oct;5(10):879-88. doi: 10.1038/ncb1044. Epub 2003 Sep 14.

Abstract

Eph receptor-ephrin signals are important for controlling repulsive and attractive cell movements during tissue patterning in embryonic development. However, the dynamic cellular responses to these signals at cell-cell contact sites are poorly understood. To examine these events we have used cell microinjection to express EphB4 and ephrinB2 in adjacent Swiss 3T3 fibroblasts and have studied the interaction of the injected cells using time-lapse microscopy. We show that Eph receptors are locally activated wherever neighbouring cells make contact. This triggers dynamic, Rac-regulated membrane ruffles at the Eph-ephrin contact sites. Subsequently, the receptor and ligand cells retract from one another, concomitantly with the endocytosis of the activated Eph receptors and their bound, full-length ephrinB ligands. Both the internalization of the receptor-ligand complexes and the subsequent cell retraction events are dependent on actin polymerization, which in turn is dependent on Rac signalling within the receptor-expressing cells. Similar events occur in primary human endothelial cells. Our findings suggest a novel mechanism for cell repulsion, in which the contact between Eph-expressing and ephrin-expressing cells is destabilized by the localized phagocytosis of the ligand-expressing cell plasma membrane by the receptor-expressing cell.

摘要

在胚胎发育过程中的组织模式形成期间,Eph受体 - 促红细胞生成素受体相互作用蛋白(ephrin)信号对于控制排斥性和吸引性细胞运动很重要。然而,在细胞 - 细胞接触位点对这些信号的动态细胞反应却知之甚少。为了研究这些事件,我们利用细胞显微注射技术在相邻的瑞士3T3成纤维细胞中表达EphB4和ephrinB2,并使用延时显微镜研究注射细胞之间的相互作用。我们发现,只要相邻细胞发生接触,Eph受体就会在局部被激活。这会在Eph - ephrin接触位点触发由Rac调节的动态膜褶皱。随后,受体细胞和配体细胞相互回缩,同时激活的Eph受体及其结合的全长ephrinB配体发生内吞作用。受体 - 配体复合物的内化以及随后的细胞回缩事件都依赖于肌动蛋白聚合,而肌动蛋白聚合又依赖于表达受体的细胞内的Rac信号传导。在原代人内皮细胞中也会发生类似事件。我们的研究结果提示了一种新的细胞排斥机制,即表达Eph的细胞与表达ephrin的细胞之间通过表达受体的细胞对表达配体的细胞质膜进行局部吞噬作用而使接触不稳定。

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