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EphB-ephrinB双向内吞作用终止黏附,从而允许接触介导的排斥反应。

EphB-ephrinB bi-directional endocytosis terminates adhesion allowing contact mediated repulsion.

作者信息

Zimmer Manuel, Palmer Amparo, Köhler Jenny, Klein Rüdiger

机构信息

Max-Planck Institute of Neurobiology, Am Klopferspitz 18A, D-82152 Martinsried, Germany.

出版信息

Nat Cell Biol. 2003 Oct;5(10):869-78. doi: 10.1038/ncb1045. Epub 2003 Sep 14.

Abstract

Eph receptors and their membrane-associated ephrin ligands mediate cell-cell repulsion to guide migrating cells and axons. Repulsion requires that the ligand-receptor complex be removed from the cell surface, for example by proteolytic processing of the ephrin ectodomain. Here we show that cell contact-induced EphB-ephrinB complexes are rapidly endocytosed during the retraction of cells and neuronal growth cones. Endocytosis occurs in a bi-directional manner that comprises of full-length receptor and ligand complexes. Endocytosis is sufficient to promote cell detachment and seems necessary for axon withdrawal during growth cone collapse. Here, we show a mechanism for the termination of adhesion and the promotion of cell repulsion after intercellular (trans) interaction between two transmembrane proteins.

摘要

Eph受体及其膜相关的ephrin配体介导细胞间排斥,以引导迁移细胞和轴突。排斥作用要求配体-受体复合物从细胞表面移除,例如通过对ephrin胞外域进行蛋白水解处理。我们在此表明,细胞接触诱导的EphB-ephrinB复合物在细胞和神经元生长锥回缩过程中迅速被内吞。内吞以双向方式发生,包括全长受体和配体复合物。内吞足以促进细胞脱离,并且似乎是生长锥塌陷期间轴突回缩所必需的。在此,我们展示了一种在两个跨膜蛋白之间进行细胞间(反式)相互作用后终止黏附并促进细胞排斥的机制。

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