Concepts and consequences of Eph receptor clustering

被引:86
作者
Janes, Peter W. [1 ]
Nievergall, Eva [1 ]
Lackmann, Martin [1 ]
机构
[1] Monash Univ, Dept Biochem & Mol Biol, Clayton, Vic 3800, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Eph receptors; Ephrins; Eph oligomerisation; Homotypic Eph-Eph clusters; Heterotypic EphA-EphB clusters; COLORECTAL-CANCER PROGRESSION; TYROSINE KINASE; TRANSMEMBRANE DOMAIN; CELL-MIGRATION; E-CADHERIN; SOMATIC MUTATIONS; SIGNALING PATHWAY; CRYSTAL-STRUCTURE; PROSTATE-CANCER; LIGAND-BINDING;
D O I
10.1016/j.semcdb.2012.01.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Polymeric receptor-ligand complexes between interacting Eph and ephrin-expressing cells are regarded as dynamic intercellular signalling scaffolds that control cell-to-cell contact: the resulting Eph-ephrin signalling clusters function as positional cues that facilitate cell navigation and tissue patterning during normal and oncogenic development. The considerable complexity of this task, coordinating a multitude of cell movements and cellular interactions, is achieved by accurate translation of spatial information from Eph and ephrin expression gradients into fine-tuned changes in cell-cell adhesion and position. Here we review emerging evidence suggesting that the required combinatorial diversity is not only achieved by the large number of possible Eph-ephrin interactions and selective use of Eph forward and ephrin reverse signals, but in particular through the composition and signal capacity of Eph-ephrin clusters, which is adjusted dynamically to reflect overall Eph and ephrin surface densities on interacting cells. Fine-tuning is provided through multi-layered cluster assembly, where homo-and heterotypic Eph and ephrin interactions define the composition - whilst intracellular signalling feedbacks determine the size and lifetime - of signalling clusters. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:43 / 50
页数:8
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