The MRL proteins: Adapting cell adhesion, migration and growth

被引:29
作者
Colo, Georgina P. [1 ]
Lafuente, Esther M. [2 ]
Teixido, Joaquin [1 ]
机构
[1] CSIC, Ctr Invest Biol, Dept Cellular & Mol Med, Madrid 28040, Spain
[2] Univ Complutense Madrid, Fac Med, Dept Microbiol 1, E-28040 Madrid, Spain
基金
欧盟第七框架计划;
关键词
MRL family; RIAM; Lamellipodin; MIG-10; Pico; C-ELEGANS CELL; ACTIN CYTOSKELETON; AXON GUIDANCE; INTEGRIN ALPHA-IIB-BETA-3; T-CELLS; ACTIVATION; RIAM; LAMELLIPODIN; OUTGROWTH; INTERACTS;
D O I
10.1016/j.ejcb.2012.03.001
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
MIG-10, RIAM and Lamellipodin (Lpd) are the founding members of the MRI. family of multi-adaptor molecules. These proteins have common domain structures but display distinct functions in cell migration and adhesion, signaling, and in cell growth. The binding of RIAM with active Rap1 and with talin provides these MRL molecules with important regulatory roles on integrin-mediated cell adhesion and migration. Furthermore, RIAM and Lpd can regulate actin dynamics through their binding to actin regulatory Ena/VASP proteins. Recent data generated with the Drosophila MRL ortholog called Pico and with RIAM in melanoma cells indicate that these proteins can also regulate cell growth. As MRL proteins represent a relatively new family, many questions on their structure-function relationships remain unanswered, including regulation of their expression, post-translational modifications, new interactions, involvement in signaling and their knockout mice phenotype. (C) 2012 Elsevier GmbH. All rights reserved.
引用
收藏
页码:861 / 868
页数:8
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