共 40 条
Hold on tightly How to keep the local activation of small GTPases
被引:7
作者:
Garcia-Cattaneo, Alejandra
[1
]
Braga, Vania M. M.
[1
]
机构:
[1] Univ London Imperial Coll Sci Technol & Med, Fac Med, Natl Heart & Lung Inst, London, England
基金:
英国医学研究理事会;
关键词:
cell-cell adhesion;
Rho GTPases;
Ajuba;
cytoskeletal proteins;
cell migration;
activation signaling;
affinity regulation;
post-translation modifications;
CELL-CELL ADHESION;
LIM PROTEIN AJUBA;
CONTACT INHIBITION;
RAC ACTIVATION;
RHO;
IQGAP1;
JUNCTIONS;
BINDING;
DOMAIN;
PAK1;
D O I:
10.4161/cam.24646
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Signaling regulated by Rho small GTPases plays a pivotal role in cell migration, cell attachment to substratum or to their neighbors among other functions. Concerted efforts have focused on understanding how different GTPases are activated by specific stimuli and which regulator is responsible for the spatio-temporal control of their activity at particular intracellular sites. We have recently described the role of a scaffold protein, Ajuba, in adherens junction maintenance via direct stabilization of activated small GTPase Rac1 at cell-cell contacts. Ajuba binds to both active and inactive forms of Rac1. Upon junction formation, Rac1 activation initiates a positive feedback loop leading to Ajuba phosphorylation and Ajuba-mediated retention of activated Rac1 at junctions. Thus, cytoskeletal proteins may have a dual role to provide a scaffolding platform and dynamically modulate small GTPases function at a specific place, irrespective of their ability to interact with active and inactive forms. Here we discuss similar mechanisms via which cytoskeletal proteins can facilitate cellular processes downstream of Rho proteins by increasing their affinity to activated GTPases.
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页码:283 / 287
页数:5
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