Department of Cell and Developmental Biology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA.
Nat Cell Biol. 2011 Jun;13(6):722-7. doi: 10.1038/ncb2254. Epub 2011 May 15.
How individual cells respond to mechanical forces is of considerable interest to biologists as force affects many aspects of cell behaviour. The application of force on integrins triggers cytoskeletal rearrangements and growth of the associated adhesion complex, resulting in increased cellular stiffness, also known as reinforcement. Although RhoA has been shown to play a role during reinforcement, the molecular mechanisms that regulate its activity are unknown. By combining biochemical and biophysical approaches, we identified two guanine nucleotide exchange factors (GEFs), LARG and GEF-H1, as key molecules that regulate the cellular adaptation to force. We show that stimulation of integrins with tensional force triggers activation of these two GEFs and their recruitment to adhesion complexes. Surprisingly, activation of LARG and GEF-H1 involves distinct signalling pathways. Our results reveal that LARG is activated by the Src family tyrosine kinase Fyn, whereas GEF-H1 catalytic activity is enhanced by ERK downstream of a signalling cascade that includes FAK and Ras.
细胞如何对机械力做出反应是生物学家非常感兴趣的问题,因为力会影响细胞行为的许多方面。整合素受到力的作用会触发细胞骨架的重新排列和相关黏附复合物的生长,从而导致细胞硬度增加,也就是所谓的加固。尽管已经表明 RhoA 在加固过程中发挥作用,但调节其活性的分子机制尚不清楚。通过结合生化和生物物理方法,我们确定了两个鸟嘌呤核苷酸交换因子(GEF),LARG 和 GEF-H1,作为调节细胞适应力的关键分子。我们表明,张力刺激整合素会触发这两个 GEF 的激活及其向黏附复合物的募集。令人惊讶的是,LARG 和 GEF-H1 的激活涉及不同的信号通路。我们的结果表明,LARG 被Src 家族酪氨酸激酶 Fyn 激活,而 GEF-H1 的催化活性则通过包括 FAK 和 Ras 的信号级联的下游 ERK 增强。