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粘着斑激酶信号出现在意想不到的位置。

Focal adhesion kinase signaling in unexpected places.

作者信息

Kleinschmidt Elizabeth G, Schlaepfer David D

机构信息

Biomedical Sciences Graduate Program, University of California, San Diego, CA, United States; Moores Cancer Center, Department of Reproductive Medicine, 3855 Health Sciences Drive, MC 0983, La Jolla, CA 92093-0983, United States.

Biomedical Sciences Graduate Program, University of California, San Diego, CA, United States; Moores Cancer Center, Department of Reproductive Medicine, 3855 Health Sciences Drive, MC 0983, La Jolla, CA 92093-0983, United States.

出版信息

Curr Opin Cell Biol. 2017 Apr;45:24-30. doi: 10.1016/j.ceb.2017.01.003. Epub 2017 Feb 16.

Abstract

Focal adhesion kinase (FAK) is a cytoplasmic protein-tyrosine kinase first identified at extracellular matrix and integrin receptor cell adhesion sites and is a key regulator of cell movement. FAK is activated by a variety of stimuli. Herein, we discuss advances in conformational-associated FAK activation and dimerization mechanisms. Additionally, new roles have emerged for FAK signaling at cell adhesions, adherens junctions, endosomes, and the nucleus. In light of these new findings, we review how FAK activation at these sites is connected to the regulation of integrin recycling-activation, vascular permeability, cell survival, and transcriptional regulation, respectively. Studies uncovering FAK signaling connections in unexpected places within cells have yielded important new regulatory insights in cell biology.

摘要

粘着斑激酶(FAK)是一种细胞质蛋白酪氨酸激酶,最初在细胞外基质和整合素受体细胞粘附位点被发现,是细胞运动的关键调节因子。FAK可被多种刺激激活。在此,我们讨论与构象相关的FAK激活和二聚化机制的进展。此外,FAK信号在细胞粘附、黏着连接、内体和细胞核中也出现了新的作用。鉴于这些新发现,我们分别综述了这些位点的FAK激活如何与整合素循环激活、血管通透性、细胞存活和转录调控的调节相关联。在细胞内意外位置发现FAK信号连接的研究在细胞生物学中产生了重要的新调节见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9ca/5482783/147da76fe8e9/nihms849756f1.jpg

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