Chen Q, Kinch M S, Lin T H, Burridge K, Juliano R L
Department of Pharmacology, School of Medicine, University of North Carolina, Chapel Hill 27599.
J Biol Chem. 1994 Oct 28;269(43):26602-5.
Integrins can function as signal-transducing receptors capable of modulating cell growth and gene expression (Juliano, R. L., and Haskill, S. (1993) J. Cell Biol. 120, 577-585; Hynes, R. O. (1992) Cell 69, 11-25). An early event in integrin signaling in fibroblasts and other cells involves activation of pp125FAK, a cytoplasmic tyrosine kinase (Hanks, S. K., Calalb, M. B., Harper, M. C., and Patel, S. K. (1992) Proc. Natl. Acad. Sci. U. S. A. 89, 8487-8491; Schaller, M. D., Borgman, C. A., Cobb, B. S., Vines, R. R., Reynolds, A. B., and Parsons, J. T. (1992) Proc. Natl. Acad. Sci. U. S. A. 89, 5192-5196). Here we report a novel aspect of integrin-mediated signal transduction. We demonstrate that adhesion of cells to substrata coated with extracellular matrix proteins, or with a synthetic peptide containing the RGD sequence, can cause activation of mitogen-activated protein (MAP) kinases in 3T3 or REF52 fibroblasts. Activation of MAP kinases seems to depend on integrin engagement rather than simply on cell attachment. Thus, MAP kinases are activated when cells adhere to substrata coated with the integrin ligands fibronectin or laminin, but not when cells adhere to poly-D-lysine, a nonspecific adhesion-promoting polypeptide. Treatment of cells with cytochalasin D, an inhibitor of actin microfilament assembly, almost completely blocks adhesion-induced MAP kinase activation, indicating a critical role for the cytoskeleton. In REF52 cells, we have observed that activation of MAP kinases is accompanied by redistribution of the protein to the nucleus, suggesting that the activated kinases may impinge on factors regulating gene expression. Thus, integrin-mediated cell adhesion seems a sufficient stimulus to cause activation and nuclear translocation of MAP kinases. This may have important implications for the regulation of cell growth and differentiation by the extracellular matrix.
整合素可作为能够调节细胞生长和基因表达的信号转导受体(朱利亚诺,R.L.,和哈斯基尔,S.(1993年)《细胞生物学杂志》120卷,577 - 585页;海因斯,R.O.(1992年)《细胞》69卷,11 - 25页)。成纤维细胞和其他细胞中整合素信号传导的早期事件涉及pp125FAK(一种细胞质酪氨酸激酶)的激活(汉克斯,S.K.,卡拉尔布,M.B.,哈珀,M.C.,和帕特尔,S.K.(1992年)《美国国家科学院院刊》89卷,8487 - 8491页;沙勒,M.D.,博格曼,C.A.,科布,B.S.,瓦因斯,R.R.,雷诺兹,A.B.,和帕森斯J.T.(1992年)《美国国家科学院院刊》89卷,5192 - 5196页)。在此我们报道整合素介导的信号转导的一个新方面。我们证明细胞与包被有细胞外基质蛋白或含有RGD序列的合成肽的基质黏附,可在3T3或REF52成纤维细胞中引起丝裂原活化蛋白(MAP)激酶的激活。MAP激酶的激活似乎依赖于整合素的结合,而不仅仅是细胞附着。因此,当细胞黏附到包被有整合素配体纤连蛋白或层粘连蛋白的基质上时,MAP激酶被激活,但当细胞黏附到聚-D-赖氨酸(一种非特异性促黏附多肽)上时则不然。用细胞松弛素D(一种肌动蛋白微丝组装抑制剂)处理细胞,几乎完全阻断黏附诱导的MAP激酶激活,表明细胞骨架起关键作用。在REF52细胞中,我们观察到MAP激酶的激活伴随着该蛋白向细胞核的重新分布,这表明活化的激酶可能影响调节基因表达的因子。因此,整合素介导的细胞黏附似乎是导致MAP激酶激活和核转位的充分刺激。这可能对细胞外基质对细胞生长和分化的调节具有重要意义。