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Rac-PAK信号传导通过调节MEK1-ERK复合物的形成来刺激细胞外信号调节激酶(ERK)的激活。

Rac-PAK signaling stimulates extracellular signal-regulated kinase (ERK) activation by regulating formation of MEK1-ERK complexes.

作者信息

Eblen Scott T, Slack Jill K, Weber Michael J, Catling Andrew D

机构信息

Department of Microbiology, School of Medicine, University of Virginia, Charlottesville, Virginia 22908, USA.

出版信息

Mol Cell Biol. 2002 Sep;22(17):6023-33. doi: 10.1128/MCB.22.17.6023-6033.2002.

Abstract

Utilizing mutants of extracellular signal-regulated kinase 2 (ERK2) that are defective for intrinsic mitogen-activated protein kinase or ERK kinase (MEK) binding, we have identified a convergent signaling pathway that facilitates regulated MEK-ERK association and ERK activation. ERK2-delta19-25 mutants defective in MEK binding could be phosphorylated in response to mitogens; however, signaling from the Raf-MEK pathway alone was insufficient to stimulate their phosphorylation in COS-1 cells. Phosphorylation of ERK2-delta19-25 but not of wild-type ERK2 in response to Ras V12 was greatly inhibited by dominant-negative Rac. Activated forms of Rac and Cdc42 could enhance the association of wild-type ERK2 with MEK1 but not with MEK2 in serum-starved adherent cells. This effect was p21-activated kinase (PAK) dependent and required the putative PAK phosphorylation sites T292 and S298 of MEK1. In detached cells placed in suspension, ERK2 was complexed with MEK2 but not with MEK1. However, upon replating of cells onto a fibronectin matrix, there was a substantial induction of MEK1-ERK2 association and ERK activation, both of which could be inhibited by dominant-negative PAK1. These data show that Rac facilitates the assembly of a mitogen-activated protein kinase signaling complex required for ERK activation and that this facilitative signaling pathway is active during adhesion to the extracellular matrix. These findings reveal a novel mechanism by which adhesion and growth factor signals are integrated during ERK activation.

摘要

利用对内在丝裂原活化蛋白激酶或细胞外信号调节激酶激酶(MEK)结合有缺陷的细胞外信号调节激酶2(ERK2)突变体,我们确定了一条汇聚信号通路,该通路促进了受调控的MEK-ERK结合和ERK激活。在MEK结合方面存在缺陷的ERK2-δ19-25突变体可响应丝裂原而被磷酸化;然而,仅Raf-MEK通路发出的信号不足以刺激其在COS-1细胞中的磷酸化。显性负性Rac可极大地抑制ERK2-δ19-25而非野生型ERK2对Ras V12的响应磷酸化。在血清饥饿的贴壁细胞中,Rac和Cdc42的活化形式可增强野生型ERK2与MEK1的结合,但不能增强与MEK2的结合。这种效应依赖于p21活化激酶(PAK),且需要MEK1的假定PAK磷酸化位点T292和S298。在置于悬浮液中的脱离细胞中,ERK2与MEK2形成复合物,而不与MEK1形成复合物。然而,当细胞重新接种到纤连蛋白基质上时,MEK1-ERK2结合和ERK激活会大量诱导,这两者均可被显性负性PAK1抑制。这些数据表明,Rac促进了ERK激活所需的丝裂原活化蛋白激酶信号复合物的组装,且这种促进性信号通路在细胞黏附于细胞外基质过程中是活跃的。这些发现揭示了一种在ERK激活过程中整合黏附信号和生长因子信号的新机制。

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