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磷酸肌醇3激酶C2β通过依赖Rac的机制调节细胞骨架组织和细胞迁移。

Phosphoinositide 3-Kinase C2beta regulates cytoskeletal organization and cell migration via Rac-dependent mechanisms.

作者信息

Katso Roy M, Pardo Olivier E, Palamidessi Andrea, Franz Clemens M, Marinov Marin, De Laurentiis Angela, Downward Julian, Scita Giorgio, Ridley Anne J, Waterfield Michael D, Arcaro Alexandre

机构信息

Ludwig Institute for Cancer Research, Royal Free and University College Hospital Medical School, London W1W 7BS, United Kingdom.

出版信息

Mol Biol Cell. 2006 Sep;17(9):3729-44. doi: 10.1091/mbc.e05-11-1083. Epub 2006 Jun 14.

Abstract

Receptor-linked class I phosphoinositide 3-kinases (PI3Ks) induce assembly of signal transduction complexes through protein-protein and protein-lipid interactions that mediate cell proliferation, survival, and migration. Although class II PI3Ks have the potential to make the same phosphoinositides as class I PI3Ks, their precise cellular role is currently unclear. In this report, we demonstrate that class II phosphoinositide 3-kinase C2beta (PI3KC2beta) associates with the Eps8/Abi1/Sos1 complex and is recruited to the EGF receptor as part of a multiprotein signaling complex also involving Shc and Grb2. Increased expression of PI3KC2beta stimulated Rac activity in A-431 epidermoid carcinoma cells, resulting in enhanced membrane ruffling and migration speed of the cells. Conversely, expression of dominant negative PI3KC2beta reduced Rac activity, membrane ruffling, and cell migration. Moreover, PI3KC2beta-overexpressing cells were protected from anoikis and displayed enhanced proliferation, independently of Rac function. Taken together, these findings suggest that PI3KC2beta regulates the migration and survival of human tumor cells by distinct molecular mechanisms.

摘要

受体连接的I类磷酸肌醇3激酶(PI3Ks)通过蛋白质 - 蛋白质和蛋白质 - 脂质相互作用诱导信号转导复合物的组装,这些相互作用介导细胞增殖、存活和迁移。虽然II类PI3Ks有可能产生与I类PI3Ks相同的磷酸肌醇,但它们确切的细胞作用目前尚不清楚。在本报告中,我们证明II类磷酸肌醇3激酶C2β(PI3KC2β)与Eps8/Abi1/Sos1复合物相关联,并作为多蛋白信号复合物的一部分被招募到表皮生长因子(EGF)受体,该复合物还涉及Shc和Grb2。PI3KC2β表达增加刺激了A - 431表皮样癌细胞中的Rac活性,导致细胞的膜皱褶和迁移速度增强。相反,显性负性PI3KC2β的表达降低了Rac活性、膜皱褶和细胞迁移。此外,过表达PI3KC2β的细胞对失巢凋亡具有抗性,并表现出增殖增强,这与Rac功能无关。综上所述,这些发现表明PI3KC2β通过不同的分子机制调节人类肿瘤细胞的迁移和存活。

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