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Cdc42对于成纤维样细胞中的丝状伪足形成、定向迁移、细胞极化和有丝分裂并非必不可少。

Cdc42 is not essential for filopodium formation, directed migration, cell polarization, and mitosis in fibroblastoid cells.

作者信息

Czuchra Aleksandra, Wu Xunwei, Meyer Hannelore, van Hengel Jolanda, Schroeder Timm, Geffers Robert, Rottner Klemens, Brakebusch Cord

机构信息

Heisenberg Group "Regulation of Cytoskeletal Organization," Max Planck Institute of Biochemistry, 82152 Martinsried, Germany.

出版信息

Mol Biol Cell. 2005 Oct;16(10):4473-84. doi: 10.1091/mbc.e05-01-0061. Epub 2005 Jul 12.

Abstract

Cdc42 is a small GTPase involved in the regulation of the cytoskeleton and cell polarity. To test whether Cdc42 has an essential role in the formation of filopodia or directed cell migration, we generated Cdc42-deficient fibroblastoid cells by conditional gene inactivation. We report here that loss of Cdc42 did not affect filopodium or lamellipodium formation and had no significant influence on the speed of directed migration nor on mitosis. Cdc42-deficient cells displayed a more elongated cell shape and had a reduced area. Furthermore, directionality during migration and reorientation of the Golgi apparatus into the direction of migration was decreased. However, expression of dominant negative Cdc42 in Cdc42-null cells resulted in strongly reduced directed migration, severely reduced single cell directionality, and complete loss of Golgi polarization and of directionality of protrusion formation toward the wound, as well as membrane blebbing. Thus, our data show that besides Cdc42 additional GTPases of the Rho-family, which share GEFs with Cdc42, are involved in the establishment and maintenance of cell polarity during directed migration.

摘要

Cdc42是一种小GTP酶,参与细胞骨架和细胞极性的调节。为了测试Cdc42在丝状伪足形成或定向细胞迁移中是否起关键作用,我们通过条件基因失活生成了Cdc42缺陷的成纤维样细胞。我们在此报告,Cdc42的缺失不影响丝状伪足或片状伪足的形成,对定向迁移速度或有丝分裂也无显著影响。Cdc42缺陷细胞呈现出更细长的细胞形态且面积减小。此外,迁移过程中的方向性以及高尔基体向迁移方向的重新定向均降低。然而,在Cdc42缺失细胞中表达显性负性Cdc42会导致定向迁移大幅减少、单细胞方向性严重降低、高尔基体极化以及向伤口方向的突起形成方向性完全丧失,同时伴有膜泡形成。因此,我们的数据表明,除了Cdc42之外,与Cdc42共享鸟嘌呤核苷酸交换因子(GEF)的Rho家族的其他GTP酶也参与定向迁移过程中细胞极性的建立和维持。

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