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Cdc42 is not essential for filopodium formation, directed migration, cell polarization, and mitosis in fibroblastoid cells
被引:134
作者:
Czuchra, A
Wu, XW
Meyer, H
van Hengel, J
Schroeder, T
Geffers, R
Rottner, K
Brakebusch, C
[1
]
机构:
[1] Max Planck Inst Biochem, Heisenberg Grp Regulat Cytoskeletal Org, D-82152 Martinsried, Germany
[2] Ghent Univ VIB, Dept Mol Biomed Res, Mol Cell Biol Unit, B-9000 Ghent, Belgium
[3] GSF Natl Res Ctr Environm & Hlth, Inst Stem Cell Res, D-85764 Neuherberg, Germany
[4] German Res Ctr Biotechnol, Mucosal Immun Grp, D-38124 Braunschweig, Germany
[5] German Res Ctr Biotechnol, Cytoskeleton Dynam Grp, D-38124 Braunschweig, Germany
关键词:
D O I:
10.1091/mbc.E05-01-0061
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
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.
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页码:4473 / 4484
页数:12
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