The Cdc42 GEF Intersectin 2 controls mitotic spindle orientation to form the lumen during epithelial morphogenesis

被引:102
作者
Rodriguez-Fraticelli, Alejo E. [1 ]
Vergarajauregui, Silvia [1 ]
Eastburn, Dennis J. [2 ]
Datta, Anirban [2 ]
Alonso, Miguel A. [1 ]
Mostov, Keith [2 ]
Martin-Belmonte, Fernando [1 ]
机构
[1] CSIC, Ctr Biol Mol Severo Ochoa, E-28049 Madrid, Spain
[2] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
PLASMA-MEMBRANE; CELL-POLARITY; APICAL-POLARITY; SMALL GTPASES; RHO-GTPASES; MDCK CELLS; PROTEIN; ENDOCYTOSIS; EXOCYTOSIS; CENTROSOMES;
D O I
10.1083/jcb.201002047
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Epithelial organs are made of tubes and cavities lined by a monolayer of polarized cells that enclose the central lumen. Lumen formation is a crucial step in the formation of epithelial organs. The Rho guanosine triphosphatase (GTPase) Cdc42, which is a master regulator of cell polarity, regulates the formation of the central lumen in epithelial morphogenesis. However, how Cdc42 is regulated during this process is still poorly understood. Guanine nucleotide exchange factors (GEFs) control the activation of small GTPases. Using the three-dimensional Madin-Darby canine kidney model, we have identified a Cdc42-specific GEF, Intersectin 2 (ITSN2), which localizes to the centro-somes and regulates Cdc42 activation during epithelial morphogenesis. Silencing of either Cdc42 or ITSN2 disrupts the correct orientation of the mitotic spindle and normal lumen formation, suggesting a direct relationship between these processes. Furthermore, we demonstrated this direct relationship using LGN, a component of the machinery for mitotic spindle positioning, whose disruption also results in lumen formation defects.
引用
收藏
页码:725 / 738
页数:14
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