A molecular network for de novo generation of the apical surface and lumen

被引:447
作者
Bryant, David M. [1 ]
Datta, Anirban [1 ]
Rodriguez-Fraticelli, Alejo E. [3 ]
Peranen, Johan [4 ]
Martin-Belmonte, Fernando [3 ]
Mostov, Keith E. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
[3] CSIC, Ctr Biol Mol Severo Ochoa, E-28049 Madrid, Spain
[4] Univ Helsinki, Inst Biotechnol, FIN-00014 Helsinki, Finland
关键词
MITOTIC SPINDLE ORIENTATION; POLARIZED EPITHELIAL-CELLS; MDCK CELLS; PRIMARY CILIOGENESIS; EXCHANGE FACTOR; PRIMARY CILIUM; RAB GTPASES; CDC42; GEF; MORPHOGENESIS; TRAFFICKING;
D O I
10.1038/ncb2106
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To form epithelial organs cells must polarize and generate de novo an apical domain and lumen. Epithelial polarization is regulated by polarity complexes that are hypothesized to direct downstream events, such as polarized membrane traffic, although this interconnection is not well understood. We have found that Rab11a regulates apical traffic and lumen formation through the Rab guanine nucleotide exchange factor (GEF), Rabin8, and its target, Rab8a. Rab8a and Rab11a function through the exocyst to target Par3 to the apical surface, and control apical Cdc42 activation through the Cdc42 GEF, Tuba. These components assemble at a transient apical membrane initiation site to form the lumen. This Rab11a-directed network directs Cdc42-dependent apical exocytosis during lumen formation, revealing an interaction between the machineries of vesicular transport and polarization.
引用
收藏
页码:1035 / U24
页数:23
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