Molecular Regulation of Lumen Morphogenesis

被引:193
作者
Datta, Anirban [1 ]
Bryant, David M. [1 ]
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
关键词
MITOTIC SPINDLE ORIENTATION; EPITHELIAL-CELL POLARITY; LIPID PHOSPHATASE PTEN; PLASMA-MEMBRANE; TRANSCRIPTION FACTOR; TUBE ELONGATION; APICAL SURFACE; VESICLE TRAFFICKING; TIGHT JUNCTIONS; GENETIC-CONTROL;
D O I
10.1016/j.cub.2010.12.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The asymmetric polarization of cells allows specialized functions to be performed at discrete subcellular locales. Spatiotemporal coordination of polarization between groups of cells allowed the evolution of metazoa. For instance, coordinated apical-basal polarization of epithelial and endothelial cells allows transport of nutrients and metabolites across cell barriers and tissue microenvironments. The defining feature of such tissues is the presence of a central, interconnected lumina! network. Although tubular networks are present in seemingly different organ systems, such as the kidney, lung, and blood vessels, common underlying principles govern their formation. Recent studies using in vivo and in vitro models of lumen formation have shed new light on the molecular networks regulating this fundamental process. We here discuss progress in understanding common design principles underpinning de novo lumen formation and expansion.
引用
收藏
页码:R126 / R136
页数:11
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