Morphogenesis of epithelial tubes: Insights into tube formation, elongation, and elaboration

被引:254
作者
Andrew, Deborah J. [1 ,2 ]
Ewald, Andrew J. [1 ,2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Cell Biol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Ctr Cell Dynam, Baltimore, MD 21205 USA
关键词
Apical constriction; Migration; Epithelia; Mesenchyme; Cancer; Apicobasal polarity; Branching morphogenesis; PLANAR-CELL-POLARITY; MAMMARY-GLAND DEVELOPMENT; FGF RECEPTOR HOMOLOG; TERMINAL END BUDS; BRANCHING MORPHOGENESIS; LUMEN FORMATION; URETERAL BUD; SALIVARY-GLAND; CONVERGENT EXTENSION; SECONDARY NEURULATION;
D O I
10.1016/j.ydbio.2009.09.024
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Epithelial tubes are a fundamental tissue across the metazoan phyla and provide an essential functional component of many of the major organs. Recent work in flies and mammals has begun to elucidate the cellular mechanisms driving the formation, elongation, and branching morphogenesis of epithelial tubes during development. Both forward and reverse genetic techniques have begun to identify critical molecular regulators for these processes and have revealed the conserved role of key pathways in regulating the growth and elaboration of tubular networks. In this review, we discuss the developmental programs driving the formation of branched epithelial networks, with specific emphasis on the trachea and salivary gland of Drosophila melanogaster and the mammalian lung, mammary gland, kidney, and salivary gland. We both highlight similarities in the development of these organs and attempt to identify tissue and organism specific strategies. Finally, we briefly consider how our understanding of the regulation of proliferation, apicobasal polarity, and epithelial motility during branching morphogenesis can be applied to understand the pathologic dysregulation of these same processes during metastatic cancer progression. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:34 / 55
页数:22
相关论文
共 214 条
[1]   Fork head and Sage maintain a uniform and patent salivary gland lumen through regulation of two downstream target genes, PH4αSG1 and PH4αSG2 [J].
Abrams, Elliott W. ;
Mihoulides, Whitney K. ;
Andrew, Deborah J. .
DEVELOPMENT, 2006, 133 (18) :3517-3527
[2]   Planar signaling and morphogenesis in Drosophila [J].
Adler, PN .
DEVELOPMENTAL CELL, 2002, 2 (05) :525-535
[3]   Coordinating cell fate and morphogenesis in Drosophila renal tubules [J].
Ainsworth, C ;
Wan, S ;
Skaer, H .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 2000, 355 (1399) :931-937
[4]   mummy/cystic encodes an enzyme required for chitin and glycan synthesis, involved in trachea, embryonic cuticle and CNS development -: Analysis of its role in Drosophila tracheal morphogenesis [J].
Araújo, SJ ;
Aslam, H ;
Tear, G ;
Casanova, J .
DEVELOPMENTAL BIOLOGY, 2005, 288 (01) :179-193
[5]   Genetic control of single lumen formation in the zebrafish gut [J].
Bagnat, Michel ;
Cheung, Isla D. ;
Mostov, Keith E. ;
Stainier, Didier Y. R. .
NATURE CELL BIOLOGY, 2007, 9 (08) :954-U119
[6]   The rho GTPase and a putative RhoGEF mediate a signaling pathway for the cell shape changes in Drosophila gastrulation [J].
Barrett, K ;
Leptin, M ;
Settleman, J .
CELL, 1997, 91 (07) :905-915
[7]   The planar polarity pathway promotes coordinated cell migration during Drosophila oogenesis [J].
Bastock, Rebecca ;
Strutt, David .
DEVELOPMENT, 2007, 134 (17) :3055-3064
[8]   RGD-dependent vacuolation and lumen formation observed during endothelial cell morphogenesis in three-dimensional fibrin matrices involves the αvβ3 and α5β1 integrins [J].
Bayless, KJ ;
Salazar, R ;
Davis, GE .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (05) :1673-1683
[9]  
Bayless KJ, 2002, J CELL SCI, V115, P1123
[10]   Vascular development: Cellular and molecular regulation [J].
Beck, L ;
DAmore, PA .
FASEB JOURNAL, 1997, 11 (05) :365-373