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[已解决求助] development [复制链接]

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金话筒 优秀版主 优秀会员 积极份子 帅哥研究员 小小研究员

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发表于 2011-3-2 14:44 |只看该作者 |倒序浏览 |打印
http://www.ncbi.nlm.nih.gov/pubmed/21098570
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Development. 2010 Dec;137(24):4295-305.4 w: m  d! Y8 W8 T% g

  H' t$ D9 \2 a& A- oEpithelial dynamics of pancreatic branching morphogenesis.$ _: {# |8 ?1 `3 @/ h/ q$ t6 [, m, }
Villasenor A, Chong DC, Henkemeyer M, Cleaver O.
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Department of Molecular Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA.
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Abstract8 P1 e/ f7 ?( b' X; W0 G
The mammalian pancreas is a highly branched gland, essential for both digestion and glucose homeostasis. Pancreatic branching, however, is poorly understood, both at the ultrastructural and cellular levels. In this article, we characterize the morphogenesis of pancreatic branches, from gross anatomy to the dynamics of their epithelial organization. We identify trends in pancreatic branch morphology and introduce a novel mechanism for branch formation, which involves transient epithelial stratification and partial loss of cell polarity, changes in cell shape and cell rearrangements, de novo tubulogenesis and epithelial tubule remodeling. In contrast to the classical epithelial budding and tube extension observed in other organs, a pancreatic branch takes shape as a multi-lumen tubular plexus coordinately extends and remodels into a ramifying, single-lumen ductal system. Moreover, our studies identify a role for EphB signaling in epithelial remodeling during pancreatic branching. Overall, these results illustrate distinct, step-wise cellular mechanisms by which pancreatic epithelium shapes itself to create a functional branching organ.
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$ S( o- l. \+ L9 c( F" D  WPMID: 21098570 [PubMed - indexed for MEDLINE]PMCID: PMC2990215 [Available on 2011/12/15]

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发表于 2011-3-3 00:04 |只看该作者
Development. 2010 Dec;137(24):4295-305.
1 j! N8 A8 z( X( y# [: H4 m4 BEpithelial dynamics of pancreatic branching morphogenesis.% R8 _; M, `/ g& l! t' G
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Villasenor A, Chong DC, Henkemeyer M, Cleaver O.* t& ^4 U& L% {; s6 t

+ Y2 t0 M( `; r% kDepartment of Molecular Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA.
, ~' w, y7 ^8 r) E. t2 X! k% CAbstract
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1 P; p- `  V# ~The mammalian pancreas is a highly branched gland, essential for both digestion and glucose homeostasis. Pancreatic branching, however, is poorly understood, both at the ultrastructural and cellular levels. In this article, we characterize the morphogenesis of pancreatic branches, from gross anatomy to the dynamics of their epithelial organization. We identify trends in pancreatic branch morphology and introduce a novel mechanism for branch formation, which involves transient epithelial stratification and partial loss of cell polarity, changes in cell shape and cell rearrangements, de novo tubulogenesis and epithelial tubule remodeling. In contrast to the classical epithelial budding and tube extension observed in other organs, a pancreatic branch takes shape as a multi-lumen tubular plexus coordinately extends and remodels into a ramifying, single-lumen ductal system. Moreover, our studies identify a role for EphB signaling in epithelial remodeling during pancreatic branching. Overall, these results illustrate distinct, step-wise cellular mechanisms by which pancreatic epithelium shapes itself to create a functional branching organ.
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