Gdnf Is Mitogenic, Neurotrophic, and Chemoattractive to Enteric Neural Crest Cells in the Embryonic Colon

被引:37
作者
Mwizerwa, Olive [1 ,2 ]
Das, Pragnya [3 ]
Nagy, Nandor [4 ]
Akbareian, Sophia E. [1 ,2 ]
Mably, John D. [2 ,5 ]
Goldstein, Allan M. [1 ,2 ]
机构
[1] Massachusetts Gen Hosp, Dept Pediat Surg, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Childrens Hosp Philadelphia, Dept Pathol, Philadelphia, PA 19104 USA
[4] Semmelweis Univ, Fac Med, Dept Human Morphol & Dev Biol, Budapest, Hungary
[5] Childrens Hosp, Dept Pediat & Genet, Boston, MA 02115 USA
关键词
enteric nervous system; glial-derived neurotrophic factor; Gdnf; Ret; Hirschsprung's disease; chick; RECEPTOR TYROSINE KINASE; NERVOUS-SYSTEM; MICE LACKING; HIRSCHSPRUNGS-DISEASE; IN-VITRO; MIGRATION; NEURONS; RET; PROLIFERATION; GUT;
D O I
10.1002/dvdy.22630
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Glial-derived neurotrophic factor (Gdnf) is required for morphogenesis of the enteric nervous system (ENS) and it has been shown to regulate proliferation, differentiation, and survival of cultured enteric neural crest-derived cells (ENCCs). The goal of this study was to investigate its in vivo role in the colon, the site most commonly affected by intestinal neuropathies such as Hirschsprung's disease. Gdnf activity was modulated in ovo in the distal gut of avian embryos using targeted retrovirus-mediated gene overexpression and retroviral vector-based gene silencing. We find that Gdnf has a pleiotropic effect on colonic ENCCs, promoting proliferation, inducing neuronal differentiation, and acting as a chemoattractant. Down-regulating Gdnf similarly induces premature neuronal differentiation, but also inhibits ENCC proliferation, leading to distal colorectal aganglionosis with severe proximal hypoganglionosis. These results indicate an important role for Gdnf signaling in colonic ENS formation and emphasize the critical balance between proliferation and differentiation in the developing ENS. Developmental Dynamics 240:1402-1411, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:1402 / 1411
页数:10
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