Trans-mesenteric neural crest cells are the principal source of the colonic enteric nervous system

被引:117
作者
Nishiyama, Chihiro [1 ]
Uesaka, Toshihiro [1 ]
Manabe, Takayuki [2 ]
Yonekura, Yohei [1 ]
Nagasawa, Takashi [3 ]
Newgreen, Donald F. [4 ]
Young, Heather M. [5 ]
Enomoto, Hideki [1 ]
机构
[1] RIKEN, Ctr Dev Biol, Lab Neuronal Differentiat & Regenerat, Kobe, Hyogo, Japan
[2] Fujita Hlth Univ, Inst Comprehens Med Sci, Div Gene Express Mech, Toyoake, Aichi, Japan
[3] Kyoto Univ, Inst Frontier Med Sci, Dept Immunobiol & Hematol, Kyoto, Japan
[4] Murdoch Children Res Inst, Parkville, Vic, Australia
[5] Univ Melbourne, Dept Anat & Neurosci, Melbourne, Vic, Australia
关键词
ENDOTHELIN RECEPTOR-B; HIRSCHSPRUNGS-DISEASE; GDNF FAMILY; RET; MIGRATION; NEURONS; GENE; PROLIFERATION; PATHOGENESIS; PRECURSORS;
D O I
10.1038/nn.3184
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cell migration is fundamental to organogenesis. During development, the enteric neural crest cells (ENCCs) that give rise to the enteric nervous system (ENS) migrate and colonize the entire length of the gut, which undergoes substantial growth and morphological rearrangement. How ENCCs adapt to such changes during migration, however, is not fully understood. Using time-lapse imaging analyses of mouse ENCCs, we show that a population of ENCCs crosses from the midgut to the hindgut via the mesentery during a developmental time period in which these gut regions are transiently juxtaposed, and that such 'trans-mesenteric' ENCCs constitute a large part of the hindgut ENS. This migratory process requires GDNF signaling, and evidence suggests that impaired trans-mesenteric migration of ENCCs may underlie the pathogenesis of Hirschsprung disease (intestinal aganglionosis). The discovery of this trans-mesenteric ENCC population provides a basis for improving our understanding of ENS development and pathogenesis.
引用
收藏
页码:1211 / U64
页数:9
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