BAPS prize-2000 - Localization and endothelin-3 dependence of stem cells of the enteric nervous system in the embryonic colon

被引:35
作者
Sidebotham, EL
Woodward, MN
Kenny, SE
Lloyd, DA
Vaillant, CR
Edgar, DH
机构
[1] Alder Hey Childrens Hosp, Dept Paediat Surg, Inst Child Hlth, Liverpool L12 2AP, Merseyside, England
[2] Univ Liverpool, Dept Human Anat, Liverpool L69 3BX, Merseyside, England
[3] Univ Liverpool, Dept Vet Preclin Sci, Liverpool L69 3BX, Merseyside, England
关键词
Hirschsprung's disease; neural crest; enteric nervous system; endothelin-3;
D O I
10.1053/jpsu.2002.30239
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background/Purpose: The aganglionosis in a variable length of the distal gut found in Hirschsprung's disease results from the abnormal prenatal development of neural crest-derived stem cells of the enteric nervous system. The cytokine endothelin-3 is necessary for successful colonization of the distal gut, but the location of this interaction with neural crest-derived stem cells remains to be established. The hypothesis tested here is that the stem cells of the enteric nervous system (ENS) in the colon are located at the leading edge of the migrating wave of neural crest-derived stem cells and that these cells require colonic endothelin-3 for complete colonization of the gut. Methods: Explants of 11.5-day-old embryonic intact mouse gut and isolated colon were cultured for 72 hours in the presence and absence of the endothelin-B receptor antagonist, BQ788. Specimens then were sectioned and stained by immunohistochemistry to assess enteric nervous system development. Results: Isolated colon contained a very low number (mean, 73 cells; range, 37 to 106; n = 8) of neural crest-derived stem cells, which had just entered its proximal end at the leading edge of neural crest cell migration. After 72 hours of culture, progeny of these few neural crest-derived stem cells had colonized the colon at an equivalent ganglionic density to those in intact gut. Furthermore, neuronal differentiation, as shown by the appearance of nitric oxide synthase positive neurons, also was equivalent to intact gut. Blockade of the endothelin-B receptor produced terminal aganglionosis in both isolated colons and intact gut. Conclusions: The very small number of cells that first enter the proximal colon at the leading edge of neural crest cell migration have the ability to colonize the entire colon normally in an ET-3-dependent manner. These cells therefore have the functional characteristics expected of the stem cells of the colonic enteric nervous system. Furthermore, the normal development of these cells is dependent on the endothelin-3 expressed by the mesenchymal cells of the colon itself. Copyright (C) 2002 by W.B. Saunders Company.
引用
收藏
页码:145 / 150
页数:6
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