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

• Published in: Journal of pediatric surgery 2002-02, Vol.37 (2), p.145-150
• Main Authors: Sidebotham, Emma L., Woodward, Mark N., Kenny, Simon E., Lloyd, David A., Vaillant, Camille R., Edgar, David H.
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Cell Movement - drug effects; Cells, Cultured; Colon - cytology; Colon - embryology; Colon - innervation; Disease Models, Animal; endothelin-3; Endothelin-3 - analysis; Endothelin-3 - physiology; enteric nervous system; Enteric Nervous System - cytology; Enteric Nervous System - embryology; Enteric Nervous System - physiology; Gastroenterology. Liver. Pancreas. Abdomen; Hirschsprung Disease - embryology; Hirschsprung Disease - physiopathology; Hirschsprung's disease; Malformations; Medical sciences; Mice; neural crest; Neural Crest - cytology; Neural Crest - embryology; Oligopeptides - pharmacology; Piperidines - pharmacology; Stem Cells - chemistry; Stem Cells - cytology; Stem Cells - drug effects; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
• ISSN: 0022-3468; 1531-5037
• DOI: 10.1053/jpsu.2002.30239

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. J Pediatr Surg 37:145-150. Copyright © 2002 by W.B. Saunders Company.