Druckenbrod Noah R, Powers Patricia A, Bartley Christopher R, Walker Jeffery W, Epstein Miles L
Department of Anatomy, School of Medicine and Public Health, University of Wisconsin, Madison, Wisconsin 53706, USA.
Genesis. 2008 Aug;46(8):396-400. doi: 10.1002/dvg.20415.
Endothelin receptor B (Ednrb) plays a critical role in the development of melanocytes and neurons and glia of the enteric nervous system. These distinct neural crest-derived cell types express Ednrb and share the property of intercalating into tissues, such as the intestine whose muscle precursor cells also express Ednrb. Such widespread Ednrb expression has been a significant obstacle in establishing precise roles for Ednrb in development. We describe here the production of an Ednrb allele floxed at exon 3 and its use in excising the receptor from mouse neural crest cells by use of Cre-recombinase driven by the Wnt1 promoter. Mice born with neural crest-specific excision of Ednrb possess aganglionic colon, lack trunk pigmentation, and die within 5 weeks due to megacolon. Ednrb receptor expression in these animals is absent only in the neural crest but present in surrounding smooth muscle cells. The absence of Ednrb from crest cells also results in a compensatory upregulation of Ednrb expression in other cells within the gut. We conclude that Ednrb loss only in neural crest cells is sufficient to produce the Hirschsprungs disease phenotype observed with genomic Ednrb mutations.
内皮素受体B(Ednrb)在黑素细胞以及肠神经系统的神经元和神经胶质细胞的发育中起关键作用。这些源自神经嵴的不同细胞类型表达Ednrb,并具有插入组织的特性,例如其肌肉前体细胞也表达Ednrb的肠道。这种广泛的Ednrb表达一直是确定Ednrb在发育中的确切作用的重大障碍。我们在此描述了一个在第3外显子处被floxed的Ednrb等位基因的产生,以及通过使用由Wnt1启动子驱动的Cre重组酶从小鼠神经嵴细胞中切除该受体的用途。出生时神经嵴特异性切除Ednrb的小鼠患有无神经节结肠,缺乏躯干色素沉着,并因巨结肠在5周内死亡。这些动物中Ednrb受体的表达仅在神经嵴中缺失,但在周围的平滑肌细胞中存在。神经嵴细胞中Ednrb的缺失也导致肠道内其他细胞中Ednrb表达的代偿性上调。我们得出结论,仅神经嵴细胞中Ednrb的缺失就足以产生与基因组Ednrb突变相关的先天性巨结肠病表型。