Genetic model system studies of the development of the enteric nervous system, gut motility and Hirschsprung's disease

被引:58
作者
Burzynski, G. [1 ]
Shepherd, I. T. [1 ]
Enomoto, H. [2 ]
机构
[1] Emory Univ, Dept Biol, Atlanta, GA 30322 USA
[2] RIKEN Ctr Dev Biol, Lab Neural Differentiat & Regenerat, Kobe, Hyogo, Japan
关键词
enteric neurons; mouse; neural crest; screens; transgenics; zebrafish; NEURAL CREST CELLS; RECEPTOR TYROSINE KINASE; ENDOTHELIN-B RECEPTOR; DANIO-RERIO EMBRYOS; MICE LACKING; INTERSTITIAL-CELLS; NEUROTROPHIC FACTOR; SONIC HEDGEHOG; MOUSE MODEL; RET GENE;
D O I
10.1111/j.1365-2982.2008.01256.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The enteric nervous system (ENS) is the largest and most complicated subdivision of the peripheral nervous system. Its action is necessary to regulate many of the functions of the gastrointestinal tract including its motility. Whilst the ENS has been studied extensively by developmental biologists, neuroscientists and physiologists for several decades it has only been since the early 1990s that the molecular and genetic basis of ENS development has begun to emerge. Central to this understanding has been the use of genetic model organisms. In this article, we will discuss recent advances that have been achieved using both mouse and zebrafish model genetic systems that have led to new insights into ENS development and the genetic basis of Hirschsprung's disease.
引用
收藏
页码:113 / 127
页数:15
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