Department of Pediatric Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Clin Genet. 2013 Apr;83(4):307-16. doi: 10.1111/cge.12054. Epub 2012 Nov 27.
The enteric nervous system (ENS), the intrinsic innervation of the gastrointestinal tract, is an essential component of the gut neuromusculature and controls many aspects of gut function, including coordinated muscular peristalsis. The ENS is entirely derived from neural crest cells (NCC) which undergo a number of key processes, including extensive migration into and along the gut, proliferation, and differentiation into enteric neurons and glia, during embryogenesis and fetal life. These mechanisms are under the molecular control of numerous signaling pathways, transcription factors, neurotrophic factors and extracellular matrix components. Failure in these processes and consequent abnormal ENS development can result in so-called enteric neuropathies, arguably the best characterized of which is the congenital disorder Hirschsprung disease (HSCR), or aganglionic megacolon. This review focuses on the molecular and genetic factors regulating ENS development from NCC, the clinical genetics of HSCR and its associated syndromes, and recent advances aimed at improving our understanding and treatment of enteric neuropathies.
肠神经系统(ENS)是胃肠道的固有神经支配,是肠道神经肌肉的重要组成部分,控制着肠道功能的许多方面,包括协调的肌肉蠕动。ENS 完全来源于神经嵴细胞(NCC),它们在胚胎发生和胎儿期经历了许多关键过程,包括广泛的迁移到肠道内和沿着肠道迁移、增殖,并分化为肠神经元和神经胶质细胞。这些机制受到许多信号通路、转录因子、神经营养因子和细胞外基质成分的分子控制。这些过程的失败以及随之而来的 ENS 发育异常可导致所谓的肠神经病变,其中最具特征性的是先天性巨结肠症(HSCR)或无神经节细胞性巨结肠。这篇综述重点介绍了从 NCC 调节 ENS 发育的分子和遗传因素、HSCR 的临床遗传学及其相关综合征,以及旨在提高我们对肠神经病变的理解和治疗的最新进展。