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先天性巨结肠症及其变异型的发病机制:最新进展

Pathogenesis of Hirschsprung's disease and its variants: recent progress.

作者信息

Puri Prem, Shinkai Toko

机构信息

Children's Research Centre, Our Lady's Hospital for Sick Children, University College Dublin, Ireland.

出版信息

Semin Pediatr Surg. 2004 Feb;13(1):18-24. doi: 10.1053/j.sempedsurg.2003.09.004.

Abstract

The enteric nervous system (ENS) is a complex network of interconnected neurons within the wall of the intestine that controls intestinal motility, regulates mucosal secretion and blood flow, and also modulates sensation from the gut. The cells that form the ENS in mammals are derived primarily from vagal neural crest cells. During the past decade there has been an explosion of information about genes that control the development of neural crest. Molecular-genetic analysis has identified several genes that have a role in the development of Hirschsprung's disease. The major susceptibility gene is RET, which is also involved in multiple endocrine neoplasia type 2. Recently, genetic studies have provided strong evidence in animal models that intestinal neuronal dysplasia (IND) is a real entity. HOX11L1 knockout mice and endothelin B receptor-deficient rats demonstrated abnormalities of the ENS resembling IND type B in humans. These findings support the concept that IND may be linked to a genetic defect.

摘要

肠神经系统(ENS)是肠道壁内相互连接的神经元组成的复杂网络,它控制肠道蠕动,调节黏膜分泌和血流,还能调节来自肠道的感觉。哺乳动物中形成ENS的细胞主要来源于迷走神经嵴细胞。在过去十年里,关于控制神经嵴发育的基因的信息大量涌现。分子遗传学分析已经鉴定出几个在先天性巨结肠症发育中起作用的基因。主要的易感基因是RET,它也与2型多发性内分泌肿瘤有关。最近,遗传学研究在动物模型中提供了有力证据,证明肠道神经元发育异常(IND)是一种真实的病症。HOX11L1基因敲除小鼠和内皮素B受体缺陷大鼠表现出与人类IND B型相似的ENS异常。这些发现支持了IND可能与遗传缺陷有关的观点。

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