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肠神经系统。

The enteric nervous system.

机构信息

Division of Molecular Neurobiology, MRC National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, UK.

出版信息

Dev Biol. 2012 Jun 1;366(1):64-73. doi: 10.1016/j.ydbio.2012.01.012. Epub 2012 Jan 24.

Abstract

The enteric nervous system (ENS), the intrinsic innervation of the gastrointestinal tract, consists of numerous types of neurons, and glial cells, that are distributed in two intramuscular plexuses that extend along the entire length of the gut and control co-ordinated smooth muscle contractile activity and other gut functions. All enteric neurons and glia are derived from neural crest cells (NCC). Vagal (hindbrain) level NCC provide the majority of enteric precursors along the entire length of the gut, while a lesser contribution, that is restricted to the hindgut, arises from the sacral region of the neuraxis. After leaving the dorsal neural tube NCC undergo extensive migration, proliferation, survival and differentiation in order to form a functional ENS. This article reviews the molecular mechanisms underlying these key developmental processes and highlights the major groups of molecules that affect enteric NCC proliferation and survival (Ret/Gdnf and EdnrB/Et-3 pathways, Sox10 and Phox2b transcription factors), cell migration (Ret and EdnrB signalling, semaphorin 3A, cell adhesion molecules, Rho GTPases), and the development of enteric neuronal subtypes and morphologies (Mash1, Gdnf/neurturin, BMPs, Hand2, retinoic acid). Finally, looking to the future, we discuss the need to translate the wealth of data gleaned from animal studies to the clinical area and thus better understand, and develop treatments for, congenital human diseases affecting the ENS.

摘要

肠神经系统(ENS)是胃肠道的固有神经支配,由分布在两个沿肠道全长延伸的肌间神经丛中的众多神经元和神经胶质细胞组成,控制协调的平滑肌收缩活动和其他肠道功能。所有肠神经元和神经胶质细胞都来源于神经嵴细胞(NCC)。迷走神经(后脑)水平的 NCC 提供了肠道全长的大部分肠前体细胞,而较少的一部分(仅限于后肠)则来自轴突的骶区。离开背侧神经管后,NCC 经历广泛的迁移、增殖、存活和分化,以形成功能齐全的 ENS。本文综述了这些关键发育过程背后的分子机制,并强调了影响肠 NCC 增殖和存活的主要分子群(Ret/Gdnf 和 EdnrB/Et-3 途径、Sox10 和 Phox2b 转录因子)、细胞迁移(Ret 和 EdnrB 信号、Semaphorin 3A、细胞黏附分子、Rho GTPases)以及肠神经元亚型和形态发生(Mash1、Gdnf/neurturin、BMPs、Hand2、视黄酸)。最后,展望未来,我们讨论了将从动物研究中获得的大量数据转化为临床领域的必要性,从而更好地理解和开发治疗先天性人类 ENS 疾病的方法。

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