Nagy Nandor, Goldstein Allan M
Department of Pediatric Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States; Center for Neurointestinal Health, Massachusetts General Hospital, Boston, MA, United States; Department of Anatomy, Histology and Embryology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Department of Pediatric Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States; Center for Neurointestinal Health, Massachusetts General Hospital, Boston, MA, United States.
Semin Cell Dev Biol. 2017 Jun;66:94-106. doi: 10.1016/j.semcdb.2017.01.006. Epub 2017 Jan 10.
The enteric nervous system (ENS) is comprised of a network of neurons and glial cells that are responsible for coordinating many aspects of gastrointestinal (GI) function. These cells arise from the neural crest, migrate to the gut, and then continue their journey to colonize the entire length of the GI tract. Our understanding of the molecular and cellular events that regulate these processes has advanced significantly over the past several decades, in large part facilitated by the use of rodents, avians, and zebrafish as model systems to dissect the signals and pathways involved. These studies have highlighted the highly dynamic nature of ENS development and the importance of carefully balancing migration, proliferation, and differentiation of enteric neural crest-derived cells (ENCCs). Proliferation, in particular, is critically important as it drives cell density and speed of migration, both of which are important for ensuring complete colonization of the gut. However, proliferation must be tempered by differentiation among cells that have reached their final destination and are ready to send axonal extensions, connect to effector cells, and begin to produce neurotransmitters or other signals. Abnormalities in the normal processes guiding ENCC development can lead to failure of ENS formation, as occurs in Hirschsprung disease, in which the distal intestine remains aganglionic. This review summarizes our current understanding of the factors involved in early development of the ENS and discusses areas in need of further investigation.
肠神经系统(ENS)由神经元和神经胶质细胞网络组成,负责协调胃肠道(GI)功能的许多方面。这些细胞起源于神经嵴,迁移至肠道,然后继续其行程以定植于胃肠道的全长。在过去几十年中,我们对调节这些过程的分子和细胞事件的理解有了显著进展,这在很大程度上得益于使用啮齿动物、鸟类和斑马鱼作为模型系统来剖析所涉及的信号和途径。这些研究突出了ENS发育的高度动态性质以及仔细平衡肠神经嵴衍生细胞(ENCCs)的迁移、增殖和分化的重要性。特别是增殖至关重要,因为它驱动细胞密度和迁移速度,这两者对于确保肠道完全定植都很重要。然而,对于已到达最终目的地并准备好发出轴突延伸、连接到效应细胞并开始产生神经递质或其他信号的细胞,增殖必须受到分化的调节。指导ENCC发育的正常过程中的异常可导致ENS形成失败,如先天性巨结肠病中发生的那样,其中远端肠道仍然无神经节。本综述总结了我们目前对ENS早期发育所涉及因素的理解,并讨论了需要进一步研究的领域。