Enteric nervous system development: A crest cell's journey from neural tube to colon

被引:137
|
作者
Nagy, Nandor [1 ,2 ,3 ]
Goldstein, Allan M. [1 ,2 ]
机构
[1] Harvard Med Sch, Massachusetts Gen Hosp, Dept Pediat Surg, Boston, MA USA
[2] Massachusetts Gen Hosp, Ctr Neurointestinal Hlth, Boston, MA 02114 USA
[3] Semmelweis Univ, Fac Med, Dept Anat Histol & Embryol, Budapest, Hungary
基金
美国国家卫生研究院;
关键词
Enteric nervous system; Gut development; Neural crest; Hirschsprung disease; RECEPTOR TYROSINE KINASE; ENDOTHELIN-B RECEPTOR; SONIC-HEDGEHOG; HIRSCHSPRUNG-DISEASE; C-RET; EXTRACELLULAR-MATRIX; PRECURSOR MIGRATION; PROGENITOR CELLS; MICE LACKING; INTESTINAL AGANGLIONOSIS;
D O I
10.1016/j.semcdb.2017.01.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:94 / 106
页数:13
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