Heterogeneity and Phenotypic Plasticity of Glial Cells in the Mammalian Enteric Nervous System

被引:210
作者
Boesmans, Werend [1 ]
Lasrado, Reena [2 ]
Vanden Berghe, Pieter [1 ]
Pachnis, Vassilis [2 ]
机构
[1] Univ Leuven, Lab Enter Neurosci LENS, TARGID, Dept Clin & Expt Med, B-3000 Leuven, Belgium
[2] MRC Natl Inst Med Res NIMR, Div Mol Neurobiol, London, England
基金
英国医学研究理事会;
关键词
enteric glia; enteric nervous system; neural crest; Ca2+ imaging; MOUSE MODEL; GUINEA-PIG; MYENTERIC PLEXUS; NEURON; MARKERS; COMMUNICATION; POPULATIONS; EXPRESSION; CULTURE; HEALTH;
D O I
10.1002/glia.22746
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Enteric glial cells are vital for the autonomic control of gastrointestinal homeostasis by the enteric nervous system. Several different functions have been assigned to enteric glial cells but whether these are performed by specialized subtypes with a distinctive phenotype and function remains elusive. We used Mosaic Analysis with Double Markers and inducible lineage tracing to characterize the morphology and dynamic molecular marker expression of enteric GLIA in the myenteric plexus. Functional analysis in individually identified enteric glia was performed by Ca2+ imaging. Our experiments have identified four morphologically distinct subpopulations of enteric glia in the gastrointestinal tract of adult mice. Marker expression analysis showed that the majority of glia in the myenteric plexus co-express glial fibrillary acidic protein (GFAP), S100, and Sox10. However, a considerable fraction (up to 80%) of glia outside the myenteric ganglia, did not label for these markers. Lineage tracing experiments suggest that these alternative combinations of markers reflect dynamic gene regulation rather than lineage restrictions. At the functional level, the three myenteric glia subtypes can be distinguished by their differential response to adenosine triphosphate. Together, our studies reveal extensive heterogeneity and phenotypic plasticity of enteric glial cells and set a framework for further investigations aimed at deciphering their role in digestive function and disease. GLIA 2015;63:229-241
引用
收藏
页码:229 / 241
页数:13
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