Neuron–Glia Interaction in the Developing and Adult Enteric Nervous System

The enteric nervous system (ENS) constitutes the largest part of the peripheral nervous system. In recent years, ENS development and its neurogenetic capacity in homeostasis and allostasishave gained increasing attention. Developmentally, the neural precursors of the ENS are mainly derived from vaga...

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Main Authors: Verena Pawolski, Mirko H. H. Schmidt
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:Cells
Subjects:
gut
Online Access:https://www.mdpi.com/2073-4409/10/1/47
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spelling doaj-1cbcdc52af4f4d418a4220b339c6dc242021-01-01T00:00:57ZengMDPI AGCells2073-44092021-12-0110474710.3390/cells10010047Neuron–Glia Interaction in the Developing and Adult Enteric Nervous SystemVerena Pawolski0Mirko H. H. Schmidt1Institute of Anatomy, Medical Faculty Carl Gustav Carus, TechnischeUniversität Dresden School of Medicine, 01307 Dresden, GermanyInstitute of Anatomy, Medical Faculty Carl Gustav Carus, TechnischeUniversität Dresden School of Medicine, 01307 Dresden, GermanyThe enteric nervous system (ENS) constitutes the largest part of the peripheral nervous system. In recent years, ENS development and its neurogenetic capacity in homeostasis and allostasishave gained increasing attention. Developmentally, the neural precursors of the ENS are mainly derived from vagal and sacral neural crest cell portions. Furthermore, Schwann cell precursors, as well as endodermal pancreatic progenitors, participate in ENS formation. Neural precursorsenherite three subpopulations: a bipotent neuron-glia, a neuronal-fated and a glial-fated subpopulation. Typically, enteric neural precursors migrate along the entire bowel to the anal end, chemoattracted by glial cell-derived neurotrophic factor (GDNF) and endothelin 3 (EDN3) molecules. During migration, a fraction undergoes differentiation into neurons and glial cells. Differentiation is regulated by bone morphogenetic proteins (BMP), Hedgehog and Notch signalling. The fully formed adult ENS may react to injury and damage with neurogenesis and gliogenesis. Nevertheless, the origin of differentiating cells is currently under debate. Putative candidates are an embryonic-like enteric neural progenitor population, Schwann cell precursors and transdifferentiating glial cells. These cells can be isolated and propagated in culture as adult ENS progenitors and may be used for cell transplantation therapies for treating enteric aganglionosis in Chagas and Hirschsprung’s diseases.https://www.mdpi.com/2073-4409/10/1/47neuron-glia interactionneural crest cellsenteric nervous systemgastrointestinal systemgutGDNF
collection DOAJ
language English
format Article
sources DOAJ
author Verena Pawolski
Mirko H. H. Schmidt
spellingShingle Verena Pawolski
Mirko H. H. Schmidt
Neuron–Glia Interaction in the Developing and Adult Enteric Nervous System
Cells
neuron-glia interaction
neural crest cells
enteric nervous system
gastrointestinal system
gut
GDNF
author_facet Verena Pawolski
Mirko H. H. Schmidt
author_sort Verena Pawolski
title Neuron–Glia Interaction in the Developing and Adult Enteric Nervous System
title_short Neuron–Glia Interaction in the Developing and Adult Enteric Nervous System
title_full Neuron–Glia Interaction in the Developing and Adult Enteric Nervous System
title_fullStr Neuron–Glia Interaction in the Developing and Adult Enteric Nervous System
title_full_unstemmed Neuron–Glia Interaction in the Developing and Adult Enteric Nervous System
title_sort neuron–glia interaction in the developing and adult enteric nervous system
publisher MDPI AG
series Cells
issn 2073-4409
publishDate 2021-12-01
description The enteric nervous system (ENS) constitutes the largest part of the peripheral nervous system. In recent years, ENS development and its neurogenetic capacity in homeostasis and allostasishave gained increasing attention. Developmentally, the neural precursors of the ENS are mainly derived from vagal and sacral neural crest cell portions. Furthermore, Schwann cell precursors, as well as endodermal pancreatic progenitors, participate in ENS formation. Neural precursorsenherite three subpopulations: a bipotent neuron-glia, a neuronal-fated and a glial-fated subpopulation. Typically, enteric neural precursors migrate along the entire bowel to the anal end, chemoattracted by glial cell-derived neurotrophic factor (GDNF) and endothelin 3 (EDN3) molecules. During migration, a fraction undergoes differentiation into neurons and glial cells. Differentiation is regulated by bone morphogenetic proteins (BMP), Hedgehog and Notch signalling. The fully formed adult ENS may react to injury and damage with neurogenesis and gliogenesis. Nevertheless, the origin of differentiating cells is currently under debate. Putative candidates are an embryonic-like enteric neural progenitor population, Schwann cell precursors and transdifferentiating glial cells. These cells can be isolated and propagated in culture as adult ENS progenitors and may be used for cell transplantation therapies for treating enteric aganglionosis in Chagas and Hirschsprung’s diseases.
topic neuron-glia interaction
neural crest cells
enteric nervous system
gastrointestinal system
gut
GDNF
url https://www.mdpi.com/2073-4409/10/1/47
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