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CXCR4/SDF1 signalling promotes sensory neuron clustering in vitro

During the development of the peripheral nervous system, a subgroup of neural crest cells migrate away from the neural tube and coalesce into clusters of sensory neurons (ganglia). Mechanisms involved in the formation of the dorsal root ganglia (DRG) from neural crest cells are currently unclear. Mi...

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Autores principales: Terheyden-Keighley, Daniel, Zhang, Xiaoqing, Brand-Saberi, Beate, Theiss, Carsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176946/
https://www.ncbi.nlm.nih.gov/pubmed/30135081
http://dx.doi.org/10.1242/bio.035568
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author Terheyden-Keighley, Daniel
Zhang, Xiaoqing
Brand-Saberi, Beate
Theiss, Carsten
author_facet Terheyden-Keighley, Daniel
Zhang, Xiaoqing
Brand-Saberi, Beate
Theiss, Carsten
author_sort Terheyden-Keighley, Daniel
collection PubMed
description During the development of the peripheral nervous system, a subgroup of neural crest cells migrate away from the neural tube and coalesce into clusters of sensory neurons (ganglia). Mechanisms involved in the formation of the dorsal root ganglia (DRG) from neural crest cells are currently unclear. Mice carrying mutations in Cxcr4, which is known to control neural crest migration, exhibit malformed DRG. In order to investigate this phenomenon, we modelled sensory neuron differentiation in vitro by directing the differentiation of human induced pluripotent stem cells into sensory neurons under SDF1 (agonist), AMD3100 (antagonist) or control conditions. There we could show a marked effect on the clustering activity of the neurons in vitro, suggesting that CXCR4 signalling is involved in facilitating DRG condensation.
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spelling pubmed-61769462018-10-11 CXCR4/SDF1 signalling promotes sensory neuron clustering in vitro Terheyden-Keighley, Daniel Zhang, Xiaoqing Brand-Saberi, Beate Theiss, Carsten Biol Open Research Article During the development of the peripheral nervous system, a subgroup of neural crest cells migrate away from the neural tube and coalesce into clusters of sensory neurons (ganglia). Mechanisms involved in the formation of the dorsal root ganglia (DRG) from neural crest cells are currently unclear. Mice carrying mutations in Cxcr4, which is known to control neural crest migration, exhibit malformed DRG. In order to investigate this phenomenon, we modelled sensory neuron differentiation in vitro by directing the differentiation of human induced pluripotent stem cells into sensory neurons under SDF1 (agonist), AMD3100 (antagonist) or control conditions. There we could show a marked effect on the clustering activity of the neurons in vitro, suggesting that CXCR4 signalling is involved in facilitating DRG condensation. The Company of Biologists Ltd 2018-08-22 /pmc/articles/PMC6176946/ /pubmed/30135081 http://dx.doi.org/10.1242/bio.035568 Text en © 2018. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Terheyden-Keighley, Daniel
Zhang, Xiaoqing
Brand-Saberi, Beate
Theiss, Carsten
CXCR4/SDF1 signalling promotes sensory neuron clustering in vitro
title CXCR4/SDF1 signalling promotes sensory neuron clustering in vitro
title_full CXCR4/SDF1 signalling promotes sensory neuron clustering in vitro
title_fullStr CXCR4/SDF1 signalling promotes sensory neuron clustering in vitro
title_full_unstemmed CXCR4/SDF1 signalling promotes sensory neuron clustering in vitro
title_short CXCR4/SDF1 signalling promotes sensory neuron clustering in vitro
title_sort cxcr4/sdf1 signalling promotes sensory neuron clustering in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176946/
https://www.ncbi.nlm.nih.gov/pubmed/30135081
http://dx.doi.org/10.1242/bio.035568
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