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Cxcr4 and Sdf-1 are critically involved in the formation of facial and non-somitic neck muscles
The present study shows that the CXCR4/SDF-1 axis regulates the migration of second branchial arch-derived muscles as well as non-somitic neck muscles. Cxcr4 is expressed by skeletal muscle progenitor cells in the second branchial arch (BA2). Muscles derived from the second branchial arch, but not f...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081242/ https://www.ncbi.nlm.nih.gov/pubmed/32193486 http://dx.doi.org/10.1038/s41598-020-61960-w |
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author | Yahya, Imadeldin Böing, Marion Pu, Qin Puchert, Malte Oedemis, Veysel Engele, Jürgen Brand-Saberi, Beate Morosan-Puopolo, Gabriela |
author_facet | Yahya, Imadeldin Böing, Marion Pu, Qin Puchert, Malte Oedemis, Veysel Engele, Jürgen Brand-Saberi, Beate Morosan-Puopolo, Gabriela |
author_sort | Yahya, Imadeldin |
collection | PubMed |
description | The present study shows that the CXCR4/SDF-1 axis regulates the migration of second branchial arch-derived muscles as well as non-somitic neck muscles. Cxcr4 is expressed by skeletal muscle progenitor cells in the second branchial arch (BA2). Muscles derived from the second branchial arch, but not from the first, fail to form in Cxcr4 mutants at embryonic days E13.5 and E14.5. Cxcr4 is also required for the development of non-somitic neck muscles. In Cxcr4 mutants, non-somitic neck muscle development is severely perturbed. In vivo experiments in chicken by means of loss-of-function approach based on the application of beads loaded with the CXCR4 inhibitor AMD3100 into the cranial paraxial mesoderm resulted in decreased expression of Tbx1 in the BA2. Furthermore, disrupting this chemokine signal at a later stage by implanting these beads into the BA2 caused a reduction in MyoR, Myf5 and MyoD expression. In contrast, gain-of-function experiments based on the implantation of SDF-1 beads into BA2 resulted in an attraction of myogenic progenitor cells, which was reflected in an expansion of the expression domain of these myogenic markers towards the SDF-1 source. Thus, Cxcr4 is required for the formation of the BA2 derived muscles and non-somitic neck muscles. |
format | Online Article Text |
id | pubmed-7081242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70812422020-03-23 Cxcr4 and Sdf-1 are critically involved in the formation of facial and non-somitic neck muscles Yahya, Imadeldin Böing, Marion Pu, Qin Puchert, Malte Oedemis, Veysel Engele, Jürgen Brand-Saberi, Beate Morosan-Puopolo, Gabriela Sci Rep Article The present study shows that the CXCR4/SDF-1 axis regulates the migration of second branchial arch-derived muscles as well as non-somitic neck muscles. Cxcr4 is expressed by skeletal muscle progenitor cells in the second branchial arch (BA2). Muscles derived from the second branchial arch, but not from the first, fail to form in Cxcr4 mutants at embryonic days E13.5 and E14.5. Cxcr4 is also required for the development of non-somitic neck muscles. In Cxcr4 mutants, non-somitic neck muscle development is severely perturbed. In vivo experiments in chicken by means of loss-of-function approach based on the application of beads loaded with the CXCR4 inhibitor AMD3100 into the cranial paraxial mesoderm resulted in decreased expression of Tbx1 in the BA2. Furthermore, disrupting this chemokine signal at a later stage by implanting these beads into the BA2 caused a reduction in MyoR, Myf5 and MyoD expression. In contrast, gain-of-function experiments based on the implantation of SDF-1 beads into BA2 resulted in an attraction of myogenic progenitor cells, which was reflected in an expansion of the expression domain of these myogenic markers towards the SDF-1 source. Thus, Cxcr4 is required for the formation of the BA2 derived muscles and non-somitic neck muscles. Nature Publishing Group UK 2020-03-19 /pmc/articles/PMC7081242/ /pubmed/32193486 http://dx.doi.org/10.1038/s41598-020-61960-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yahya, Imadeldin Böing, Marion Pu, Qin Puchert, Malte Oedemis, Veysel Engele, Jürgen Brand-Saberi, Beate Morosan-Puopolo, Gabriela Cxcr4 and Sdf-1 are critically involved in the formation of facial and non-somitic neck muscles |
title | Cxcr4 and Sdf-1 are critically involved in the formation of facial and non-somitic neck muscles |
title_full | Cxcr4 and Sdf-1 are critically involved in the formation of facial and non-somitic neck muscles |
title_fullStr | Cxcr4 and Sdf-1 are critically involved in the formation of facial and non-somitic neck muscles |
title_full_unstemmed | Cxcr4 and Sdf-1 are critically involved in the formation of facial and non-somitic neck muscles |
title_short | Cxcr4 and Sdf-1 are critically involved in the formation of facial and non-somitic neck muscles |
title_sort | cxcr4 and sdf-1 are critically involved in the formation of facial and non-somitic neck muscles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081242/ https://www.ncbi.nlm.nih.gov/pubmed/32193486 http://dx.doi.org/10.1038/s41598-020-61960-w |
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