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The chemokines CXCL12 and CXCL14 differentially regulate connective tissue markers during limb development
Connective tissues (CT) support and connect organs together. Understanding the formation of CT is important, as CT deregulation leads to fibrosis. The identification of CT specific markers has contributed to a better understanding of CT function during development. In developing limbs, Osr1 transcri...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722906/ https://www.ncbi.nlm.nih.gov/pubmed/29222527 http://dx.doi.org/10.1038/s41598-017-17490-z |
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author | Nassari, Sonya Blavet, Cédrine Bonnin, Marie-Ange Stricker, Sigmar Duprez, Delphine Fournier-Thibault, Claire |
author_facet | Nassari, Sonya Blavet, Cédrine Bonnin, Marie-Ange Stricker, Sigmar Duprez, Delphine Fournier-Thibault, Claire |
author_sort | Nassari, Sonya |
collection | PubMed |
description | Connective tissues (CT) support and connect organs together. Understanding the formation of CT is important, as CT deregulation leads to fibrosis. The identification of CT specific markers has contributed to a better understanding of CT function during development. In developing limbs, Osr1 transcription factor is involved in the differentiation of irregular CT while the transcription factor Scx labels tendon. In this study, we show that the CXCL12 and CXCL14 chemokines display distinct expression pattern in limb CT during chick development. CXCL12 positively regulates the expression of OSR1 and COL3A1, a collagen subtype of irregular CT, while CXCL14 activates the expression of the tendon marker SCX. We provide evidence that the CXCL12 effect on irregular CT involves CXCR4 receptor and vessels. In addition, the expression of CXCL12, CXCL14 and OSR genes is suppressed by the anti-fibrotic BMP signal. Finally, mechanical forces, known to be involved in adult fibrosis, control the expression of chemokines, CT-associated transcription factors and collagens during limb development. Such unexpected roles of CXCL12 and CXCL14 chemokines during CT differentiation can contribute to a better understanding of the fibrosis mechanisms in adult pathological conditions. |
format | Online Article Text |
id | pubmed-5722906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57229062017-12-12 The chemokines CXCL12 and CXCL14 differentially regulate connective tissue markers during limb development Nassari, Sonya Blavet, Cédrine Bonnin, Marie-Ange Stricker, Sigmar Duprez, Delphine Fournier-Thibault, Claire Sci Rep Article Connective tissues (CT) support and connect organs together. Understanding the formation of CT is important, as CT deregulation leads to fibrosis. The identification of CT specific markers has contributed to a better understanding of CT function during development. In developing limbs, Osr1 transcription factor is involved in the differentiation of irregular CT while the transcription factor Scx labels tendon. In this study, we show that the CXCL12 and CXCL14 chemokines display distinct expression pattern in limb CT during chick development. CXCL12 positively regulates the expression of OSR1 and COL3A1, a collagen subtype of irregular CT, while CXCL14 activates the expression of the tendon marker SCX. We provide evidence that the CXCL12 effect on irregular CT involves CXCR4 receptor and vessels. In addition, the expression of CXCL12, CXCL14 and OSR genes is suppressed by the anti-fibrotic BMP signal. Finally, mechanical forces, known to be involved in adult fibrosis, control the expression of chemokines, CT-associated transcription factors and collagens during limb development. Such unexpected roles of CXCL12 and CXCL14 chemokines during CT differentiation can contribute to a better understanding of the fibrosis mechanisms in adult pathological conditions. Nature Publishing Group UK 2017-12-08 /pmc/articles/PMC5722906/ /pubmed/29222527 http://dx.doi.org/10.1038/s41598-017-17490-z Text en © The Author(s) 2017 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 Nassari, Sonya Blavet, Cédrine Bonnin, Marie-Ange Stricker, Sigmar Duprez, Delphine Fournier-Thibault, Claire The chemokines CXCL12 and CXCL14 differentially regulate connective tissue markers during limb development |
title | The chemokines CXCL12 and CXCL14 differentially regulate connective tissue markers during limb development |
title_full | The chemokines CXCL12 and CXCL14 differentially regulate connective tissue markers during limb development |
title_fullStr | The chemokines CXCL12 and CXCL14 differentially regulate connective tissue markers during limb development |
title_full_unstemmed | The chemokines CXCL12 and CXCL14 differentially regulate connective tissue markers during limb development |
title_short | The chemokines CXCL12 and CXCL14 differentially regulate connective tissue markers during limb development |
title_sort | chemokines cxcl12 and cxcl14 differentially regulate connective tissue markers during limb development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722906/ https://www.ncbi.nlm.nih.gov/pubmed/29222527 http://dx.doi.org/10.1038/s41598-017-17490-z |
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