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Platelet-derived chemokines promote skeletal muscle regeneration by guiding neutrophil recruitment to injured muscles

Skeletal muscle regeneration involves coordinated interactions between different cell types. Injection of platelet-rich plasma is circumstantially considered an aid to muscle repair but whether platelets promote regeneration beyond their role in hemostasis remains unexplored. Here, we find that sign...

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Autores principales: Graca, Flavia A., Stephan, Anna, Minden-Birkenmaier, Benjamin A., Shirinifard, Abbas, Wang, Yong-Dong, Demontis, Fabio, Labelle, Myriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203137/
https://www.ncbi.nlm.nih.gov/pubmed/37217480
http://dx.doi.org/10.1038/s41467-023-38624-0
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author Graca, Flavia A.
Stephan, Anna
Minden-Birkenmaier, Benjamin A.
Shirinifard, Abbas
Wang, Yong-Dong
Demontis, Fabio
Labelle, Myriam
author_facet Graca, Flavia A.
Stephan, Anna
Minden-Birkenmaier, Benjamin A.
Shirinifard, Abbas
Wang, Yong-Dong
Demontis, Fabio
Labelle, Myriam
author_sort Graca, Flavia A.
collection PubMed
description Skeletal muscle regeneration involves coordinated interactions between different cell types. Injection of platelet-rich plasma is circumstantially considered an aid to muscle repair but whether platelets promote regeneration beyond their role in hemostasis remains unexplored. Here, we find that signaling via platelet-released chemokines is an early event necessary for muscle repair in mice. Platelet depletion reduces the levels of the platelet-secreted neutrophil chemoattractants CXCL5 and CXCL7/PPBP. Consequently, early-phase neutrophil infiltration to injured muscles is impaired whereas later inflammation is exacerbated. Consistent with this model, neutrophil infiltration to injured muscles is compromised in male mice with Cxcl7-knockout platelets. Moreover, neo-angiogenesis and the re-establishment of myofiber size and muscle strength occurs optimally in control mice post-injury but not in Cxcl7ko mice and in neutrophil-depleted mice. Altogether, these findings indicate that platelet-secreted CXCL7 promotes regeneration by recruiting neutrophils to injured muscles, and that this signaling axis could be utilized therapeutically to boost muscle regeneration.
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spelling pubmed-102031372023-05-24 Platelet-derived chemokines promote skeletal muscle regeneration by guiding neutrophil recruitment to injured muscles Graca, Flavia A. Stephan, Anna Minden-Birkenmaier, Benjamin A. Shirinifard, Abbas Wang, Yong-Dong Demontis, Fabio Labelle, Myriam Nat Commun Article Skeletal muscle regeneration involves coordinated interactions between different cell types. Injection of platelet-rich plasma is circumstantially considered an aid to muscle repair but whether platelets promote regeneration beyond their role in hemostasis remains unexplored. Here, we find that signaling via platelet-released chemokines is an early event necessary for muscle repair in mice. Platelet depletion reduces the levels of the platelet-secreted neutrophil chemoattractants CXCL5 and CXCL7/PPBP. Consequently, early-phase neutrophil infiltration to injured muscles is impaired whereas later inflammation is exacerbated. Consistent with this model, neutrophil infiltration to injured muscles is compromised in male mice with Cxcl7-knockout platelets. Moreover, neo-angiogenesis and the re-establishment of myofiber size and muscle strength occurs optimally in control mice post-injury but not in Cxcl7ko mice and in neutrophil-depleted mice. Altogether, these findings indicate that platelet-secreted CXCL7 promotes regeneration by recruiting neutrophils to injured muscles, and that this signaling axis could be utilized therapeutically to boost muscle regeneration. Nature Publishing Group UK 2023-05-22 /pmc/articles/PMC10203137/ /pubmed/37217480 http://dx.doi.org/10.1038/s41467-023-38624-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Graca, Flavia A.
Stephan, Anna
Minden-Birkenmaier, Benjamin A.
Shirinifard, Abbas
Wang, Yong-Dong
Demontis, Fabio
Labelle, Myriam
Platelet-derived chemokines promote skeletal muscle regeneration by guiding neutrophil recruitment to injured muscles
title Platelet-derived chemokines promote skeletal muscle regeneration by guiding neutrophil recruitment to injured muscles
title_full Platelet-derived chemokines promote skeletal muscle regeneration by guiding neutrophil recruitment to injured muscles
title_fullStr Platelet-derived chemokines promote skeletal muscle regeneration by guiding neutrophil recruitment to injured muscles
title_full_unstemmed Platelet-derived chemokines promote skeletal muscle regeneration by guiding neutrophil recruitment to injured muscles
title_short Platelet-derived chemokines promote skeletal muscle regeneration by guiding neutrophil recruitment to injured muscles
title_sort platelet-derived chemokines promote skeletal muscle regeneration by guiding neutrophil recruitment to injured muscles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203137/
https://www.ncbi.nlm.nih.gov/pubmed/37217480
http://dx.doi.org/10.1038/s41467-023-38624-0
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