Direct contribution of skeletal muscle mesenchymal progenitors to bone repair.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
17 05 2021
Historique:
received: 04 02 2020
accepted: 29 03 2021
entrez: 18 5 2021
pubmed: 19 5 2021
medline: 8 6 2021
Statut: epublish

Résumé

Bone regenerates by activation of tissue resident stem/progenitor cells, formation of a fibrous callus followed by deposition of cartilage and bone matrices. Here, we show that mesenchymal progenitors residing in skeletal muscle adjacent to bone mediate the initial fibrotic response to bone injury and also participate in cartilage and bone formation. Combined lineage and single-cell RNA sequencing analyses reveal that skeletal muscle mesenchymal progenitors adopt a fibrogenic fate before they engage in chondrogenesis after fracture. In polytrauma, where bone and skeletal muscle are injured, skeletal muscle mesenchymal progenitors exhibit altered fibrogenesis and chondrogenesis. This leads to impaired bone healing, which is due to accumulation of fibrotic tissue originating from skeletal muscle and can be corrected by the anti-fibrotic agent Imatinib. These results elucidate the central role of skeletal muscle in bone regeneration and provide evidence that skeletal muscle can be targeted to prevent persistent callus fibrosis and improve bone healing after musculoskeletal trauma.

Identifiants

pubmed: 34001878
doi: 10.1038/s41467-021-22842-5
pii: 10.1038/s41467-021-22842-5
pmc: PMC8128920
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2860

Subventions

Organisme : NIAMS NIH HHS
ID : R01 AR057344
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR072707
Pays : United States

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Auteurs

Anais Julien (A)

Univ Paris Est Creteil, INSERM, IMRB, Creteil, France.

Anuya Kanagalingam (A)

Univ Paris Est Creteil, INSERM, IMRB, Creteil, France.

Ester Martínez-Sarrà (E)

Univ Paris Est Creteil, INSERM, IMRB, Creteil, France.

Jérome Megret (J)

Cytometry core facility, Structure Fédérative de Recherche Necker, INSERM US24/CNRS UMS3633, Paris, France.

Marine Luka (M)

Laboratory of Inflammatory Responses and Transcriptomic Networks in Diseases, Université de Paris, Imagine Institute, INSERM UMR 1163, Paris, France.

Mickaël Ménager (M)

Laboratory of Inflammatory Responses and Transcriptomic Networks in Diseases, Université de Paris, Imagine Institute, INSERM UMR 1163, Paris, France.

Frédéric Relaix (F)

Univ Paris Est Creteil, INSERM, IMRB, Creteil, France.

Céline Colnot (C)

Univ Paris Est Creteil, INSERM, IMRB, Creteil, France. celine.colnot@inserm.fr.

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Classifications MeSH