Maresin 1 repletion improves muscle regeneration after volumetric muscle loss.

immunology inflammation mouse regenerative medicine stem cells

Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
22 Dec 2023
Historique:
received: 26 01 2023
accepted: 21 12 2023
medline: 22 12 2023
pubmed: 22 12 2023
entrez: 22 12 2023
Statut: aheadofprint

Résumé

The acute traumatic or surgical loss of skeletal muscle, known as volumetric muscle loss (VML), is a devastating type of injury that results in exacerbated and persistent inflammation followed by fibrosis. The mechanisms that mediate the magnitude and duration of the inflammatory response and ensuing fibrosis after VML remain understudied and as such, the development of regenerative therapies has been limited. To address this need, we profiled how lipid mediators, which are potent regulators of the immune response after injury, varied with VML injuries that heal or result in fibrosis. We observed that non-healing VML injuries displayed increased pro-inflammatory eicosanoids and a lack of pro-resolving lipid mediators. Treatment of VML with a pro-resolving lipid mediator synthesized from docosahexaenoic acid, called Maresin 1, ameliorated fibrosis through reduction of neutrophils and macrophages and enhanced recovery of muscle strength. These results expand our knowledge of the dysregulated immune response that develops after VML and identify a novel immuno-regenerative therapeutic modality in Maresin 1.

Identifiants

pubmed: 38131691
doi: 10.7554/eLife.86437
pii: 86437
doi:
pii:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIAMS NIH HHS
ID : P30 AR069620
Pays : United States

Informations de copyright

© 2023, Castor-Macias et al.

Déclaration de conflit d'intérêts

JC, JL, EW, BS, AE, PD, BY, PF, CD, SB, KM, JM, CA The authors declare that no competing interests exist.

Auteurs

Jesus A Castor-Macias (JA)

Department of Biomedical Engineering, University of Michigan-Ann Arbor, Ann Arbor, United States.

Jacqueline A Larouche (JA)

Department of Biomedical Engineering, University of Michigan-Ann Arbor, Ann Arbor, United States.

Emily C Wallace (EC)

Department of Biomedical Engineering, University of Michigan-Ann Arbor, Ann Arbor, United States.

Bonnie D Spence (BD)

Department of Biomedical Engineering, University of Michigan-Ann Arbor, Ann Arbor, United States.

Alec Eames (A)

Department of Biomedical Engineering, University of Michigan-Ann Arbor, Ann Arbor, United States.

Pamela Duran (P)

Department of Biomedical Engineering, University of Michigan-Ann Arbor, Ann Arbor, United States.

Benjamin A Yang (BA)

Department of Biomedical Engineering, University of Michigan-Ann Arbor, Ann Arbor, United States.

Paula M Fraczek (PM)

Department of Biomedical Engineering, University of Michigan-Ann Arbor, Ann Arbor, United States.

Carol A Davis (CA)

Department of Molecular and Integrative Physiology, University of Michigan-Ann Arbor, Ann Arbor, United States.

Susan V Brooks (SV)

Department of Biomedical Engineering, University of Michigan-Ann Arbor, Ann Arbor, United States.

Krishna Rao Maddipati (KR)

Department of Pathology, Wayne State University, Detroit, United States.

James F Markworth (JF)

Department of Animal Sciences, Purdue University West Lafayette, West Lafayette, United States.

Carlos A Aguilar (CA)

Department of Biomedical Engineering, University of Michigan-Ann Arbor, Ann Arbor, United States.

Classifications MeSH