Maresin 1 repletion improves muscle regeneration after volumetric muscle loss

Author:

Castor-Macias Jesus A12ORCID,Larouche Jacqueline A12ORCID,Wallace Emily C1,Spence Bonnie D1,Eames Alec1,Duran Pamela12,Yang Benjamin A12,Fraczek Paula M12,Davis Carol A3,Brooks Susan V13,Maddipati Krishna Rao4,Markworth James F5ORCID,Aguilar Carlos A126ORCID

Affiliation:

1. Department of Biomedical Engineering, University of Michigan

2. Biointerfaces Institute, University of Michigan

3. Department of Molecular & Integrative Physiology, University of Michigan

4. Department of Pathology, Lipidomics Core Facility, Wayne State University

5. Department of Animal Sciences, Purdue University

6. Program in Cellular and Molecular Biology, University of Michigan

Abstract

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.

Funder

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Congressionally Directed Medical Research Programs

3M Foundation

American Federation for Aging Research

National Science Foundation

Defense Advanced Research Projects Agency

Hevolution Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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