The MRL/MpJ Mouse Strain Is Not Protected From Muscle Atrophy and Weakness After Rotator Cuff Tear

Jeffrey R. Talarek, Alex N. Piacentini, Alexis C. Konja, Susumu Wada, Jacob B. Swanson, Samuel C. Nussenzweig, Joshua S. Dines, Scott A. Rodeo, Christopher L. Mendias

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

Chronic rotator cuff tears are a common source of shoulder pain and disability. Patients with rotator cuff tears often have substantial weakness, fibrosis, and fat accumulation, which limit successful surgical repair and postoperative rehabilitation. The Murphy Roths Large (MRL) strain of mice have demonstrated superior healing and protection against pathological changes in several disease and injury conditions. We tested the hypothesis that, compared with the commonly used C57Bl/6 (B6) strain, MRL mice would have less muscle fiber atrophy and fat accumulation, and be protected against the loss in force production that occurs after cuff tear. Adult male B6 and MRL mice were subjected to a rotator cuff tear, and changes in muscle fiber contractility and histology were measured. RNA sequencing and shotgun metabolomics and lipidomics were also performed. The muscles were harvested one month after tear. B6 and MRL mice had a 40% reduction in relative muscle force production after rotator cuff tear. RNA sequencing identified an increase in fibrosis-associated genes and a reduction in mitochondrial metabolism genes. The markers of glycolytic metabolism increased in B6 mice, while MRL mice appeared to increase amino acid metabolism after tear. There was an accumulation of lipid after injury, although there was a divergent response between B6 and MRL mice in the types of lipid species that accrued. There were strain-specific differences between the transcriptome, metabolome, and lipidome of B6 and MRL mice, but these differences did not protect MRL mice from weakness and pathological changes after rotator cuff tear.

Original languageEnglish
Pages (from-to)811-822
Number of pages12
JournalJournal of Orthopaedic Research
Volume38
Issue number4
DOIs
Publication statusPublished - Apr 1 2020

Bibliographical note

Publisher Copyright:
© 2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc.

Funding

The University of Michigan Metabolomics Core is supported by NIH grant U24‐DK097153. Bioinformatics support was provided by a grant from the Tow Foundation for the David Z. Rosensweig Genomics Center at the Hospital for Special Surgery. We would like to acknowledge technical assistance from Dr. David Oliver and Mr. Damonie Salmon at the Hospital for Special Surgery.

FundersFunder number
National Institutes of HealthU24‐DK097153
National Institute of Arthritis and Musculoskeletal and Skin DiseasesR01AR063649
Center for Outcomes Research and Evaluation, Yale School of Medicine
University of Michigan
Tow Foundation

    ASJC Scopus Subject Areas

    • Orthopedics and Sports Medicine

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