Loss of adult skeletal muscle stem cells drives age-related neuromuscular junction degeneration

Author:

Liu Wenxuan12,Klose Alanna1,Forman Sophie3,Paris Nicole D1ORCID,Wei-LaPierre Lan4,Cortés-Lopéz Mariela5,Tan Aidi67,Flaherty Morgan2,Miura Pedro5,Dirksen Robert T4,Chakkalakal Joe V189ORCID

Affiliation:

1. Department of Orthopaedics and Rehabilitation, Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, United States

2. Department of Biomedical Genetics, University of Rochester Medical Center, Rochester, United States

3. Department of Biology, University of Rochester, Rochester, United States

4. Department of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, United States

5. Department of Biology, University of Nevada, Reno, United States

6. Bioinformatics Division and Center for Synthetic and Systems Biology, Tsinghua University, Beijing, China

7. TNLIST/Department of Automation, Tsinghua University, Beijing, China

8. Stem Cell and Regenerative Medicine Institute, University of Rochester Medical Center, Rochester, United States

9. The Rochester Aging Research Center, University of Rochester Medical Center, Rochester, United States

Abstract

Neuromuscular junction degeneration is a prominent aspect of sarcopenia, the age-associated loss of skeletal muscle integrity. Previously, we showed that muscle stem cells activate and contribute to mouse neuromuscular junction regeneration in response to denervation (Liu et al., 2015). Here, we examined gene expression profiles and neuromuscular junction integrity in aged mouse muscles, and unexpectedly found limited denervation despite a high level of degenerated neuromuscular junctions. Instead, degenerated neuromuscular junctions were associated with reduced contribution from muscle stem cells. Indeed, muscle stem cell depletion was sufficient to induce neuromuscular junction degeneration at a younger age. Conversely, prevention of muscle stem cell and derived myonuclei loss was associated with attenuation of age-related neuromuscular junction degeneration, muscle atrophy, and the promotion of aged muscle force generation. Our observations demonstrate that deficiencies in muscle stem cell fate and post-synaptic myogenesis provide a cellular basis for age-related neuromuscular junction degeneration and associated skeletal muscle decline.

Funder

National Institute on Aging

Congressionally Directed Medical Research Programs

New York Stem Cell 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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