Cited by 267Muscle Physiology and DisordersNutrition and Health in AgingMitochondrial Function and Pathology

The DOI matches its Crossref record; 68 of the 68 references it cites were found in a registry or an index.

Genomic and Proteomic Profiling Reveals Reduced Mitochondrial Function and Disruption of the Neuromuscular Junction Driving Rat Sarcopenia

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Abstract

Molecular mechanisms underlying sarcopenia, the age-related loss of skeletal muscle mass and function, remain unclear. To identify molecular changes that correlated best with sarcopenia and might contribute to its pathogenesis, we determined global gene expression profiles in muscles of rats aged 6, 12, 18, 21, 24, and 27 months. These rats exhibit sarcopenia beginning at 21 months. Correlation of the gene expression versus muscle mass or age changes, and functional annotation analysis identified gene signatures of sarcopenia distinct from gene signatures of aging. Specifically, mitochondrial energy metabolism (e.g., tricarboxylic acid cycle and oxidative phosphorylation) pathway genes were the most downregulated and most significantly correlated with sarcopenia. Also, perturbed were genes/pathways associated with neuromuscular junction patency (providing molecular evidence of sarcopenia-related functional denervation and neuromuscular junction remodeling), protein degradation, and inflammation. Proteomic analysis of samples at 6, 18, and 27 months confirmed the depletion of mitochondrial energy metabolism proteins and neuromuscular junction proteins. Together, these findings suggest that therapeutic approaches that simultaneously stimulate mitochondrogenesis and reduce muscle proteolysis and inflammation have potential for treating sarcopenia.

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Metadata

Authors
Ibebunjo, C., Chick, J. M., Kendall, T., Eash, J. K., Li, C., Zhang, Y., Vickers, C., Wu, Z., Clarke, B. A., Shi, J., Cruz, J., Fournier, B., Brachat, S., Gutzwiller, S., Ma, Q., Markovits, J., Broome, M., Steinkrauss, M., Skuba, E., Galarneau, J.-R., Gygi, S. P., & Glass, D. J.
Affiliations
  • Muscle Diseases Group, Novartis Institutes for Biomedical Research, Cambridge, Massachusetts, USA
  • Harvard University (US)
  • Novartis Institutes for BioMedical Research (CH)
  • Cardiovascular and Metabolic Diseases, Novartis Institutes for Biomedical Research, Cambridge, Massachusetts, USA
  • Developmental and Molecular Pathways, Novartis Institutes for Biomedical Research, Cambridge, Massachusetts, USA
  • Preclinical Safety Sciences, Novartis Institutes for Biomedical Research, Cambridge, Massachusetts, USA
Venue
Molecular and Cellular Biology
Published
2013-01-01
Volume
33
Issue
2
Pages
194-212
ISSN
  • 0270-7306 (ISSN-L)
  • 1098-5549
OpenAlex
W2097103188
Cited by
267
References
68
Citations by year
2026: 5 · 2025: 11 · 2024: 18 · 2023: 22 · 2022: 15 · 2021: 30 · 2020: 23 · 2019: 30 · 2018: 22 · 2017: 20 · 2016: 25 · 2015: 20 · 2014: 20 · 2013: 6
FWCI
5.88
Type
journal article
Language
en
Open access
Locations
  • Molecular and Cellular Biology (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
  • Health Sciences › Medicine › Physiology (medical) › Nutrition and Health in Aging
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
Keywords
sarcopenia, skeletal muscle aging, mitochondrial bioenergetics, oxidative phosphorylation, TCA cycle, neuromuscular junction, muscle protein degradation, muscle inflammation, gene expression profiling, proteomic profiling, mitochondrial dysfunction, rat model
MeSH terms
Aging, Animals, DNA, Mitochondrial, Energy Metabolism, Immunohistochemistry, Male, Mitochondria, Neuromuscular Junction, Postmortem Changes, Signal Transduction, Up-Regulation, Linear Models, Rats, Sprague-Dawley, Muscle, Skeletal, Reverse Transcriptase Polymerase Chain Reaction, Proteome, Gene Expression Profiling, Proteomics, Microarray Analysis, Rats, Muscle Strength, Sarcopenia, Transcriptome

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