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Muscle as a “Mediator” of Systemic Metabolism
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Skeletal and cardiac muscles play key roles in the regulation of systemic energy homeostasis and display remarkable plasticity in their metabolic responses to caloric availability and physical activity. In this Perspective we discuss recent studies highlighting transcriptional mechanisms that govern systemic metabolism by striated muscles. We focus on the participation of the Mediator complex in this process, and suggest that tissue-specific regulation of Mediator subunits impacts metabolic homeostasis.
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“Consistently, the metabolic adaptations occurring in skeletal muscles are assumed to work as a disease modifier and the quality of muscle mass is an important predictor of mortality1.”
From Mechanisms of muscle atrophy and hypertrophy: implications in health and disease (2021) · cites this paper as [1]
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“Being the most abundant tissue (40–50% of the total mass in healthy-weight individual) and the protein reservoir in the human body, skeletal muscles not only control locomotion but they are fundamental for breathing, eating, energy expenditure, as well as for glucose, amino acids, and lipids homeostasis and for maintaining a high quality of life1.”
From Mechanisms of muscle atrophy and hypertrophy: implications in health and disease (2021) · cites this paper as [1]
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Metadata
- Authors
- Baskin, K. K., Winders, B. R., & Olson, E. N.
- Affiliations
- The University of Texas Southwestern Medical Center (US)
- Corresponding author
- Olson, Eric N.
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2015-02
- Volume
- 21
- Issue
- 2
- Pages
- 237-248
- ISSN
- 1550-4131 (ISSN-L)
- PMC
- PMC4398026
- OpenAlex
- W2052045659
- Cited by
- 333
- References
- 139
- Citations by year
- 2026: 38 · 2025: 38 · 2024: 47 · 2023: 41 · 2022: 42 · 2021: 43 · 2020: 25 · 2019: 17 · 2018: 10 · 2017: 14 · 2016: 10 · 2015: 7
- FWCI
- 1.32
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (5u01hl100401-07)
- National Heart, Lung, and Blood Institute (R01HL111665, R01HL077439, HL- 111665, U01-HL-100401, R01HL053351, R01HL093039, HL077439, HL093039)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK099653, R01DK099653)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Health Sciences › Medicine › Physiology (medical) › Adipose Tissue and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Keywords
- Mediator complex, skeletal muscle, myocardium, muscle metabolism, transcriptional regulation, tissue-specific gene regulation, physical activity, metabolic plasticity
- MeSH terms
- Animals, Energy Metabolism, Homeostasis, Humans, Muscles
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