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Fusion of dysfunction muscle stem cells with myofibers induces sarcopenia in mice
Xun Wang1, Prashant Mishra1,2,3
1Children's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390 USA.
Abstract:
Sarcopenia, or age-associated muscle atrophy, is a progressive condition which affects ~10-30% of the human geriatric population (1, 2). A number of contributors to sarcopenia have been proposed, including the progressive loss of muscle stem cells (MuSCs) with age. However, studies in mice have provided evidence that MuSC depletion is not sufficient to induce sarcopenia (3, 4). We recently showed that in response to age-associated mitochondrial damage, MuSCs self-remove by fusing with neighboring myofibers, which depletes the stem cell population of damaged progenitors (5). Here, we show that MuSC-myofiber fusion is sufficient to initiate myofiber atrophy in mice, which limits their motor function and lifespan. Conversely, inhibition of MuSC-myofiber fusion blocks myofiber atrophy with age, with a concomitant increase in the maximum lifespan of animals. These findings suggest a model where the accumulation fusion of damaged MuSCs with adult myofibers is a key driving feature of sarcopenia, and resolves the findings that MuSC depletion on its own does not initiate myofiber atrophy.
Insights
Age-associated muscle atrophy (sarcopenia) is driven by muscle stem cells (MuSCs) fusing with myofibers. Inhibiting this fusion prevents sarcopenia, extending lifespan.
Area of Science:
- Gerontology
- Muscle Biology
- Cellular Aging
Background:
- Sarcopenia, age-associated muscle atrophy, affects 10-30% of the elderly population.
- While muscle stem cell (MuSC) loss is implicated, it alone doesn't cause sarcopenia.
- Previous work showed MuSCs fuse with myofibers to remove damaged cells.
Approach:
- Investigated the functional consequences of MuSC-myofiber fusion in mice.
- Examined the effect of inhibiting MuSC-myofiber fusion on age-related muscle changes.
- Assessed impacts on motor function, lifespan, and myofiber atrophy.
Key Points:
- MuSC-myofiber fusion is sufficient to cause myofiber atrophy and reduce motor function and lifespan in mice.
- Inhibiting MuSC-myofiber fusion prevents age-related myofiber atrophy.
- Blocking this fusion significantly increases the maximum lifespan of animals.
Conclusions:
- MuSC-myofiber fusion is a key driver of sarcopenia, not just MuSC depletion.
- This fusion process contributes to age-related muscle decline and reduced lifespan.
- Targeting MuSC-myofiber fusion offers a potential therapeutic strategy for sarcopenia and longevity.
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