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1 Department of Pharmacology and 2 Graduate Program in Biochemistry, Cell and Developmental Biology, Emory University, Atlanta, Georgia 30322
Slow-twitch skeletal muscle atrophies greatly in
response to unloading conditions. The cellular mechanisms that
contribute to the restoration of muscle mass after atrophy are largely
unknown. Here, we show that atrophy of the mouse soleus is associated
with a 36% decrease in myonuclear number after 2 wk of hindlimb
suspension. Myonuclear number is restored to control values during the
2-wk recovery period in which muscle mass returns to normal, suggesting that muscle precursor cells proliferate and fuse with myofibers. Inhibition of muscle precursor cell proliferation by local
-irradiation of the hindlimb completely prevents this increase in
myonuclear number. Muscle growth occurs normally during the first week
in irradiated muscles, but growth during the second week is inhibited, leading to a 50% attenuation in the restoration of muscle mass. Thus
early muscle growth occurs independently of an increase in myonuclear
number, whereas later growth requires proliferating muscle precursor
cells leading to myonuclear accretion. These results suggest that
increasing the proliferative capacity of muscle precursor cells may
enhance restoration of muscle mass after atrophy.
hindlimb suspension; gamma-irradiation; myonuclear number; satellite cells; soleus
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