Key result
Caspase-3 inhibition increases Pax7 protein ~2.5-fold in differentiating myoblasts, independent of proteasome degradation.
Why the study?
The regulation mechanisms controlling Pax7 protein levels during muscle precursor cell differentiation were not fully understood, particularly the roles of caspase-3 and proteasome activity.
Effect estimate: 2.45 fold increase
p-value: p=<0.01
Pax7 levels in early stages of muscle differentiation are regulated by at least two independent mechanisms involving caspase-3 and proteasome activity.
Pax7 proteasomal degradation may enable myoblast differentiation; leaves open in vivo validation and therapeutic translation.
The transcription factor Pax7 negatively regulates the activity of the muscle regulatory transcription factor MyoD, preventing muscle precursor cells from undergoing terminal differentiation. In this context, the ratio between Pax7 and MyoD protein levels is thought to be critical in allowing myogenesis to proceed or to maintain the undifferentiated muscle precursor state. We have previously shown that Pax7 is subject to rapid down regulation in differentiating myoblasts, via a proteasome-dependent pathway. Here we present evidence indicating that Pax7 is also subject to caspase-3-dependent regulation. Furthermore, simultaneous inhibition of caspase-3 and proteasome activity induced further accumulation of Pax7 protein in differentiating myoblasts. These results suggest that at early stages of muscle differentiation, Pax7 levels are regulated by at least two independent mechanisms involving caspase-3 and proteasome activity.
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Hugo C. Olguín (2011) studied Muscle differentiation. Caspase-3 and proteasome inhibition vs. Vehicle control was evaluated on Pax7 protein levels (2.45 fold increase, p=<0.01). Specific inhibition of caspase-3 activity resulted in a 2.45-fold accumulation of Pax7 protein in differentiating myoblasts, acting independently of proteasome-dependent degradation.
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