p27(Kip1) acts downstream of n-cadherin-mediated cell adhesion to promote myogenesis beyond cell cycle regulation

摘要

It is widely acknowledged that cultured myoblasts can not differentiate at very low density. Here we analyzed the mechanism through which cell density influences myogenic differentiation in vitro. By comparing the behavior of C2C12 myoblasts at opposite cell densities, we found that, when cells are sparse, failure to undergo terminal differentiation is independent from cell cycle control and reflects the lack of p27(Kip1) and MyoD in proliferating myoblasts. We show that inhibition of p27(Kip1) expression impairs C2C12 cell differentiation at high density, while exogenous p27(Kip1) allows low-density cultured C2C12 cells to enter the differentiative program by regulating MyoD levels in undifferentiated myoblasts. We also demonstrate that the early induction of p27(Kip1) is a critical step of the N-cadherin-dependent signaling involved in myogenesis. Overall, our data support an active role of p27(Kip1) in the decision of myoblasts to commit to terminal differentiation, distinct from the regulation of cell proliferation, and identify a pathway that, reasonably, operates in vivo during myogenesis and might be part of the phenomenon known as "community effect".