First published online November 27, 2006
Journal of Cell Science 119, 2301e (2006)
© The Company of Biologists Limited
Myogenesis: making contact and giving the right signals
Cell-cell contacts are important during development in part because they initiate signals that regulate differentiation. During myogenesis, the formation of cadherin-based adhesions between committed but proliferating myoblasts triggers their exit from the cell cycle and terminal differentiation. Now, Jennifer Pell and co-workers report that cadherin-mediated activation of the small GTPase RhoA and p38 MAP kinase (p38 MAPK) links the formation of cell-cell contacts to the synthesis of the pro-myogenic growth factor IGF-II (see p. 4828). p38 MAPK is essential for myogenesis but what regulates its activity during this process had remained unclear. The authors first noticed a correlation between the initial density of mouse myoblasts and N-cadherin levels, p38 MAPK phosphorylation, Igf2 expression and myogenesis. They then used N-cadherin, dominant-negative N-cadherin, constitutively active and dominant-negative forms of RhoA, and p38 MAPK constructs to investigate how cell-cell adhesion is linked to myogenesis. They conclude that N-cadherin activation through cell-cell contact activates RhoA. This then activates the
- and ß-isoforms of p38 MAPK, which in turn stimulates IGF-II synthesis and myogenesis.

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- Convergence of Igf2 expression and adhesion signalling via RhoA and p38 MAPK enhances myogenic differentiation
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JCS 2006 119: 4828-4840.
[Abstract]
[Full Text]