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BMP signaling regulates Nkx2-5 activity during cardiomyogenesis

Nkx2-5 regulates the transcription of muscle-specific genes during cardiomyogenesis. Nkx2-5 expression can induce cardiomyogenesis in aggregated P19 cells but not in monolayer cultures. In order to investigate the mechanism by which cellular aggregation regulates Nkx2-5 function, we examined the rol...

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Bibliographic Details
Published in:FEBS letters 2001-11, Vol.509 (1), p.126-130
Main Authors: Jamali, Mina, Karamboulas, Christina, Rogerson, Parker J, Skerjanc, Ilona S
Format: Article
Language:English
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Summary:Nkx2-5 regulates the transcription of muscle-specific genes during cardiomyogenesis. Nkx2-5 expression can induce cardiomyogenesis in aggregated P19 cells but not in monolayer cultures. In order to investigate the mechanism by which cellular aggregation regulates Nkx2-5 function, we examined the role of bone morphogenetic protein 4 (BMP4). We showed that the expression of the BMP inhibitor, noggin, was sufficient to inhibit the induction of cardiomyogenesis by Nkx2-5 during cellular aggregation. Furthermore, soluble BMP4 could activate Nkx2-5 function in monolayer cultures, resulting in the formation of cardiomyocytes. Therefore, BMP signaling is necessary and sufficient for the regulation of Nkx2-5 activity during cardiomyogenesis in P19 cells.
ISSN:0014-5793
1873-3468
DOI:10.1016/S0014-5793(01)03151-9