Guo Y, Dorn T, Kuehl SJ, Linnemann A, Rothe M, Pfister AS, Vainio S, Laugwitz KL, Moretti A, Kuehl M (2019)
Publication Type: Journal article
Publication year: 2019
Book Volume: 449
Pages Range: 1-13
Journal Issue: 1
DOI: 10.1016/j.ydbio.2019.02.009
Wnt proteins can activate different intracellular signaling pathways. These pathways need to be tightly regulated for proper cardiogenesis. The canonical Wnt/β-catenin inhibitor Dkk1 has been shown to be sufficient to trigger cardiogenesis in gain-of-function experiments performed in multiple model systems. Loss-of-function studies however did not reveal any fundamental function for Dkk1 during cardiogenesis. Using Xenopus laevis as a model we here show for the first time that Dkk1 is required for proper differentiation of cardiomyocytes, whereas specification of cardiomyocytes remains unaffected in absence of Dkk1. This effect is at least in part mediated through regulation of non-canonical Wnt signaling via Wnt11. In line with these observations we also found that Isl1, a critical regulator for specification of the common cardiac progenitor cell (CPC) population, acts upstream of Dkk1.
APA:
Guo, Y., Dorn, T., Kuehl, S.J., Linnemann, A., Rothe, M., Pfister, A.S.,... Kuehl, M. (2019). The Wnt inhibitor Dkk1 is required for maintaining the normal cardiac differentiation program in Xenopus laevis. Developmental Biology, 449(1), 1-13. https://doi.org/10.1016/j.ydbio.2019.02.009
MLA:
Guo, Yanchun, et al. "The Wnt inhibitor Dkk1 is required for maintaining the normal cardiac differentiation program in Xenopus laevis." Developmental Biology 449.1 (2019): 1-13.
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