Abstract
MyoD mRNA is expressed in a subpopulation of cells within the embryonic epiblast. Most of these cells are incorporated into somites and synthesize Noggin. Ablation of MyoD-positive cells in the epiblast subsequently results in the herniation of organs through the ventral body wall, a decrease in the expression of Noggin, MyoD, Myf5, and myosin in the somites and limbs, and an increase in Pax-3-positive myogenic precursors. The addition of Noggin lateral to the somites compensates for the loss of MyoD-positive epiblast cells. Skeletal muscle stem cells that arise in the epiblast are utilized in the somites to promote muscle differentiation by serving as a source of Noggin. © The Rockefeller University Press.
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CITATION STYLE
Gerhart, J., Elder, J., Neely, C., Schure, J., Kvist, T., Knudsen, K., & George-Weinstein, M. (2006). MyoD-positive epiblast cells regulate skeletal muscle differentiation in the embryo. Journal of Cell Biology, 175(2), 283–292. https://doi.org/10.1083/jcb.200605037
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