Borycki A G, Brunk B, Tajbakhsh S, Buckingham M, Chiang C, Emerson C P
Department of Cell Biology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104-6058, USA.
Development. 1999 Sep;126(18):4053-63. doi: 10.1242/dev.126.18.4053.
Sonic hedgehog (Shh), produced by the notochord and floor plate, is proposed to function as an inductive and trophic signal that controls somite and neural tube patterning and differentiation. To investigate Shh functions during somite myogenesis in the mouse embryo, we have analyzed the expression of the myogenic determination genes, Myf5 and MyoD, and other regulatory genes in somites of Shh null embryos and in explants of presomitic mesoderm from wild-type and Myf5 null embryos. Our findings establish that Shh has an essential inductive function in the early activation of the myogenic determination genes, Myf5 and MyoD, in the epaxial somite cells that give rise to the progenitors of the deep back muscles. Shh is not required for the activation of Myf5 and MyoD at any of the other sites of myogenesis in the mouse embryo, including the hypaxial dermomyotomal cells that give rise to the abdominal and body wall muscles, or the myogenic progenitor cells that form the limb and head muscles. Shh also functions in somites to establish and maintain the medio-lateral boundaries of epaxial and hypaxial gene expression. Myf5, and not MyoD, is the target of Shh signaling in the epaxial dermomyotome, as MyoD activation by recombinant Shh protein in presomitic mesoderm explants is defective in Myf5 null embryos. In further support of the inductive function of Shh in epaxial myogenesis, we show that Shh is not essential for the survival or the proliferation of epaxial myogenic progenitors. However, Shh is required specifically for the survival of sclerotomal cells in the ventral somite as well as for the survival of ventral and dorsal neural tube cells. We conclude, therefore, that Shh has multiple functions in the somite, including inductive functions in the activation of Myf5, leading to the determination of epaxial dermomyotomal cells to myogenesis, as well as trophic functions in the maintenance of cell survival in the sclerotome and adjacent neural tube.
由脊索和底板产生的音猬因子(Shh),被认为作为一种诱导和营养信号,控制体节和神经管的模式形成与分化。为了研究Shh在小鼠胚胎体节肌生成过程中的功能,我们分析了生肌决定基因Myf5和MyoD以及其他调控基因在Shh基因敲除胚胎的体节和来自野生型及Myf5基因敲除胚胎的前体节中胚层外植体中的表达情况。我们的研究结果表明,Shh在产生深层背部肌肉祖细胞的轴上体节细胞中,对生肌决定基因Myf5和MyoD的早期激活具有重要的诱导功能。在小鼠胚胎的任何其他肌生成部位,包括产生腹部和体壁肌肉的轴下体节皮肌细胞,或形成肢体和头部肌肉的生肌祖细胞,Myf5和MyoD的激活都不需要Shh。Shh在体节中还起到建立和维持轴上和轴下基因表达的中外侧边界的作用。在轴上的皮肌节中,Myf5而非MyoD是Shh信号传导的靶点,因为在前体节中胚层外植体中,重组Shh蛋白对MyoD的激活在Myf5基因敲除胚胎中存在缺陷。为了进一步支持Shh在轴上肌生成中的诱导功能,我们表明Shh对于轴上生肌祖细胞的存活或增殖并非必不可少。然而,Shh对于腹侧体节中硬骨细胞的存活以及腹侧和背侧神经管细胞的存活是特异性必需的。因此,我们得出结论,Shh在体节中具有多种功能,包括在激活Myf5方面的诱导功能,导致轴上的皮肌节细胞决定进行肌生成,以及在维持硬骨节和相邻神经管中细胞存活方面的营养功能。