Paul F. Glenn Laboratories for the Biology of Aging and Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA 94305, USA.
Dev Biol. 2013 Jul 15;379(2):195-207. doi: 10.1016/j.ydbio.2013.04.021. Epub 2013 Apr 29.
Myf5 is a member of the muscle-specific determination genes and plays a critical role in skeletal muscle development. Whereas the expression of Myf5 during embryonic and fetal myogenesis has been extensively studied, its expression in progenitors that will ultimately give rise to adult satellite cells, the stem cells responsible for muscle repair, is still largely unexplored. To investigate this aspect, we have generated a mouse strain carrying a CreER coding sequence in the Myf5 locus. In this strain, Tamoxifen-inducible Cre activity parallels endogenous Myf5 expression. Combining Myf5(CreER) and Cre reporter alleles, we were able to evaluate the contribution of cells expressing Myf5 at distinct developmental stages to the pool of satellite cells in adult hindlimb muscles. Although it was possible to trace back the origin of some rare satellite cells to a subpopulation of Myf5(+ve) progenitors in the limb buds at the late embryonic stage (∼E12), a significant number of satellite cells arise from cells which expressed Myf5 for the first time at the fetal stage (∼E15). These studies provide direct evidence that adult satellite cells derive from progenitors that first express the myogenic determination gene Myf5 during fetal stages of myogenesis.
Myf5 是肌肉特异性决定基因家族的成员,在骨骼肌发育中发挥着关键作用。虽然 Myf5 在胚胎期和胎儿期的成肌分化过程中的表达已经得到了广泛的研究,但它在最终产生成体卫星细胞(负责肌肉修复的干细胞)的前体细胞中的表达仍然在很大程度上未被探索。为了研究这一方面,我们构建了一个在 Myf5 基因座携带 CreER 编码序列的小鼠品系。在这个品系中,Tamoxifen 诱导的 Cre 活性与内源性 Myf5 表达平行。结合 Myf5(CreER)和 Cre 报告基因等位基因,我们能够评估在不同发育阶段表达 Myf5 的细胞对成年后肢肌肉卫星细胞池的贡献。虽然可以追溯到一些罕见的卫星细胞起源于胚胎晚期(约 E12)肢芽中一小部分 Myf5(+ve)前体细胞,但相当数量的卫星细胞来自于在胎儿期(约 E15)首次表达 Myf5 的细胞。这些研究提供了直接证据,表明成年卫星细胞来源于在成肌分化的胎儿阶段首次表达肌生成决定基因 Myf5 的前体细胞。