Gensch Nicole, Borchardt Thilo, Schneider Andre, Riethmacher Dieter, Braun Thomas
Max-Planck-Institute for Heart and Lung Research, Parkstr. 1, 61231 Bad Nauheim, Germany.
Development. 2008 May;135(9):1597-604. doi: 10.1242/dev.019331. Epub 2008 Mar 26.
The development of myogenic cells is mainly determined by expression of two myogenic factors, Myf5 and Myod1 (MyoD), which genetically compensate for each other during embryogenesis. Here, we demonstrate by conditional cell ablation in mice that Myf5 determines a distinct myogenic cell population, which also contains some Myod1-positive cells. Ablation of this lineage uncovers the presence of a second autonomous myogenic lineage, which superseded Myf5-dependent myogenic cells and expressed Myod1. By contrast, ablation of myogenin-expressing cells erased virtually all differentiated muscle cells, indicating that some aspects of the myogenic program are shared by most skeletal muscle cells. We conclude that Myf5 and Myod1 define different cell lineages with distinct contributions to muscle precursor cells and differentiated myotubes. Individual myogenic cell lineages seem to substitute for each other within the developing embryo.
生肌细胞的发育主要由两种生肌因子Myf5和Myod1(MyoD)的表达所决定,它们在胚胎发生过程中在基因上相互补偿。在此,我们通过对小鼠进行条件性细胞消融证明,Myf5决定了一个独特的生肌细胞群体,其中也包含一些Myod1阳性细胞。消除这个谱系揭示了第二个自主生肌谱系的存在,它取代了Myf5依赖性生肌细胞并表达Myod1。相比之下,消除表达生肌调节因子的细胞几乎消除了所有分化的肌肉细胞,这表明生肌程序的某些方面为大多数骨骼肌细胞所共有。我们得出结论,Myf5和Myod1定义了不同的细胞谱系,它们对肌肉前体细胞和分化的肌管有不同的贡献。在发育中的胚胎内,各个生肌细胞谱系似乎可以相互替代。