Buffinger N, Stockdale F E
Stanford University, School of Medicine, CA 94305-5306.
Development. 1994 Jun;120(6):1443-52. doi: 10.1242/dev.120.6.1443.
Specification of the myogenic phenotype in somites was examined in the early chick embryo using organotypic explant cultures stained with monoclonal antibodies to myosin heavy chain. It was found that myogenic specification (formation of muscle fibers in explants of somites or segmental plates cultured alone) does not occur until Hamburger and Hamilton stage 11 (12-14 somites). At this stage, only the somites in the rostral half of the embryo are myogenically specified. By Hamburger and Hamilton stage 12 (15-17 somites), the three most caudal somites were not specified to be myogenic while most or all of the more rostral somites are specified to myogenesis. Somites from older embryos (stage 13-15, 18-26 somites) showed the same pattern of myogenic specification--all but the three most caudal somites were specified. We investigated the effects of the axial structures, the notochord and neural tube, on myogenic specification. Both the notochord and neural tube were able to induce myogenesis in unspecified somites. In contrast, the neural tube, but not the notochord, was able to induce myogenesis in explants of segmental plate, a structure which is not myogenic when cultured alone. When explants of specified somites were stained with antibodies to slow or fast MyHC, it was found that myofiber diversity (fast and fast slow fibers) was established very early in development (as early as Hamburger and Hamilton stage 11). We also found fiber diversity in explants of unspecified somites (the three most caudal somites from stage 11 to 15) when they were recombined with notochord or neural tube. We conclude that myogenic specification in the embryo results in diverse fiber types and is an inductive process which is mediated by factors produced by the neural tube and notochord.
利用抗肌球蛋白重链单克隆抗体染色的器官型外植体培养技术,在早期鸡胚中研究了体节中肌源性表型的特化情况。研究发现,肌源性特化(单独培养的体节或节段板外植体中肌纤维的形成)直到汉伯格和汉密尔顿第11阶段(12 - 14个体节)才会发生。在此阶段,只有胚胎头侧一半的体节发生了肌源性特化。到汉伯格和汉密尔顿第12阶段(15 - 17个体节)时,最尾端的三个体节未被特化为肌源性,而大多数或所有更靠前的体节则被特化为肌生成。来自较老胚胎(第13 - 15阶段,18 - 26个体节)的体节呈现出相同的肌源性特化模式——除了最尾端的三个体节外,其余均被特化。我们研究了轴向结构,即脊索和神经管,对肌源性特化的影响。脊索和神经管都能够在未特化的体节中诱导肌生成。相比之下,神经管而非脊索能够在节段板外植体中诱导肌生成,节段板单独培养时不是肌源性结构。当用抗慢或快肌球蛋白重链(MyHC)抗体对特化体节的外植体进行染色时,发现肌纤维多样性(快肌纤维和快慢肌纤维)在发育早期(早在汉伯格和汉密尔顿第11阶段)就已确立。我们还发现,当未特化体节(第11至15阶段最尾端的三个体节)的外植体与脊索或神经管重组时,也存在纤维多样性。我们得出结论,胚胎中的肌源性特化导致了多种纤维类型的产生,并且是一个由神经管和脊索产生的因子介导的诱导过程。