Murray B, Wilson D J
School of Clinical Dentistry, Queen's University of Belfast, Northern Ireland, UK.
J Anat. 1997 Feb;190 ( Pt 2)(Pt 2):261-73. doi: 10.1046/j.1469-7580.1997.19020261.x.
Adult muscle is highly vascularised, with blood vessels being essential for adequate oxygenation of the tissue and for supporting increased metabolic demands. Whether this is the case during muscle development has not been examined. Resin histology was used to map the muscle splitting process and conventional transmission electron microscopy to examine early muscle differentiation at the midlimb level or later at the mid radius/ulna level in the chick wing bud from stages 24 (4.5 d) to 36 (10 d) (Hamburger & Hamilton, 1951). Microinjection of India Ink into the extra-embryonic vasculature was used to visualise the patent muscle microcirculation. The results showed that the premuscle masses are present at stage 24 and initial splitting of the muscle masses commences at stage 28. The final muscle pattern is not established until stage 36. At stage 26 the cells within the premuscle masses exhibited a mesenchymal morphology, but at stage 28 overt muscle differentiation was evident with myofibrils present within myoblasts. Undifferentiated mononucleated cells were interspersed with the differentiating myoblasts. The ratio of mononucleated cells:myoblasts decreased and the myoblasts became plumper and increasingly packed with myofibrils with age. There was no evidence of secondary myotube formation at any of the stages examined. Vascular invasion of the limb occurred at stage 35 just prior to the establishment of the final muscle pattern. This was surprising as it was assumed that myogenic differentiation would be both oxygen and nutrient dependent. The results of this study provide descriptions of the splitting of the premuscle masses through to the establishment of the final muscle pattern at the midlimb or mid radius/ulna level of the chick wing bud together with the differentiation of the myogenic cells within the developing muscles. However, the relationship between muscle patterning at the tissue level and muscle differentiation at the cellular level with vascularisation remains unclear. It is hoped that the results of the study may provide the basis for future investigations into mechanisms involved in muscle patterning and the signalling mechanisms for vascular invasion.
成年肌肉血管高度丰富,血管对于组织的充分氧合以及满足增加的代谢需求至关重要。在肌肉发育过程中是否如此尚未得到研究。采用树脂组织学来描绘肌肉分裂过程,并使用传统透射电子显微镜检查鸡胚翅芽在第24阶段(4.5天)至第36阶段(10天)中肢水平早期或稍后尺骨/桡骨中段水平的肌肉早期分化情况(Hamburger和Hamilton,1951)。将印度墨汁显微注射到胚外血管系统中以观察开放的肌肉微循环。结果显示,在第24阶段存在肌原基,肌肉团块的初始分裂在第28阶段开始。直到第36阶段才建立最终的肌肉模式。在第26阶段,肌原基内的细胞呈现间充质形态,但在第28阶段,明显的肌肉分化可见,成肌细胞内出现肌原纤维。未分化的单核细胞散布在分化的成肌细胞之间。随着年龄增长,单核细胞与成肌细胞的比例下降,成肌细胞变得更饱满,肌原纤维越来越多。在所检查的任何阶段均未发现二次肌管形成的证据。在最终肌肉模式建立之前的第35阶段,肢体发生血管侵入。这令人惊讶,因为人们认为肌源性分化将依赖于氧气和营养物质。本研究结果描述了鸡胚翅芽中肢或尺骨/桡骨中段水平从肌原基分裂到最终肌肉模式建立的过程,以及发育中肌肉内肌源性细胞的分化情况。然而,组织水平的肌肉模式形成与细胞水平的肌肉分化与血管形成之间的关系仍不清楚。希望该研究结果可为未来研究肌肉模式形成机制及血管侵入的信号传导机制提供基础。