Meola G
Istituto di Clinica Neurologica, Centro Dino Ferrari, Università degli Studi di Milano.
Ital J Neurol Sci. 1991 Jun;12(3):257-68. doi: 10.1007/BF02337773.
In this article I illustrated the use of regenerating human muscle cultures for studying the hereditary human myopathies. Although some of the data are still controversial, they do point up the great potential of this "in vitro system". For hereditary myopathies due to developmentally regulated proteins that are expressed only at a more advanced stage of muscle differentiation, the use of highly differentiated nerve-muscle cocultures might contribute significantly to a better understanding of their developmental pathogenesis. More advanced techniques (permanent human muscle cell lines, heterokaryons, myoblast transfer, gene transfer, myogenic conversion of human non-muscle cells, cybrid clones) may provide a great deal of information at molecular level and may also have practical applications in the diagnosis or even in the treatment of hereditary human myopathies.
在本文中,我阐述了利用再生的人类肌肉培养物来研究人类遗传性肌病。尽管一些数据仍存在争议,但它们确实凸显了这个“体外系统”的巨大潜力。对于由仅在肌肉分化更晚期阶段表达的发育调控蛋白引起的遗传性肌病,使用高度分化的神经 - 肌肉共培养物可能会极大地有助于更好地理解其发育发病机制。更先进的技术(永久性人类肌肉细胞系、异核体、成肌细胞转移、基因转移、人类非肌肉细胞的成肌转化、胞质杂种克隆)可能在分子水平上提供大量信息,并且在人类遗传性肌病的诊断甚至治疗中也可能有实际应用。