Regeneration of muscle fibers after myoblast injection into dystrophic muscle
Regeneration of muscle fibers after myoblast injection into dystrophic muscle
批准号:
05557001
负责人:
SHIMADA Yutaka
金额:
$5.25万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Developmental Scientific Research (B)
财政年份:
1993
资助国家:
日本
项目状态:
已结题
起止时间:
1993 至 1995
中文摘要
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英文摘要
1. Muscle regeneration : Muscle regeneration was evoked by a cold injury on the surface of slow (the anterior latissimus dorsi) and fast (the posterior latissimus dorsi) muscles of adult chickens. In the fibers with nerves intact, troponin was expressed 1 day earlier than dystrophin and changed to its adult isoform more than 2 weeks after the stage when dystrophin exhibited the same appearance as that in normal fibers. Further, although regenerating fibers in denervated muscle switched on the expression of troponin similarly to those in innervated muscle, many of them again reverted to an embryonic state. However, no difference was found in the dystrophin expression between regenerating fibers with nerves intact and those with nerves resected. These results indicate that the expression of troponin and dystrophin genes is regulated independently during regeneration and that nerves are required for the full development of the former protein while unnecessary for the latter.2. Culture of dissociated myoblasts : Microinjection of actin an myosin into cardiomyocytes in vitro revealed that incorporation of these monomeric proteins occurred preferentially at immature portions of developing myofibrils, where connectin was distributed faintly and uniformly. It seems that polymerization of actin and/or the addition of newly formed actin filaments occur in assoiation with myosin filaments in myofibrils and these of myosin arise from the A-I junctional regions of myofibrils.3. Muscle fiber formation after C2 cell injection : PKH26-labelled C2 cells were injected into the tibialis anterior muscle of mice (ScN and mdx). These transferred C2 cells were seen to fuse with myoblasts of the host muscle fibers and formed chimera fibers. This method will be useful for further basic investigations of gene therapy of genetic muscle diseases.
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Katsunori.Kouchi: "Incorporation of microinjected biotin-labelled actin into nascent myofibrils of cardiac myocytes:an immunoelectron microscopic study." Journal of Muscle Research and Cell Motility. 14. 292-301 (1993)
Katsunori.Kouchi:“将显微注射的生物素标记的肌动蛋白掺入心肌细胞的新生肌原纤维中:一项免疫电子显微镜研究。”
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作者:
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通讯作者:
Yutaka Shimada: "Distribution of connectin (titin) and transverse-tubules at myotendinous junctions." Scanning Microscopy. 7. 157-163 (1993)
Yutaka Shimada:“连接蛋白(肌联蛋白)和横管在肌腱连接处的分布。”
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Fujio Atsuta: "Distribution of connectin(titin),nebulin and α-actinin at myotendinous junctions of chicken pectoralis muscles: an immunofluorescence and immunoelectron microscopic study." Journal of Muscle Research and Cell Motility. 14. 511-517 (1993)
Fujio Atsuta:“连接蛋白(肌联蛋白)、星云蛋白和 α-肌动蛋白在鸡胸肌肌腱连接处的分布:免疫荧光和免疫电子显微镜研究。”肌肉研究和细胞运动杂志 14. 511-517 (1993)。
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Yutaka Shimada: "Development of connectin/titin and nebulin in striated muscles of chicken." Advances in Biophysics. (印刷中).
Yutaka Shimada:“鸡横纹肌中连接蛋白/肌联蛋白和星云蛋白的发展”(生物物理学进展)。
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Masatoshi Komiyama: "Troponin and dystrophin in regenerating muscle fibers with and without denervation." Muscle & Nerve. 17. 1062-1064 (1994)
Masatoshi Komiyama:“肌钙蛋白和肌营养不良蛋白在去神经和不去神经的情况下再生肌纤维中的作用。”
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