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首页> 外文期刊>Biology Bulletin >Analysis of Expression of Heavy Myosin Chains during in vitro Differentiation of Satellite Cells and Myoblasts Derived from Rat Skeletal Muscles
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Analysis of Expression of Heavy Myosin Chains during in vitro Differentiation of Satellite Cells and Myoblasts Derived from Rat Skeletal Muscles

机译:大鼠骨骼肌来源卫星细胞和成肌细胞体外分化过程中重肌球蛋白链表达的分析

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Differentiation of cultured myogenic progenitor cells (satellite cells and mononucleated myoblasts) derived from hindlimb muscles of rat embryos and newborn animals was studied. Immunocytochemical methods and PCR analysis revealed expression of heavy myosin chains at the earliest stages of myogenesis (in mononucleated myoblasts). Expression of the gene encoding the embryonic form of myosin and a low level of expression of the gene encoding perinatal myosin in cultured progenitor cells derived from embryonic muscles was detected by PCR. Cells derived from muscles of newborn animals also expressed these two myosin forms, though at a lower level. The progenitor cells derived from muscles of rat embryos and newborn animals were found to express myosin 2a, which is characteristic of fast-twitch definitive muscle fibers.
机译:研究了源自大鼠胚胎和新生动物后肢肌肉的培养的成肌祖细胞(卫星细胞和单核成肌细胞)的分化。免疫细胞化学方法和PCR分析表明,在肌生成的最早阶段(在单核成肌细胞中),表达了重的肌球蛋白链。通过PCR检测在培养的源自胚胎肌肉的祖细胞中编码肌球蛋白的胚胎形式的基因的表达和围产期肌球蛋白的基因的低水平表达。新生动物肌肉细胞也表达了这两种肌球蛋白形式,尽管含量较低。发现源自大鼠胚胎和新生动物的肌肉的祖细胞表达肌球蛋白2a,这是快速抽动的最终肌纤维的特征。

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  • 来源
    《Biology Bulletin 》 |2009年第3期| 213-219| 共7页
  • 作者单位

    Kol'tsov Institute of Developmental Biology, Russian Academy of Sciences, ul. Vavilova 26, Moscow, 119991 Russia;

    Kol'tsov Institute of Developmental Biology, Russian Academy of Sciences, ul. Vavilova 26, Moscow, 119991 Russia;

    Kol'tsov Institute of Developmental Biology, Russian Academy of Sciences, ul. Vavilova 26, Moscow, 119991 Russia;

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