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首页> 外文期刊>Free Radical Biology and Medicine: The Official Journal of the Oxygen Society >Advanced age-related denervation and fiber-type grouping in skeletal muscle of SOD1 knockout mice.
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Advanced age-related denervation and fiber-type grouping in skeletal muscle of SOD1 knockout mice.

机译:SOD1基因敲除小鼠骨骼肌中与年龄相关的晚期神经支配和纤维类型分组。

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In this study skeletal muscles from 1.5- and 10-month-old Cu/Zn superoxide dismutase (SOD1) homozygous knockout (JLSod1(-/-)) mice obtained from The Jackson Laboratory (C57Bl6/129SvEv background) were compared with muscles from age- and sex-matched heterozygous (JLSod1(+/-)) littermates. The results of this study were compared with previously published data on two different strains of Sod1(-/-) mice: one from Dr. Epstein's laboratory (ELSod1(-/-); C57Bl6 background) and the other from Cephalon, Inc. (CSod1(-/-); 129/CD-1 background). Grouping of succinate dehydrogenase-positive fibers characterized muscles of Sod1(-/-) mice from all three strains. The 10-month-old Sod1(-/-)C and JL mice displayed pronounced denervation of the gastrocnemius muscle, whereas the ELSod1(-/-) mice displayed a small degree of denervation at this age, but developed accelerated age-related denervation later on. Denervation markers were up-regulated in skeletal muscle of 10-month-old JLSod1(-/-) mice. This study is the first to show that metallothionein mRNA and protein expression was up-regulated in the skeletal muscle of 10-month-old JLSod1(-/-) mice and was mostly localized to the small atrophic muscle fibers. In conclusion, all three strains of Sod1(-/-) mice develop accelerated age-related muscle denervation, but the genetic background has significant influence on the progress of denervation.
机译:在这项研究中,将来自杰克逊实验室(C57Bl6 / 129SvEv)的1.5个月和10个月大的纯铜/锌超氧化物歧化酶(SOD1)纯合敲除(JLSod1(-/-))小鼠的骨骼肌与年龄相比较的肌肉进行了比较。 -和性别匹配的杂合子(JLSod1(+/-))同窝仔。这项研究的结果与先前发表的关于两种不同Sod1(-/-)小鼠品系的数据进行了比较:一种来自爱泼斯坦博士实验室(ELSod1(-/-); C57Bl6背景),另一种来自Cephalon,Inc.( CSod1(-/-); 129 / CD-1背景)。琥珀酸脱氢酶阳性纤维的分组表征了来自所有三个品系的Sod1(-/-)小鼠的肌肉。 10个月大的Sod1(-/-)C和JL小鼠表现出腓肠肌的明显失神经,而ELSod1(-/-)小鼠在该年龄表现出较小的失神经,但发展了与年龄相关的加速失神经稍后的。在10个月大的JLSod1(-/-)小鼠的骨骼肌中去神经标记物被上调。这项研究是第一个显示金属硫蛋白mRNA和蛋白质表达在10个月大的JLSod1(-/-)小鼠的骨骼肌中上调的结构,并且主要定位于萎缩的小肌纤维。总之,所有三株Sod1(-/-)小鼠均出现与年龄相关的加速肌肉神经支配,但是遗传背景对神经支配的进展有重要影响。

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