首页> 外文期刊>Toxicology and Applied Pharmacology >Metallothionein and apoptosis during differentiation of myoblasts to myotubes: protection against free radical toxicity.
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Metallothionein and apoptosis during differentiation of myoblasts to myotubes: protection against free radical toxicity.

机译:成肌细胞分化为肌管过程中的金属硫蛋白和凋亡:针对自由基毒性的保护。

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摘要

The changes in subcellular localization of metallothionein (MT) during differentiation were studied in two muscle cell lines, L6 and H9C2, myoblasts in order to understand the nuclear presence of MT and its antiapoptotic property. In myoblasts, MT and zinc were localized mainly in the cytoplasm but were translocated into the nucleus of newly formed myotubes during early stage of differentiation, which was initiated by lowering FBS from 10% to 1%. In fully differentiated myotubes, metallothionein content was decreased with a cytoplasmic localization. These changes in subcellular localization of MT and Zn were accompanied by increased apoptosis in myotubes. The changes in the apoptosis at different stages of differentiation were measured by both DNA ladder formation and TUNEL technique. The results also show that the apoptosis may be initiated by free radical generation and may be accompanied by p53 expression. The H9C2 cells contained high levels of MT, differentiated slowly, and had low incidence of apoptotic bodies compared to L6 cell line. Copyright 1999 Academic Press.
机译:为了了解MT的核存在及其抗凋亡特性,在两个肌肉细胞系L6和H9C2成肌细胞中研究了金属硫蛋白(MT)在分化过程中亚细胞定位的变化。在成肌细胞中,MT和锌主要定位在细胞质中,但在分化的早期阶段,它们通过将FBS从10%降低到1%而转移到新形成的肌管的核中。在完全分化的肌管中,金属硫蛋白含量随细胞质定位而降低。 MT和Zn亚细胞定位的这些变化伴随着肌管中凋亡的增加。通过DNA梯形成和TUNEL技术测量在分化的不同阶段的细胞凋亡的变化。结果还表明,凋亡可能由自由基产生引发,并可能伴随有p53表达。与L6细胞系相比,H9C2细胞含有高水平的MT,分化缓慢,并且凋亡小体的发生率较低。版权所有1999,学术出版社。

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