首页> 外文期刊>Experimental Gerontology >Two-dimensional gel electrophoretic studies on the cellular aging: accumulation of alpha-2-macroglobulin in human fibroblasts with aging.
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Two-dimensional gel electrophoretic studies on the cellular aging: accumulation of alpha-2-macroglobulin in human fibroblasts with aging.

机译:细胞衰老的二维凝胶电泳研究:随着年龄的增长,人成纤维细胞中α-2-巨球蛋白的积累。

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To understand the mechanisms that control life span and age-related phenotypes, we used two-dimensional (2D) gel electrophoresis to study the intracellular proteins whose amounts change during the process of cellular aging. We found that the amount of an alpha-2-macroglobulin (A2M) fragment derived from culture medium increased in the cells with aging. A2M is linked to Alzheimer's disease both genetically and functionally. This is the first report of accumulation of an A2M fragment in senescent fibroblasts. We also studied 2D gel profiles of human fibroblasts immortalized by treatment with either 60Co gamma rays or 4-nitroquinoline 1-oxide. As immortalized cells overcome cellular senescence to gain an unlimited life span, the proteins whose amounts change after immortalization may be relevant to the age-related phenotypes. 2D gel analysis revealed that the A2M fragment was down-regulated in the immortalized cells, compared with their normal counterparts, regardless of their passage. We also found that the other four proteins increased in amount with aging and decreased in amount after immortalization. Our results suggest: (1) the A2M incorporation into the cells is increased in the process of cellular aging; and (2) A2M may be linked to the age-related phenotypes that were lost during the process of immortalization of human cells.
机译:为了了解控制寿命和年龄相关表型的机制,我们使用了二维(2D)凝胶电泳技术来研究细胞内蛋白质的数量,这些蛋白质在细胞衰老过程中会发生变化。我们发现,随着年龄的增长,源自培养基的α-2-巨球蛋白(A2M)片段的数量会增加。 A2M在遗传和功能上均与阿尔茨海默氏病相关。这是A2M片段在衰老的成纤维细胞中积累的第一个报道。我们还研究了通过60Coγ射线或4-硝基喹啉1-氧化物处理永生化的人成纤维细胞的2D凝胶分布。随着永生化细胞克服细胞衰老而获得无限的寿命,永生化后数量发生变化的蛋白质可能与年龄相关的表型有关。 2D凝胶分析表明,与永生化细胞相比,永生化细胞中的A2M片段均被下调,无论其传代如何。我们还发现,其他四种蛋白质的数量随着年龄的增长而增加,而永生化后的数量则减少。我们的研究结果表明:(1)细胞衰老过程中A2M掺入细胞的数量增加; (2)A2M可能与在人类细胞永生化过程中丧失的与年龄有关的表型有关。

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