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Methusalem’s mystery

机译:methusalem的奥秘

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摘要

Life is limited—at least for multicellular animals. The separation between differentiating somatic cells and the germ line also delineates the separation between mortality and eternal life. We are so tantalised by induced pluricellular stem cells, because they promise the option to cross this line. However, reprogramming of developmental potential is only part of the story; life leaves traces in a cell that exceed chromatin remodelling. These traces challenge cellular homeostasis, and with time, the cell will yield, a process whose manifestation in multicellular animals is familiar to all of us as ageing. It should be clear that ageing has to be separated from developmental potency; even plants, where induced pluripotency has been developed and biotechnologically exploited already for decades, undergo ageing. Is ageing more than the mere accumulation of life-related damage, or is it rather a predefined programme?A popular theory (Harman 1956) deduces ageing from oxidative damage by radicals, especially reactive oxygen species. This sounds like a fairly general mechanism—is it thus possible to arrive at a universal theory for ageing?
机译:生命是有限的-至少对于多细胞动物而言。分化的体细胞与种系之间的分离也描绘出死亡率与永生之间的分离。诱导的多细胞干细胞使我们如此着迷,因为它们承诺可以越过这条线。然而,对发展潜力的重新编程只是故事的一部分;生命会在细胞中留下超过染色质重塑的痕迹。这些痕迹挑战细胞的体内平衡,随着时间的流逝,细胞将产生产量,这个过程在多细胞动物中的表现随着年龄的增长而为大家所熟悉。应该清楚的是,衰老必须与发展能力分开;甚至已经开发出诱导多能性并且已经进行生物技术开发数十年的植物也会老化。衰老不仅是与生命有关的损害的累积,还是一个预先定义的程序?一种流​​行的理论(Harman,1956年)从自由基尤其是活性氧的氧化损害中推断出衰老。这听起来像是一个相当笼统的机制-从而有可能得出一个关于衰老的普遍理论吗?

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