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Rejuvenation by cell reprogramming: a new horizon in gerontology

机译:通过细胞重编程复兴:老年医学的新视野

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摘要

The discovery of animal cloning and subsequent development of cell reprogramming technology were quantum leaps as they led to the achievement of rejuvenation by cell reprogramming and the emerging view that aging is a reversible epigenetic process. Here, we will first summarize the experimental achievements over the last 7 years in cell and animal rejuvenation. Then, a comparison will be made between the principles of the cumulative DNA damage theory of aging and the basic facts underlying the epigenetic model of aging, including Horvath’s epigenetic clock. The third part will apply both models to two natural processes, namely, the setting of the aging clock in the mammalian zygote and the changes in the aging clock along successive generations in mammals. The first study demonstrating that skin fibroblasts from healthy centenarians can be rejuvenated by cell reprogramming was published in 2011 and will be discussed in some detail. Other cell rejuvenation studies in old humans and rodents published afterwards will be very briefly mentioned. The only in vivo study reporting that a number of organs of old progeric mice can be rejuvenated by cyclic partial reprogramming will also be described in some detail. The cumulative DNA damage theory of aging postulates that as an animal ages, toxic reactive oxygen species generated as byproducts of the mitochondria during respiration induce a random and progressive damage in genes thus leading cells to a progressive functional decline. The epigenetic model of aging postulates that there are epigenetic marks of aging that increase with age, leading to a progressive derepression of DNA which in turn causes deregulated expression of genes that disrupt cell function. The cumulative DNA damage model of aging fails to explain the resetting of the aging clock at the time of conception as well as the continued vitality of species as millenia go by. In contrast, the epigenetic model of aging straightforwardly explains both biologic phenomena. A plausible initial application of rejuvenation in vivo would be preventing adult individuals from aging thus eliminating a major risk factor for end of life pathologies. Further, it may allow the gradual achievement of whole body rejuvenation.
机译:动物克隆的发现和随后细胞重编程技术的发展是一个巨大的飞跃,因为它们通过细胞重编程导致了复兴,并且出现了衰老是可逆的表观遗传过程的新观点。在这里,我们将首先总结过去7年来在细胞和动物复兴方面的实验成果。然后,将对衰老的累积DNA损伤理论的原理与衰老的表观遗传模型的基本事实(包括Horvath的表观遗传钟)进行比较。第三部分将把这两个模型应用于两个自然过程,即哺乳动物合子中衰老时钟的设定和哺乳动物相继世代的衰老时钟的变化。第一项研究表明健康百岁老人的皮肤成纤维细胞可通过细胞重编程而恢复活力,该研究于2011年发表,并将进行详细讨论。此后将简要提及其他有关老年人和啮齿动物的细胞再生研究。报告中还将详细描述唯一的一项体内研究,该研究报告了许多旧的早衰小鼠器官可以通过循环部分重编程来恢复活力。衰老的累积DNA损伤理论假设,随着动物的衰老,在呼吸过程中作为线粒体副产物生成的有毒活性氧会诱导基因中的随机和进行性损伤,从而导致细胞进行性功能下降。衰老的表观遗传模型假定衰老的表观遗传标志会随着年龄的增长而增加,从而导致DNA的逐步抑制,进而导致破坏细胞功能的基因表达失调。衰老的累积DNA损伤模型无法解释受孕时衰老时钟的重置以及随着千年的过去物种的持续活力。相反,衰老的表观遗传模型直接解释了这两种生物学现象。体内复兴的合理初步应用将防止成年个体的衰老,从而消除生命终结的主要危险因素。此外,它可以逐步实现全身的年轻化。

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