Gonos E S
National Hellenic Research Foundation, Institute of Biological Research and Biotechnology, Laboratory of Molecular and Cellular Ageing, Athens, Greece.
Exp Gerontol. 2000 Feb;35(1):15-21. doi: 10.1016/s0531-5565(99)00075-3.
Aging is a universal phenomenon that affects nearly all animal species. It can be considered as the product of an interaction between genetic, environmental and lifestyle factors, which in turn influence longevity that varies between and within species. Several studies have been focused in healthy centenarians, because these exceptional individuals represent the best example of successful aging. These studies have shown that centenarians have escaped the major age-associated diseases, they have well conserved several immune parameters, and at least one gene allele has been identified and linked with longevity. In parallel, studies at cellular level have identified several genes that influence, positively or negatively, normal replicative in vitro life-span. The ability of these genes to regulate aging in vitro, in conjunction with the telomeres shortening hypothesis have raised the intriguing question of the existence of a molecular clock that counts and thus may modulates human aging and longevity. This review article will discuss these issues, focusing in the nature of the genetic factors that associate with these phenomena.
衰老 是一种影响几乎所有动物物种的普遍现象。它可被视为遗传、环境和生活方式因素之间相互作用的产物,这些因素反过来又会影响物种之间和物种内部各不相同的寿命。有几项研究聚焦于健康的百岁老人,因为这些特殊个体代表了成功衰老的最佳范例。这些研究表明,百岁老人避开了与年龄相关的主要疾病,他们的一些免疫参数保存良好,并且至少已鉴定出一个与长寿相关的基因等位基因。与此同时,细胞水平的研究已经确定了几个对体外正常复制寿命有正向或负向影响的基因。这些基因在体外调节衰老的能力,连同端粒缩短假说,引发了一个有趣的问题,即是否存在一个分子时钟来计数并因此可能调节人类衰老和长寿。这篇综述文章将讨论这些问题,重点关注与这些现象相关的遗传因素的本质。