Chen Jian-Hua, Ozanne Susan E, Hales C Nicholas
Department of Clinical Biochemistry, University of Cambridge, Camgbridge, UK.
Methods Mol Biol. 2007;371:179-89. doi: 10.1007/978-1-59745-361-5_14.
Normal human fibroblasts cultured in vitro only have a limited proliferation potential. They eventually become senescent as a result of serial passage, which is commonly known as replicative senescence. This led to the suggestion that cellular senescence might be a cellular basis of human aging. Indeed, cells with the characteristics of senescence accumulate with age in multiple tissues from both humans and rodents, thus implying a role of cellular senescence in aging. Cellular senescence in vitro has, therefore, been regarded as a useful model for elucidating molecular mechanisms that underlie organismal aging. In addition to replicative senescence, cellular senescence can also be induced by various stresses including oxidative stress. Hydrogen peroxide is widely used to achieve oxidative stress-induced premature senescence within a short period of time. Such induced premature senescent cells display many markers that are indistinguishable from replicative senescent cells. Thus, oxidative stress-induced senescent cells serve as an excellent in vitro tool for aging research.
体外培养的正常人成纤维细胞增殖潜力有限。由于连续传代,它们最终会衰老,这就是通常所说的复制性衰老。这引发了一种观点,即细胞衰老可能是人类衰老的细胞基础。事实上,具有衰老特征的细胞在人类和啮齿动物的多个组织中都会随着年龄的增长而积累,这意味着细胞衰老在衰老过程中发挥了作用。因此,体外细胞衰老被视为阐明机体衰老分子机制的有用模型。除了复制性衰老外,细胞衰老还可由包括氧化应激在内的各种应激诱导。过氧化氢被广泛用于在短时间内实现氧化应激诱导的早衰。这种诱导的早衰细胞表现出许多与复制性衰老细胞无法区分的标志物。因此,氧化应激诱导的衰老细胞是衰老研究的优秀体外工具。