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衰老灵长类动物中的细胞衰老

Cellular senescence in aging primates.

作者信息

Herbig Utz, Ferreira Mark, Condel Laura, Carey Dee, Sedivy John M

机构信息

Department of Molecular Biology, Cell Biology, and Biochemistry, Brown University, Providence, RI 02903, USA.

出版信息

Science. 2006 Mar 3;311(5765):1257. doi: 10.1126/science.1122446. Epub 2006 Feb 2.

DOI:10.1126/science.1122446
PMID:16456035
Abstract

The aging of organisms is characterized by a gradual functional decline of all organ systems. Mammalian somatic cells in culture display a limited proliferative life span, at the end of which they undergo an irreversible cell cycle arrest known as replicative senescence. Whether cellular senescence contributes to organismal aging has been controversial. We investigated telomere dysfunction, a recently discovered biomarker of cellular senescence, and found that the number of senescent fibroblasts increases exponentially in the skin of aging baboons, reaching >15% of all cells in very old individuals. In addition, the same cells contain activated ataxia-telangiectasia mutated kinase and heterochromatinized nuclei, confirming their senescent status.

摘要

生物体的衰老特征是所有器官系统功能逐渐衰退。培养中的哺乳动物体细胞具有有限的增殖寿命,在此寿命结束时,它们会经历一种不可逆的细胞周期停滞,即复制性衰老。细胞衰老是否导致生物体衰老一直存在争议。我们研究了端粒功能障碍,这是一种最近发现的细胞衰老生物标志物,发现衰老狒狒皮肤中衰老成纤维细胞的数量呈指数增长,在非常年老的个体中达到所有细胞的15%以上。此外,这些相同的细胞含有活化的共济失调毛细血管扩张突变激酶和异染色质化的细胞核,证实了它们的衰老状态。

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1
Cellular senescence in aging primates.衰老灵长类动物中的细胞衰老
Science. 2006 Mar 3;311(5765):1257. doi: 10.1126/science.1122446. Epub 2006 Feb 2.
2
Critical telomere shortening regulated by the ataxia-telangiectasia gene acts as a DNA damage signal leading to activation of p53 protein and limited life-span of human diploid fibroblasts. A review.由共济失调毛细血管扩张症基因调控的关键端粒缩短作为一种DNA损伤信号,导致p53蛋白激活并限制人类二倍体成纤维细胞的寿命。综述。
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Irreversible cellular senescence induced by prolonged exposure to H2O2 involves DNA-damage-and-repair genes and telomere shortening.长期暴露于过氧化氢诱导的不可逆细胞衰老涉及DNA损伤与修复基因以及端粒缩短。
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Downregulation of transcription factor, Sp1, during cellular senescence.细胞衰老过程中转录因子Sp1的下调。
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ATM-dependent telomere loss in aging human diploid fibroblasts and DNA damage lead to the post-translational activation of p53 protein involving poly(ADP-ribose) polymerase.衰老的人类二倍体成纤维细胞中依赖 ATM 的端粒丢失和 DNA 损伤导致 p53 蛋白的翻译后激活,这一过程涉及聚(ADP - 核糖)聚合酶。
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Telomere dysfunction and stem cell ageing.端粒功能障碍与干细胞衰老。
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Proinflammatory cytokine-induced cellular senescence of biliary epithelial cells is mediated via oxidative stress and activation of ATM pathway: a culture study.促炎细胞因子诱导的胆管上皮细胞衰老通过氧化应激和ATM途径激活介导:一项培养研究
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Cancer, aging and cellular senescence.癌症、衰老与细胞衰老
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Human cell senescence as a DNA damage response.人类细胞衰老作为一种DNA损伤反应。
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