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本文引用的文献

1
Delayed kinetics of DNA double-strand break processing in normal and pathological aging.正常衰老和病理性衰老过程中DNA双链断裂修复的延迟动力学
Aging Cell. 2008 Jan;7(1):89-100. doi: 10.1111/j.1474-9726.2007.00354.x. Epub 2007 Dec 19.
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Role of telomeres in vascular senescence.端粒在血管衰老中的作用。
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Studying telomeres in a longitudinal population based study.在一项基于纵向人群的研究中对端粒进行研究。
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Aging, graying and loss of melanocyte stem cells.黑素细胞干细胞的衰老、白化及丧失。
Stem Cell Rev. 2007 Fall;3(3):212-7. doi: 10.1007/s12015-007-0028-0.
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Leukocytes of exceptionally old persons display ultra-short telomeres.高龄老人的白细胞表现出超短的端粒。
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Telomere length, stem cells and aging.端粒长度、干细胞与衰老。
Nat Chem Biol. 2007 Oct;3(10):640-9. doi: 10.1038/nchembio.2007.38.
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Accelerated telomere shortening and replicative senescence in human fibroblasts overexpressing mutant and wild-type lamin A.在过表达突变型和野生型核纤层蛋白A的人成纤维细胞中,端粒加速缩短和复制性衰老。
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Premature senescence of mesothelial cells is associated with non-telomeric DNA damage.间皮细胞的过早衰老与非端粒DNA损伤有关。
Biochem Biophys Res Commun. 2007 Oct 26;362(3):707-11. doi: 10.1016/j.bbrc.2007.08.047. Epub 2007 Aug 20.
9
Cellular senescence: when bad things happen to good cells.细胞衰老:当好事发生在好细胞上时。 (注:原英文表述似乎不太符合正常逻辑,正常应该是不好的事情发生在细胞上才会导致衰老,这里按照字面意思翻译)
Nat Rev Mol Cell Biol. 2007 Sep;8(9):729-40. doi: 10.1038/nrm2233.
10
Cellular senescence in cancer and aging.癌症与衰老中的细胞衰老
Cell. 2007 Jul 27;130(2):223-33. doi: 10.1016/j.cell.2007.07.003.

细胞衰老与机体衰老。

Cellular senescence and organismal aging.

作者信息

Jeyapalan Jessie C, Sedivy John M

机构信息

Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, RI 02912, USA.

出版信息

Mech Ageing Dev. 2008 Jul-Aug;129(7-8):467-74. doi: 10.1016/j.mad.2008.04.001. Epub 2008 Apr 12.

DOI:10.1016/j.mad.2008.04.001
PMID:18502472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3297662/
Abstract

Cellular senescence, first observed and defined using in vitro cell culture studies, is an irreversible cell cycle arrest which can be triggered by a variety of factors. Emerging evidence suggests that cellular senescence acts as an in vivo tumor suppression mechanism by limiting aberrant proliferation. It has also been postulated that cellular senescence can occur independently of cancer and contribute to the physiological processes of normal organismal aging. Recent data have demonstrated the in vivo accumulation of senescent cells with advancing age. Some characteristics of senescent cells, such as the ability to modify their extracellular environment, could play a role in aging and age-related pathology. In this review, we examine current evidence that links cellular senescence and organismal aging.

摘要

细胞衰老最早是通过体外细胞培养研究观察和定义的,是一种不可逆的细胞周期停滞,可由多种因素触发。新出现的证据表明,细胞衰老通过限制异常增殖而作为一种体内肿瘤抑制机制。也有人推测,细胞衰老可以独立于癌症发生,并有助于正常机体衰老的生理过程。最近的数据表明,衰老细胞会随着年龄的增长在体内积累。衰老细胞的一些特征,如改变其细胞外环境的能力,可能在衰老和与年龄相关的病理过程中起作用。在这篇综述中,我们研究了将细胞衰老与机体衰老联系起来的当前证据。