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与细胞衰老相关的sirtuin家族 被引量:3

Research progress of sirtuins involved in cellular senescence
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摘要 衰老是发育过程中的普遍现象,是生理功能衰退过程中呈现的一系列特定变化,趋向于疾病发生的复杂过程。细胞衰老是由于端粒缩短、DNA损伤、氧化应激和原癌基因激活中特征分子的改变等产生的一种生理变化。本篇综述通过总结衰老信号通路中的年龄相关基因sirtuins家族与核因子(NF)-κB转录因子家族、p53、FoxO、PGC-1、mTOR等的相互作用,为我们研究衰老进程并在延缓衰老和自然死亡方面提供了可靠的依据。 Aging,one of the pervasive developmental processes,is a complex ensemble of physiological functional decay and a risk factor for many diseases.The mechanism of cellular senescence involves telomere attrition,DNA damage,and characteristic molecular changes in oxidative stress,oncogene activation and so on.In this review,we summarized some significant ageassociated genes in senescence signaling pathway including Sirt family,NF-κB transcription factors,p53,FoxO,PGC-1and mTOR,which are useful to understand the aging process and ultimately postpone ageing and natural death.
出处 《生命的化学》 CAS CSCD 北大核心 2010年第5期744-750,共7页 Chemistry of Life
基金 国家重点基础研究发展计划(2009CB941001)资助
关键词 细胞衰老 sirtuins家族 P53 NF-κB FOXO PGC-1 MTOR senescence Sirt p53 NF-κB FoxO PGC-1 mTOR
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参考文献53

  • 1Saunders LR et al. Sirtuins: critical regulators at the crossroads between cancer and aging. Oncogene, 2007, 26:5489-5504.
  • 2Bordone L et al. Calorie restriction, Sirtl and metabolism: understanding longevity. Nat Rev Mol Cell Biol, 2005, 6: 298- 305.
  • 3Cohen HY et al. Calorie restriction promotes mammalian cell survival by inducing the Sirtl deacetylase. Science, 2004, 305:390-392.
  • 4Chen D et al. Increase in activity during calorie restriction requires Sirtl. Science, 2005, 310:1641.
  • 5Lin SJ et al. Calorie restriction extends Saccharomyces cerevisiae lifespan by increasing respiration. Nature, 2002, 418:344-348.
  • 6Howitz KT et al. Small molecule activators of Sirtuins extend Saccharo mycescerevisiae lifespan. Nature, 2003, 425: 191- 196.
  • 7Nisoli E et al. Calorie restriction promotes mitochondrial biogenesis by inducing the expression of eNOS. Science, 2005, 310:314-317.
  • 8Schmelzle T et al. TOR, a central controller of cell growth. Cell, 2000, 103:253-262.
  • 9Singhee H et al. Ghosh Sirtl negatively regulates the mammalian target of rapamycin. PLoS ONE, 2010, 5:e9199.
  • 10Adler AS et al. Motif module map reveals enforcement of aging by continual NF-rd3 activity. Genes Dev, 2007, 21:3244-3257.

同被引文献14

  • 1郭亦琦,施冬云,王君晖,刘珊林.Sirt基因家族及其对细胞寿命的调节[J].生物物理学报,2006,22(1):7-11. 被引量:9
  • 2CHENG Q, ZHANG Z, ZHANG S, et al. Human umbilical cord mesenchymal stem ceils protect against ischemic brain injury in mouse by regulating peripheral immunoinflamma- tion[ J]. Brain Res ,2015,1594:293.
  • 3CHENG T, YANG B, LI D, et al. Wharton's jelly transplan- tation improves neurologie function in a rat model of trau- matic brain injury[ J ]. Cell Mol Neurobiol, 2015,35 ( 5 ) : 641.
  • 4HARTING K, KNOLL B. SIRT2-mediated protein deacety-lation:an emerging key regulator in brain physiology and pathology[J]. Eur J Cell Biol,2010,89(2/3 ) :262.
  • 5DE OLIVEIRA RM,SARKANDER J, KAZANTSEV AG, et al. SIRT2 as a therapeutic target for age-related disorders [ J]. Front Pharmacol,2012 ,3 :82.
  • 6BRAIDY N, POLJAK A, GRANT R, et al. Differential ex- pression of sirtuins in the aging rat brain [ J ]. Front Cell Neurosci,2015,9 : 167.
  • 7NORTH B J, ROSENBERG MA, JEGANATHAN KB, et al. SIRT2 induces the checkpoint kinase BubR1 to increase li- fespan[J]. EMBO J,2014,33(13) :1438.
  • 8单志新,林秋雄,李晓红,邓春玉,周志凌,黄薇,黄晓忠,余细勇.腺病毒表达载体对骨髓间充质干细胞分化能力的影响[J].南方医科大学学报,2008,28(7):1132-1135. 被引量:8
  • 9李军,魏继武,蒋爱芹.SIRT6——一个重要的寿命和肿瘤调控蛋白质[J].生命的化学,2013,33(5):514-520. 被引量:4
  • 10谢振华,吴耀炯.主要干性基因与衰老相关基因表达水平的相互拮抗关系[J].生物化学与生物物理进展,2014,41(7):627-631. 被引量:5

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