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雷帕霉素诱导细胞自噬在衰老相关疾病中的作用 被引量:17

Effects of rapamycin induced cellular autophagy in aging-related diseases
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摘要 哺乳动物雷帕霉素靶蛋白(mammalian target of rapamycin,m TOR)是衰老和衰老相关疾病的一个关键调节因子。雷帕霉素(rapamycin,RAPA)可通过抑制m TOR通路,诱导和促进细胞自噬的发生。细胞自噬是维持细胞内稳态的主要方式与途径,通过降解多余的、受损的及衰老的蛋白与细胞器,为细胞重建、再生和修复提供必需原料。早老症(hutchinson-gilford progeria syndrome,HGPS)患者细胞中伴随早老蛋白(progerin)的异常聚集;此外,诸如亨廷顿病、帕金森病、阿尔茨海默病等神经退行性疾病细胞内同样出现异常蛋白质的聚集,而这些异常蛋白的清除正依赖于细胞的自噬作用。由此可见,雷帕霉素是潜在的抗衰老、治疗早老症及衰老相关疾病的重要药物。该文主要阐述雷帕霉素促进细胞自噬方面的功能及在HGPS、神经退行性疾病方面的应用。 Mammalian target of rapamycin( mTOR) is a key reg-ulator of aging and aging-related diseases. Rapamycin ( RAPA) induces and promotes the process of cell autophagy through in-hibiting mTOR pathway. Autophagy exerts a crucial role in main-taining the cellular meostasis, which provides essential materials for cell reconstruction, regeneration and repair via degradating the redundant, damaged, or senescent proteins and organelles. Hutchinson Gilford progeria syndrome ( HGPS ) patients are al-ways accompanied with abnormally accumulated progerin in cells. Similar to HGPS, abnormal protein accumulation is the common pathological feature of neurodegenerative diseases, in-cluding Huntington′s disease, Parkinson′s disease, Alzheimer′s disease and so on. Degradation of these abnormal proteins pre-dominantly depends on cell autophagy. Thus, rapamycin is a po-tential anti-aging drug for HGPS and aging-related diseases thera-py. This view focuses on the effects of rapamycin on cell autoph-agy and clinical application in HGPS and neurodegenerative dis-eases.
出处 《中国药理学通报》 CAS CSCD 北大核心 2015年第1期11-14,共4页 Chinese Pharmacological Bulletin
基金 国家自然科学基金资助项目(No 30900739 81170327 31201036) 广东省自然科学基金资助项目(No 9152402301000007) 东莞市科技计划(No 2008108101062 2012108102022)
关键词 雷帕霉素 雷帕霉素靶蛋白 自噬 早老症 早老蛋白 神经退行性疾病 rapamycin TOR autophagy HGPS progerin neurodegenerative diseases
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参考文献30

  • 1Laplante M,Sabatini D M.Mtor signaling at a glance[J].J Cell Sci,2009,122(Pt 20):3589-94.
  • 2Bjedov I,Partridge L.A longer and healthier life with tor downregulation:Genetics and drugs[J].Biochem Soc Trans,2011,39(2):460-5.
  • 3Powers R W 3rd,Kaeberlein M,Caldwell S D,et al.Extension of chronological life span in yeast by decreased tor pathway signaling[J].Genes Dev,2006,20(2):174-84.
  • 4Fabrizio P,Pozza F,Pletcher S D,et al.Regulation of longevity and stress resistance by sch9 in yeast[J].Science,2001,292(5515):288-90.
  • 5Robida-Stubbs S,Glover-Cutter K,Lamming D W,et al.Tor signaling and rapamycin influence longevity by regulating skn-1/nrf and daf-16/foxo[J].Cell Met,2012,15(5):713-24.
  • 6Bjedov I,Toivonen J M,Kerr F,et al.Mechanisms of life span extension by rapamycin in the fruit fly drosophila melanogaster[J].Cell Met,2010,11(1):35-46.
  • 7Harrison D E,Strong R,Sharp Z D,et al.Rapamycin fed late in life extends lifespan in genetically heterogeneous mice[J].Nature,2009,460(7253):392-5.
  • 8Fok W C,Chen Y,Bokov A,et al.Mice fed rapamycin have an increase in lifespan associated with major changes in the liver transcriptome[J].PLo S One,2014,9(1):e83988.
  • 9Medvedik O,Lamming D W,Kim K D,et al.Msn2 and msn4link calorie restriction and tor to sirtuin-mediated lifespan extension in saccharomyces cerevisiae[J].PLo S Biol,2007,5(10):e261.
  • 10Johnson S C,Rabinovitch P S,Kaeberlein M.Mtor is a key modulator of ageing and age-related disease[J].Nature,2013,493(7432):338-45.

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