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衰老相关分泌表型的研究进展 被引量:11

The research progress of senescence-associated secretory phenotype
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摘要 细胞衰老的同时常伴随着衰老相关分泌表型(senescence-associated secretory phenotype,SASP)的产生。SASP由促炎细胞因子、生长因子、趋化因子和基质重塑酶等一系列细胞因子组成,它们可以导致机体慢性低度炎症和疾病,并可以反作用于衰老细胞及其邻近细胞加速它们的衰老进程,并可作为新的细胞衰老效应机制。该文通过对SASP生物学功效、分泌调节、机制、以及与相关疾病关联的探讨,提高我们对SASP的认知,引发我们对SASP相关疾病疗法的思考。 When senescence induction is based on DNA damage,senescent cells display a unique phenotype,which has been termed 'senescence-associated secretory phenotype '( SASP).SASP, including proinflammatory cytokines, growth factors,chemokines,matrix remodeling enzymes and other cytokines,may be an important driver of chronic inflammation and therefore may be part of a vicious cycle of inflammation,DNA damage and senescence. Senescence-associated secretory products released by such cells can affect the neighboring cells and further exacerbate their regenerative capacity. SASP is associated with many chronic age-related diseases.
出处 《中国药理学通报》 CAS CSCD 北大核心 2016年第11期1505-1509,共5页 Chinese Pharmacological Bulletin
基金 国家自然科学基金资助项目(No 81274130) 上海市教委085项目高等教育内涵建设基金项目(No 085ZY1202)
关键词 细胞衰老 衰老相关分泌表型 SASP 炎症 衰老机制 衰老相关疾病 cellular senescence senescence-associated secretory phenotype SASP inflammation aging mechanism age-related diseases
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  • 1Wang Y,Schulte B A,LaRue A C,et al.Total body irradiation selectively induces murine hematopoietic stem cell senescence[J].Blood,2006,107(1):358-66.
  • 2Meng A,Wang Y,Brown S A,et al.Ionizing radiation and busulfan inhibit murine bone marrow cell hematopoietic function via apoptosis-dependent and-independent mechanisms[J].Exp Hematol,2003,31(12):1348-56.
  • 3Luo J,Nikolaev A Y,Imai S,et al.Negative control of p53 by Sir2alpha promotes cell survival under stress[J].Cell,2001,107(2):137-48.
  • 4Kaeberlein M,McVey M,Guarente L.The SIR2/3/4 complex and SIR2 alone promote longevity in Saccharomyces cerevisiae by two different mechanisms[J].Genes Dev,1999,13(19):2570-80.
  • 5Boily G,Seifert E L,Bevilacqua L,et al.SirT1 regulates energy metabolism and response to caloric restriction in mice[J].PLoS One,2008,3(3):e1759.
  • 6Brunet A,Sweeney L B,Sturgill J F,et al.Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase[J].Science,2004,303(5666):2011-5.
  • 7Berthiaume M,Boufaied N,Moisan A,et al.High levels of oxidative stress globally inhibit gene transcription and histone acetylation[J].DNA Cell Biol,2006,25(2):124-34.
  • 8Tothova Z,Kollipara R,Huntly B J,et al.FoxOs are critical mediators of hematopoietic stem cell resistance to physiologic oxidative stress[J].Cell,2007,128(2):325-39.
  • 9Han M K,Song E K,Guo Y,et al.SIRT1 regulates apoptosis and Nanog expression in mouse embryonic stem cells by controlling p53 subcellular localization[J].Cell Stem Cell,2008,2(3):241-51.
  • 10Michelle M. Richardson,Julie R. Jonsson,Elizabeth E. Powell,Elizabeth M. Brunt,Brent A. Neuschwander–Tetri,Prithi S. Bhathal,John B. Dixon,Martin D. Weltman,Herbert Tilg,Alexander R. Moschen,David M. Purdie,Anthony J. Demetris,Andrew D. Clouston.Progressive Fibrosis in Nonalcoholic Steatohepatitis: Association With Altered Regeneration and a Ductular Reaction[J].Gastroenterology.2007(1)

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