Senescence in Health and Disease

被引:1265
作者
He, Shenghui [1 ,2 ,3 ]
Sharpless, Norman E. [1 ,2 ,3 ]
机构
[1] Univ N Carolina, Sch Med, Dept Med, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Sch Med, Dept Genet, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Sch Med, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
关键词
DNA-DAMAGE RESPONSE; HEMATOPOIETIC STEM-CELLS; PANCREATIC BETA-CELLS; CELLULAR SENESCENCE; SECRETORY PHENOTYPE; TUMOR SUPPRESSION; IN-VIVO; ANTIVIRAL DEFENSE; CANCER RESISTANCE; FAMILY-MEMBERS;
D O I
10.1016/j.cell.2017.05.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many cellular stresses activate senescence, a persistent hyporeplicative state characterized in part by expression of the p16(INK4a) cell-cycle inhibitor. Senescent cell production occurs throughout life and plays beneficial roles in a variety of physiological and pathological processes including embryogenesis, wound healing, host immunity, and tumor suppression. Meanwhile, the steady accumulation of senescent cells with age also has adverse consequences. These non-proliferating cells occupy key cellular niches and elaborate pro-inflammatory cytokines, contributing to aging-related diseases and morbidity. This model suggests that the abundance of senescent cells in vivo predicts "molecular," as opposed to chronologic, age and that senescent cell clearance may mitigate aging-associated pathology.
引用
收藏
页码:1000 / 1011
页数:12
相关论文
共 99 条
  • [11] Aging, Cellular Senescence, and Cancer
    Campisi, Judith
    [J]. ANNUAL REVIEW OF PHYSIOLOGY, VOL 75, 2013, 75 : 685 - 705
  • [12] Clearance of senescent cells by ABT263 rejuvenates aged hematopoietic stem cells in mice
    Chang, Jianhui
    Wang, Yingying
    Shao, Lijian
    Laberge, Remi-Martin
    Demaria, Marco
    Campisi, Judith
    Janakiraman, Krishnamurthy
    Sharpless, Norman E.
    Ding, Sheng
    Feng, Wei
    Luo, Yi
    Wang, Xiaoyan
    Aykin-Burns, Nukhet
    Krager, Kimberly
    Ponnappan, Usha
    Hauer-Jensen, Martin
    Meng, Aimin
    Zhou, Daohong
    [J]. NATURE MEDICINE, 2016, 22 (01) : 78 - +
  • [13] PDGF signalling controls age-dependent proliferation in pancreatic β-cells
    Chen, Hainan
    Gu, Xueying
    Liu, Yinghua
    Wang, Jing
    Wirt, Stacey E.
    Bottino, Rita
    Schorle, Hubert
    Sage, Julien
    Kim, Seung K.
    [J]. NATURE, 2011, 478 (7369) : 349 - +
  • [14] Senescence-like changes induced by expression of p21Waf1/Cip1 in NIH3T3 cell line
    Chen, X
    Zhang, W
    Gao, YF
    Su, XQ
    Zhai, ZH
    [J]. CELL RESEARCH, 2002, 12 (3-4) : 229 - 233
  • [15] Control of the senescence-associated secretory phenotype by NF-κB promotes senescence and enhances chemosensitivity
    Chien, Yuchen
    Scuoppo, Claudio
    Wang, Xiaowo
    Fang, Xueping
    Balgley, Brian
    Bolden, Jessica E.
    Premsrirut, Prem
    Luo, Weijun
    Chicas, Agustin
    Lee, Cheng S.
    Kogan, Scott C.
    Lowe, Scott W.
    [J]. GENES & DEVELOPMENT, 2011, 25 (20) : 2125 - 2136
  • [16] Senescent intimal foam cells are deleterious at all stages of atherosclerosis
    Childs, Bennett G.
    Baker, Darren J.
    Wijshake, Tobias
    Conover, Cheryl A.
    Campisi, Judith
    van Deursen, Jan M.
    [J]. SCIENCE, 2016, 354 (6311) : 472 - 477
  • [17] Cellular senescence in aging and age-related disease: from mechanisms to therapy
    Childs, Bennett G.
    Durik, Matej
    Baker, Darren J.
    van Deursen, Jan M.
    [J]. NATURE MEDICINE, 2015, 21 (12) : 1424 - 1435
  • [18] Senescence and apoptosis: dueling or complementary cell fates?
    Childs, Bennett G.
    Baker, Darren J.
    Kirkland, James L.
    Campisi, Judith
    van Deursen, Jan M.
    [J]. EMBO REPORTS, 2014, 15 (11) : 1139 - 1153
  • [19] Chou JP, 2013, CURR PHARM DESIGN, V19, P1680
  • [20] Cell fusion induced by ERVWE1 or measles virus causes cellular senescence
    Chuprin, Anna
    Gal, Hilah
    Biron-Shental, Tal
    Biran, Anat
    Amiel, Aliza
    Rozenblatt, Shmuel
    Krizhanovsky, Valery
    [J]. GENES & DEVELOPMENT, 2013, 27 (21) : 2356 - 2366