Cellular senescence and the aging brain

被引:185
|
作者
Chinta, Shankar J. [1 ]
Woods, Georgia [1 ]
Rane, Anand [1 ]
Demaria, Marco [1 ]
Campisi, Judith [1 ,2 ]
Andersen, Julie K. [1 ]
机构
[1] Buck Inst Res Aging, Novato, CA 94945 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA
关键词
Aging; Brain; Cellular senescence; Senescence associated secretory phenotype; Neurodegeneration; MOLECULAR-MECHANISMS; DAMAGE RESPONSE; GROWTH ARREST; IN-VIVO; CELLS; MICROGLIA; CANCER; RAT; AGE; FIBROBLASTS;
D O I
10.1016/j.exger.2014.09.018
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Cellular senescence is a potent anti-cancermechanismthat arrests the proliferation of mitotically competent cells to prevent malignant transformation. Senescent cells accumulate with age in a variety of human and mouse tissues where they express a complex 'senescence-associated secretory phenotype' (SASP). The SASP includes many pro-inflammatory cytokines, chemokines, growth factors and proteases that have the potential to cause or exacerbate age-related pathology, both degenerative and hyperplastic. While cellular senescence in peripheral tissues has recently been linked to a number of age-related pathologies, its involvement in brain aging is just beginning to be explored. Recent data generated by several laboratories suggest that both aging and age-related neurodegenerative diseases are accompanied by an increase in SASP-expressing senescent cells of nonneuronal origin in the brain. Moreover, this increase correlates with neurodegeneration. Senescent cells in the brain could therefore constitute novel therapeutic targets for treating age-related neuropathologies. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:3 / 7
页数:5
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