Kleemeier Award Lecture 2008-025EFThe Canary in the Coal Mine: Telomeres and Human Healthspan

被引:42
作者
Effros, Rita B. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, UCLA AIDS Inst, Los Angeles, CA 90095 USA
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2009年 / 64卷 / 05期
基金
美国国家卫生研究院;
关键词
Kleemeier award lecture; Telomeres; Human healthspan; Immune; T cells; T-CELLS; REPLICATIVE SENESCENCE; INFLAMMATORY CYTOKINES; SHORTENED TELOMERES; ASSOCIATION; EXPANSIONS; PHENOTYPE; SUBSETS; DECLINE; LENGTH;
D O I
10.1093/gerona/glp001
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
Telomeres, the repeated series of DNA sequences that cap the ends of linear chromosomes, become shorter during cell division and oxidative stress. Shortened telomeres have been documented in a wide variety of pathologies associated with aging and are also predictive of early mortality in the very old. However, telomere shortening-025EFlike the canary in the coal mine-025EFis not the cause of the deleterious effects, but rather, the harbinger of increased health risk. Using immune responses to infection as a model system to further analyze the link between telomeres and age-related disease, we have demonstrated that the end-stage T cell with shortened telomeres is reduced in antiviral immune function and secretes large amounts of so-called proinflammatory factors. Our research has documented that maintaining high levels of the telomere-extending enzyme, telomerase, by either genetic manipulation or exposure of T cells to chemical telomerase activators, not only retards telomere loss but also restores a more youthful functional profile to the T cells. These observations suggest possible novel telomerase-based therapeutic approaches to enhancing healthspan in the elderly population.
引用
收藏
页码:511 / 515
页数:5
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