Telomere uncapping and vascular aging

被引:31
|
作者
Morgan, R. Garrett [1 ]
Donato, Anthony J. [1 ,2 ,3 ]
Walker, Ashley E. [1 ,4 ]
机构
[1] Univ Utah, Dept Internal Med, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Nutr & Integrat Physiol, Salt Lake City, UT USA
[3] Vet Affairs Med Ctr, Geriatr Res Educ & Clin Ctr, Salt Lake City, UT 84148 USA
[4] Univ Oregon, Dept Human Physiol, 122 Esslinger Hall,1240 Univ Oregon, Eugene, OR 97403 USA
关键词
aging; senescence; telomere dysfunction; vascular function; ENDOTHELIAL-CELL; IN-VITRO; SECRETORY PHENOTYPE; SENESCENCE; AGE; LENGTH; ARTERIAL; ATHEROSCLEROSIS; INFLAMMATION; DYSFUNCTION;
D O I
10.1152/ajpheart.00008.2018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although most telomere biology research continues to focus on telomere shortening, there is increasing evidence that telomere deprotection, or "uncapping," is more biologically and possibly clinically important. Telomeres form t-loops to prevent the chromosome ends from appearing as a double-stranded DNA break and initiating a DNA damage response. Breakdown of the t-loop structure, referred to as uncapping, can lead to cellular senescence, increased oxidative stress, and inflammation in tissues. In this review, we describe how telomere uncapping potentially leads to age-related vascular dysfunction and increased cellular senescence, oxidative stress, and inflammation. Importantly, we present evidence to argue that telomere uncapping is more biologically relevant than telomere shortening and a better marker of vascular aging and target for antiaging interventions.
引用
收藏
页码:H1 / H5
页数:5
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