Telomere lengths are characteristic in each human individual

被引:232
作者
Takubo, K [1 ]
Izumiyama-Shimomura, N
Honma, N
Sawabe, M
Arai, T
Kato, M
Oshimura, M
Nakamura, KI
机构
[1] Tokyo Metropolitan Inst Gerontol, Dept Clin Pathol, Tokyo 1730015, Japan
[2] Tokyo Metropolitan Geriatr Hosp, Dept Pathol, Tokyo 1730015, Japan
[3] Tottori Univ, Sch Med, Sch Life Sci, Dept Mol & Cell Genet, Yonago, Tottori 6830826, Japan
关键词
telomere length; liver; kidney; brain; heart; spleen; human aging;
D O I
10.1016/S0531-5565(01)00218-2
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
Background. A great deal of attention has been focused on telomeres in relation to cellular aging, immortality, and cancer. However, there is no simple link between telomeres and tissue turnover. We recently proposed a hypothesis that telomere shortening with aging and telomere lengths in different organs are characteristic for human individuals. Methods. To test this, telomere lengths were measured using DNA from cerebral cortex, myocardium, liver, renal cortex and spleen tissues obtained from human subjects ranging in age from neonates to centenarians. Results. Regression analyses demonstrated telomere reduction rates of 29-60 base pair (bp) per year in the liver, renal cortex and spleen, but no such decrease in the cerebral cortex and myocardium. Significant correlation was found between tissues within individuals, such as cerebral cortex versus (vs) myocardium, cerebral cortex vs liver, cerebral cortex vs renal cortex, myocardium vs liver, myocardium vs renal cortex, and liver vs renal cortex. In most cases, the longest telomeres were observed in the myocardium and the shortest in the liver or renal cortex. Conclusions. Telomere lengths did not show clear correlation with tissue renewal times in vivo, but rather were characteristic for individuals. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:523 / 531
页数:9
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