Telomere attrition of the human abdominal aorta: relationships with age and atherosclerosis

被引:149
作者
Okuda, K
Khan, MY
Skurnick, J
Kimura, M
Aviv, H
Aviv, A
机构
[1] Univ Med & Dent New Jersey, New Jersey Med Sch, Hypertens Res Ctr, Newark, NJ 07103 USA
[2] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Pathol, Newark, NJ 07103 USA
[3] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Prevent Med & Community Hlth, Newark, NJ 07103 USA
[4] Univ Med & Dent New Jersey, New Jersey Med Sch, Ctr Human & Mol Genet, Newark, NJ 07103 USA
关键词
telomeres; aorta; human; age; atherosclerosis;
D O I
10.1016/S0021-9150(99)00482-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Little is known about the turnover rate (i.e. the rate of replication and death) of cells in the intima and media of human arteries as a function of age and atherosclerosis. One indicator of the replicative history of cells is telomere length. In this work we explored the rate of telomere attrition as a function of age and atherosclerosis in cells of the human abdominal aorta. Telomere length, measured by the terminal restriction fragment using Southern analysis, was determined in the intima and media of the distal (infrarenal) versus proximal (suprarenal) segments of the abdominal aorta. Telomere length was then correlated with age and atherosclerotic grade. The rate of age-dependent telomere attrition was higher in both the intima and media of the distal versus proximal abdominal aorta. In addition, telomere length was negatively correlated with atherosclerotic grade. However, after adjustment for age, this relationship was not statistically significant. The high rate of age-dependent telomere attrition in the distal abdominal aorta probably reflects enhanced cellular turnover rate due to local factors such as an increase in shear wall stress in this vascular segment. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:391 / 398
页数:8
相关论文
共 16 条
[1]   TELOMERE LENGTH PREDICTS REPLICATIVE CAPACITY OF HUMAN FIBROBLASTS [J].
ALLSOPP, RC ;
VAZIRI, H ;
PATTERSON, C ;
GOLDSTEIN, S ;
YOUNGLAI, EV ;
FUTCHER, AB ;
GREIDER, CW ;
HARLEY, CB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (21) :10114-10118
[2]   TELOMERES - NO END IN SIGHT [J].
BLACKBURN, EH .
CELL, 1994, 77 (05) :621-623
[3]   TELOMERE LENGTH AND REPLICATIVE AGING IN HUMAN VASCULAR TISSUES [J].
CHANG, E ;
HARLEY, CB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (24) :11190-11194
[4]   SENESCENCE-DEPENDENT REGULATION OF TYPE-1 PLASMINOGEN-ACTIVATOR INHIBITOR IN HUMAN VASCULAR ENDOTHELIAL-CELLS [J].
COMI, P ;
CHIARAMONTE, R ;
MAIER, JAM .
EXPERIMENTAL CELL RESEARCH, 1995, 219 (01) :304-308
[5]   Mechanisms of disease - Antioxidants and atherosclerotic heart disease [J].
Diaz, MN ;
Frei, B ;
Vita, JA ;
Keaney, JF .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (06) :408-416
[6]   Telomeres and senescence: The history, the experiment, the future [J].
Greider, CW .
CURRENT BIOLOGY, 1998, 8 (05) :R178-+
[7]  
GUZMAN MA, 1968, LAB INVEST, V18, P479
[8]   TELOMERES SHORTEN DURING AGING OF HUMAN FIBROBLASTS [J].
HARLEY, CB ;
FUTCHER, AB ;
GREIDER, CW .
NATURE, 1990, 345 (6274) :458-460
[9]   Shortened telomere length in white blood cells of patients with IDDM [J].
Jeanclos, E ;
Krolewski, A ;
Skurnick, J ;
Kimura, M ;
Aviv, H ;
Warram, JH ;
Aviv, A .
DIABETES, 1998, 47 (03) :482-486
[10]  
LUPO F, 1993, ARTERIOSCLER THROMB, V13, P1090