Age dependent aneuploidy and telomere length of the human vascular endothelium

被引:101
作者
Aviv, H
Khan, MY
Skurnick, J
Okuda, K
Kimura, M
Gardner, J
Priolo, L
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, Ctr Human & Mol Genet, Newark, NJ 07103 USA
[3] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Pathol, Newark, NJ 07103 USA
[4] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Prevent Med & Community Hlth, Newark, NJ 07103 USA
关键词
aneuploidy; vascular endothlium; aging; telomeres;
D O I
10.1016/S0021-9150(01)00506-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale: aneuploidy and telomere length are two major parameters that have been associated with cellular senescence in vitro. In order to explore the role of aneuploidy and telomere length in aging of the human vasculature, we studied these two parameters in direct preparations of endothelial cells of the human abdominal aorta. Methods: using fluorescent in situ hybridization on 'touch prep' slides, we evaluated aneuploidy of two autosomes (chromosomes 6 and 16) and sex chromosomes in non cultured endothelial cells of the abdominal aorta as a function of the donor's age. Results: we found that the frequency of aneuploidy of vascular endothelial cells significantly increased with age. This was expressed by age-dependent tetrasomy (r(s) = 0.56, P = 0.006 for chromosome 6; and r(s) = 0.54, P = 0.008 for chromosome 16), and age dependent loss of the Y chromosome (r(s) = 0.85, P = 0.0003). In addition, we found that telomere length was inversely correlated with age (r = -0.38, P = 0.008). Data interpretation: these findings suggest that indicators of cellular senescence, earlier observed in vitro, are also expressed in the human vascular endothelium. in vivo. Aneuploidy and telomere attrition might thus play a role in the aging of the human vasculature. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:281 / 287
页数:7
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