Telomerase activation induces elongation of the telomeric single-stranded overhang, but does not prevent chromosome aberrations in human vascular endothelial cells

被引:31
作者
Anno, Kumiko
Hayashi, Akane
Takahashi, Tomoko
Masui, Youp
Ide, Toshinori
Tahara, Hidetoshi [1 ]
机构
[1] Hiroshima Univ, Grad Sch Biomed Sci, Div Integrated Med Sci, Dept Cellular & Mol Biol, Hiroshima 7348553, Japan
[2] Tokushima Bunri Univ, Fac Pharmaceut Sci, Dept Pharmaceut Technol, Physiol Chem Lab, Kagawa 7692193, Japan
[3] Hiroshima Int Univ, Fac Pharmaceut Sci, Cellular & Mol Biol Lab, Hiroshima 7370112, Japan
关键词
telomere; telomerase; TERT; 3' telomeric overhang; G-tail; endothelial cells; immortalization; chromosome; telomere binding protein;
D O I
10.1016/j.bbrc.2006.12.112
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chromosome aberrations such as loss of chromosome 13 were frequently observed in human endothelial cells from umbilical cord veins (HUVEC). A recent study showed that the length of telomeric single-stranded 3'-overhangs (G-tails) is more important as an essential structure for chromosome maintenance than the net telomere length in telomere t-loop formation. Here, we have examined G-tail length using G-tail telomere HPA in normal and hTERT-transduced HUVECs. We found that forced expression of hTERT in HUVEC induced G-tail as well as total telomere length elongation. G-tail length was well correlated with total telomere length. However, hTERT introduction did not prevent chromosome aberrations such as loss of chromosome 13. Normal characteristics such as morphology, up-regulation of vWF, and tube formation were observed in hTERT-HUVEC as in young normal HUVEC. These results show that chromosome aberrations in HUVEC are independent of telomere G-tail and total telomere attrition. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:926 / 932
页数:7
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