Induction of telomere shortening and replicative senescence by cryopreservation

被引:39
作者
Honda, S
Weigel, A
Hjelmeland, LM
Handa, JT
机构
[1] Univ Calif Davis, Dept Ophthalmol, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Mol & Cellular Biol, Davis, CA 95616 USA
基金
美国国家卫生研究院;
关键词
retinal pigment epithelium; cryopreservation; senescence; telomere; reactive oxygen species;
D O I
10.1006/bbrc.2001.4585
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
Cryopreservation can alter cellular function under certain conditions. In this report, we demonstrate the induction of cellular senescence after cells have been cryopreserved using a standard protocol. A retinal pigment epithelial cell line frozen at a specific freezing rate and subsequently thawed showed severely impaired proliferation compared to cells that were not cryopreserved. The induction of senescence was suggested by senescent associated beta -galactosidase activity and diminished bromo-deoxyuridine incorporation. A remarkable increase of single-strand DNA breaks in terminal restriction fragment (TRF) were found in cryopreserved cells immediately after thawing. The rate of mean TRF length shortening was accelerated after cryopreservation. Given this evidence, we hypothesize that cryopreservation may cause telomere shortening and cellular senescence under certain freezing conditions. (C) 2001 Academic Press.
引用
收藏
页码:493 / 498
页数:6
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