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BJ fibroblasts display high antioxidant capacity and slow telomere shortening independent of hTERT transfection

Lookup NU author(s): Dr Gabriele Saretzki, Professor Thomas von Zglinicki

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Abstract

Human foreskin BJ fibroblasts are well protected against oxidative stress as shown by their low intracellular peroxide content, low levels of protein carbonyls, and low steady-state lipofuscin content as compared to other primary human fibroblasts. This correlates with a long replicative life span of the parental cells of about 90 population doublings and a telomere-shortening rate of only 15-20 bp/PD. This value might define the upper limit of a telomere-shortening rate that can still be explained by the end replication problem alone. In BJ clones immortalized by transfection with hTERT, the catalytic subunit of telomerase, the same telomere-shortening rate as in parental cells is observed over a long time despite strong telomerase activity. Hyperoxia, which induces oxidative stress and accelerates telomere shortening in a variety of human fibroblast strains, does not do so in BJ cells. It is possible that the high antioxidative capacity of BJ cells, by minimizing the accumulation of genomic damage, is instrumental in the successful immortalization of these cells by telomerase. © 2001 Elsevier Science Inc.


Publication metadata

Author(s): Saretzki G; Von Zglinicki T; Lorenz M; Sitte N; Metzkow S

Publication type: Article

Publication status: Published

Journal: Free Radical Biology and Medicine

Year: 2001

Volume: 31

Issue: 6

Pages: 824-831

ISSN (print): 0891-5849

ISSN (electronic): 1873-4596

Publisher: Elsevier

URL: http://dx.doi.org/10.1016/S0891-5849(01)00664-5

DOI: 10.1016/S0891-5849(01)00664-5

PubMed id: 11557321


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