Abstract
Replicative senescence of T cells is correlated with erosion of telomere ends. Telomerase plays a key role in maintaining telomere length. Therefore, it is thought that telomerase regulates the life span of T cells. To test this hypothesis, we have over-expressed human telomerase reverse transcriptase in human CD8+ T cells. Ectopic expression of human telomerase reverse transcriptase led to immortalization of these T cells, without altering the phenotype and without loss of specificity or functionality. As the T cells remained dependent on cytokines and Ag stimulation for their in vitro expansion, we conclude that immortalization was achieved without malignant transformation.
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CITATION STYLE
Hooijberg, E., Ruizendaal, J. J., Snijders, P. J. F., Kueter, E. W. M., Walboomers, J. M. M., & Spits, H. (2000). Immortalization of Human CD8+ T Cell Clones by Ectopic Expression of Telomerase Reverse Transcriptase. The Journal of Immunology, 165(8), 4239–4245. https://doi.org/10.4049/jimmunol.165.8.4239
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