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Measuring Telomerase Activity in Senescent Human T Cells Upon Genetic Modification

Abstract:
Telomerase, a RNA-dependent DNA polymerase that adds telomeric DNA at the 3′ ends of eukaryotic chromosomes, is essential for the lifelong preservation of the proliferative potential of antigen specific T lymphocytes. However, senescent T cells that have low telomerase activity, short telomeres and lack of replicative capacity accumulate in old humans, patients with chronic viral infections and cancer. The mechanisms inhibiting telomerase in these cells are poorly understood. Here I describe a strategy that was successfully applied to identify pathways causing telomerase dysfunction in primary human senescent T lymphocytes. Such strategy couples lentiviral vector-based gene manipulations to functional and signaling readouts directly ex vivo, in humans.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1007/978-1-4939-6548-9_10

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Institution:
University of Oxford
Division:
MSD
Department:
NDORMS
Sub department:
Kennedy Institute for Rheumatology
Role:
Author


Publisher:
Springer New York
Journal:
Methods Molecular Biology More from this journal
Volume:
1514
Pages:
119-126
Publication date:
2016-10-28
Acceptance date:
2016-10-28
DOI:
EISSN:
1940-6029
ISSN:
1064-3745


Keywords:
Pubs id:
pubs:656002
UUID:
uuid:7ffed93c-25b5-4025-9cb2-345a434e978c
Local pid:
pubs:656002
Source identifiers:
656002
Deposit date:
2016-10-31

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