Assessing T Lymphocyte Aging Using Telomere Length and Telomerase Activity Measurements in Low Cell Numbers.
Cell Culture Techniques
/ instrumentation
DNA
/ isolation & purification
Enzyme Assays
/ instrumentation
HEK293 Cells
Humans
Real-Time Polymerase Chain Reaction
/ instrumentation
Single-Cell Analysis
/ instrumentation
T-Lymphocyte Subsets
/ physiology
Telomerase
/ metabolism
Telomere
/ genetics
Telomere Shortening
/ physiology
Single cell
T lymphocytes
Telomerase activity
Telomere length
qPCR
Journal
Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969
Informations de publication
Date de publication:
2019
2019
Historique:
entrez:
10
8
2019
pubmed:
10
8
2019
medline:
23
6
2020
Statut:
ppublish
Résumé
As T lymphocytes proliferate and differentiate in vivo or in vitro, their functional capacity can change dramatically. In particular, extensive cell division is often associated with telomere shortening and the onset of cellular senescence, thus impacting the proliferative potential of the cells. Telomere length and integrity represent therefore key molecular markers of the status and aging of the cells. To assess these markers, we established qPCR-based methods to measure telomere length as well as telomerase activity, applied to low cell numbers, which is necessary when working with rare or small subsets of T lymphocytes.
Identifiants
pubmed: 31396941
doi: 10.1007/978-1-4939-9728-2_18
doi:
Substances chimiques
DNA
9007-49-2
Telomerase
EC 2.7.7.49
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM