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Relative expression of γδ T-cell receptor gene families detected by RT-PCR and capillary electrophoresis
L. Tesarova, I. Koutna, M. Dvorakova, M. Klabusay
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
NS9681
MZ0
CEP - Centrální evidence projektů
NS9671
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Plný text - Článek
Zdroj
Zdroj
NLK
Medline Complete (EBSCOhost)
od 2005-02-01 do Před 1 rokem
Wiley Online Library (archiv)
od 1997-01-01 do 2012-12-31
- MeSH
- časové faktory MeSH
- dospělí MeSH
- elektroforéza kapilární metody MeSH
- hematologické nádory genetika patologie MeSH
- leukocyty mononukleární cytologie metabolismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- multigenová rodina * MeSH
- polymerázová řetězová reakce s reverzní transkripcí metody MeSH
- receptory antigenů T-buněk gama-delta genetika metabolismus MeSH
- sekvenční analýza hybridizací s uspořádaným souborem oligonukleotidů metody MeSH
- studie případů a kontrol MeSH
- T-lymfocyty cytologie metabolismus MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
γδ T cells are intensively studied because their function in infection, allergy, autoimmune disease, cancer and post-transplant period is not yet fully understood. PCR-based techniques were established to study the γ variable (Vγ) and δ variable (Vδ) gene families. PCR product evaluation is routinely carried out by Southern blot analysis or the third complementarity-determining region spectratyping, but a fast and simple assessment of Vγ and Vδ gene family expression is missing. The aim of our study was to test capillary electrophoresis as a potential method for evaluating the composition of the γδ T-cell population. This report provides optimized PCR conditions for γδ T-cell receptor amplification. Further, it describes the utilization of capillary electrophoresis in the Agilent 2100 Bioanalyzer to evaluate the relative expression of Vγ and Vδ gene families after their amplification. An application of the methodology to peripheral blood mononuclear cell samples from patients during haemato-oncological treatment is shown. The described methodology is fast and simple to operate and is therefore suitable as a first screening of the γδ T-cell population composition in tissues of interest.
Centre for Biomedical Image Analysis Faculty of Informatics Masaryk University Brno Czech Republic
International Clinical Research Center ICCT St Anne's University Hospital Brno Brno Czech Republic
Citace poskytuje Crossref.org
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