-
Something wrong with this record ?
Relative expression of γδ T-cell receptor gene families detected by RT-PCR and capillary electrophoresis
L. Tesarova, I. Koutna, M. Dvorakova, M. Klabusay
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
NS9681
MZ0
CEP Register
NS9671
MZ0
CEP Register
Digital library NLK
Full text - Article
Full text - Article
Source
Source
NLK
Medline Complete (EBSCOhost)
from 2005-02-01 to 1 year ago
Wiley Online Library (archiv)
from 1997-01-01 to 2012-12-31
- MeSH
- Time Factors MeSH
- Adult MeSH
- Electrophoresis, Capillary methods MeSH
- Hematologic Neoplasms genetics pathology MeSH
- Leukocytes, Mononuclear cytology metabolism MeSH
- Middle Aged MeSH
- Humans MeSH
- Multigene Family * MeSH
- Reverse Transcriptase Polymerase Chain Reaction methods MeSH
- Receptors, Antigen, T-Cell, gamma-delta genetics metabolism MeSH
- Oligonucleotide Array Sequence Analysis methods MeSH
- Case-Control Studies MeSH
- T-Lymphocytes cytology metabolism MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't 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
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc13012717
- 003
- CZ-PrNML
- 005
- 20151026083145.0
- 007
- ta
- 008
- 130404s2012 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1111/j.1744-313x.2012.01114.x $2 doi
- 035 __
- $a (PubMed)22486991
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Tesarova, L $u 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
- 245 10
- $a Relative expression of γδ T-cell receptor gene families detected by RT-PCR and capillary electrophoresis / $c L. Tesarova, I. Koutna, M. Dvorakova, M. Klabusay
- 520 9_
- $a 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.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a studie případů a kontrol $7 D016022
- 650 _2
- $a elektroforéza kapilární $x metody $7 D019075
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a hematologické nádory $x genetika $x patologie $7 D019337
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a leukocyty mononukleární $x cytologie $x metabolismus $7 D007963
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 12
- $a multigenová rodina $7 D005810
- 650 _2
- $a sekvenční analýza hybridizací s uspořádaným souborem oligonukleotidů $x metody $7 D020411
- 650 _2
- $a receptory antigenů T-buněk gama-delta $x genetika $x metabolismus $7 D016692
- 650 _2
- $a polymerázová řetězová reakce s reverzní transkripcí $x metody $7 D020133
- 650 _2
- $a T-lymfocyty $x cytologie $x metabolismus $7 D013601
- 650 _2
- $a časové faktory $7 D013997
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Koutna, I $u Centre for Biomedical Image Analysis, Faculty of Informatics, Masaryk University, Brno, Czech Republic
- 700 1_
- $a Dvorakova, M $u Centre for Biomedical Image Analysis, Faculty of Informatics, Masaryk University, Brno, Czech Republic
- 700 1_
- $a Klabusay, M $u International Clinical Research Center - ICCT, St. Anne's University Hospital Brno, Brno, Czech Republic
- 773 0_
- $w MED00008484 $t International journal of immunogenetics $x 1744-313X $g Roč. 39, č. 5 (2012), s. 381-8
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/22486991 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y 4 $z 0
- 990 __
- $a 20130404 $b ABA008
- 991 __
- $a 20151026083147 $b ABA008
- 999 __
- $a ok $b bmc $g 975915 $s 810998
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2012 $b 39 $c 5 $d 381-8 $i 1744-313X $m International journal of immunogenetics $n Int J Immunogen $x MED00008484
- GRA __
- $a NS9681 $p MZ0
- GRA __
- $a NS9671 $p MZ0
- LZP __
- $a Pubmed-20130404