-
Je něco špatně v tomto záznamu ?
Multiparametric flow cytometry analysis of peripheral blood B cell trafficking differences among Epstein-Barr virus infected and uninfected subpopulations
K. Zachova, P. Kosztyu, J. Zadrazil, K. Matousovic, K. Vondrak, P. Hubacek, K. Kostovcikova, H. Tlaskalova Hogenova, J. Mestecky, M. Raska
Jazyk angličtina Země Česko
Typ dokumentu srovnávací studie, časopisecké články
NLK
Directory of Open Access Journals
od 2001
Free Medical Journals
od 1998
Medline Complete (EBSCOhost)
od 2007-06-01
ROAD: Directory of Open Access Scholarly Resources
od 2001
PubMed
31723302
DOI
10.5507/bp.2019.052
Knihovny.cz E-zdroje
- MeSH
- B-lymfocyty imunologie MeSH
- dospělí MeSH
- infekce virem Epsteina-Barrové imunologie patofyziologie MeSH
- krev imunologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- průtoková cytometrie MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- vezikulární transportní proteiny imunologie metabolismus MeSH
- zdraví dobrovolníci pro lékařské studie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- srovnávací studie MeSH
AIMS: Epstein-Barr virus (EBV) targets predominantly B cells and these cells could acquire new phenotype characteristics. Here we analyzed whether EBV-infected and -uninfected B cells from healthy subjects differ in proportion of dominant phenotypes, maturation stage, and homing receptors expression. METHODS: EBV-infected and -uninfected cells were identified by flow cytometry using fluorophore-labeled EBV RNA-specific DNA probes combined with fluorophore-labeled antibody to surface lineage markers, integrins, chemokine receptors, and immunoglobulin isotypes, including intracellular ones. RESULTS: Our results show that the trafficking characteristics of EBERpos B cells are distinct from EBERneg B cells with most dominant differences detected for α4β1 and α4β7 and CCR5 and CCR7. EBV-positive cells are predominantly memory IgM+ B cells or plasmablasts/plasma cells (PB/PC) positive for IgA or less for IgM. In comparison to uninfected B cells, less EBV-positive B cells express α4β7 and almost no cells express α4β1. EBV-positive B cells contained significantly higher proportion of CCR5+ and CCR7+ cells in comparison to EBV-negative cells. In vitro exposure of blood mononuclear cells to pro-inflammatory cytokine IL-6 reduces population of EBV-positive B cell. CONCLUSION: Although EBV-infected B cells represent only a minor subpopulation, their atypical functions could contribute in predisposed person to development abnormities such as some autoimmune diseases or tumors. Using multi-parameter flow cytometry we characterized differences in migration of EBV-positive and -negative B cells of various maturation stage and isotype of produced antibodies particularly different targeting to mucosal tissues of gastrointestinal and respiratory tracts.
Department of Medicine University of Alabama at Birmingham Birmingham Alabama USA
Department of Microbiology University of Alabama at Birmingham Birmingham Alabama USA
Citace poskytuje Crossref.org
Literatura
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21021183
- 003
- CZ-PrNML
- 005
- 20210916103934.0
- 007
- ta
- 008
- 210806s2020 xr d f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.5507/bp.2019.052 $2 doi
- 035 __
- $a (PubMed)31723302
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Zachová, Kateřina $7 xx0253002 $u Department of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic
- 245 10
- $a Multiparametric flow cytometry analysis of peripheral blood B cell trafficking differences among Epstein-Barr virus infected and uninfected subpopulations / $c K. Zachova, P. Kosztyu, J. Zadrazil, K. Matousovic, K. Vondrak, P. Hubacek, K. Kostovcikova, H. Tlaskalova Hogenova, J. Mestecky, M. Raska
- 504 __
- $a Literatura
- 520 9_
- $a AIMS: Epstein-Barr virus (EBV) targets predominantly B cells and these cells could acquire new phenotype characteristics. Here we analyzed whether EBV-infected and -uninfected B cells from healthy subjects differ in proportion of dominant phenotypes, maturation stage, and homing receptors expression. METHODS: EBV-infected and -uninfected cells were identified by flow cytometry using fluorophore-labeled EBV RNA-specific DNA probes combined with fluorophore-labeled antibody to surface lineage markers, integrins, chemokine receptors, and immunoglobulin isotypes, including intracellular ones. RESULTS: Our results show that the trafficking characteristics of EBERpos B cells are distinct from EBERneg B cells with most dominant differences detected for α4β1 and α4β7 and CCR5 and CCR7. EBV-positive cells are predominantly memory IgM+ B cells or plasmablasts/plasma cells (PB/PC) positive for IgA or less for IgM. In comparison to uninfected B cells, less EBV-positive B cells express α4β7 and almost no cells express α4β1. EBV-positive B cells contained significantly higher proportion of CCR5+ and CCR7+ cells in comparison to EBV-negative cells. In vitro exposure of blood mononuclear cells to pro-inflammatory cytokine IL-6 reduces population of EBV-positive B cell. CONCLUSION: Although EBV-infected B cells represent only a minor subpopulation, their atypical functions could contribute in predisposed person to development abnormities such as some autoimmune diseases or tumors. Using multi-parameter flow cytometry we characterized differences in migration of EBV-positive and -negative B cells of various maturation stage and isotype of produced antibodies particularly different targeting to mucosal tissues of gastrointestinal and respiratory tracts.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a senioři nad 80 let $7 D000369
- 650 _2
- $a B-lymfocyty $x imunologie $7 D001402
- 650 _2
- $a krev $x imunologie $7 D001769
- 650 _2
- $a infekce virem Epsteina-Barrové $x imunologie $x patofyziologie $7 D020031
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a průtoková cytometrie $7 D005434
- 650 _2
- $a zdraví dobrovolníci pro lékařské studie $7 D064368
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a vezikulární transportní proteiny $x imunologie $x metabolismus $7 D033921
- 655 _2
- $a srovnávací studie $7 D003160
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Kosztyu, Petr $7 xx0239748 $u Department of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic
- 700 1_
- $a Zadražil, Josef, $d 1954- $7 xx0074493 $u Department of Internal Medicine III - Nephrology, Rheumatology and Endocrinology, Palacky University Olomouc and University Hospital Olomouc, Czech Republic
- 700 1_
- $a Matoušovic, Karel, $d 1940-2021 $7 jn19990216123 $u Department of Internal Medicine, 2nd Faculty Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic
- 700 1_
- $a Vondrák, Karel $7 xx0260300 $u Department of Pediatrics, 2nd Faculty Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic
- 700 1_
- $a Hubáček, Petr, $d 1978- $7 xx0075829 $u Department of Microbiology, 2nd Faculty Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic
- 700 1_
- $a Kostovčíková, Klára $7 xx0264110 $u Laboratory of Cellular and Molecular Immunology, Institute of Microbiology, Czech Academy of Sciences, Prague, Czech Republic
- 700 1_
- $a Tlaskalová, Helena, $d 1938- $7 jn20000402365 $u Laboratory of Cellular and Molecular Immunology, Institute of Microbiology, Czech Academy of Sciences, Prague, Czech Republic
- 700 1_
- $a Městecký, Jiří, $d 1941- $7 nlk20050164024 $u Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA $u Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama, USA $u Laboratory of Cellular and Molecular Immunology, Institute of Microbiology, Czech Academy of Sciences, Prague, Czech Republic
- 700 1_
- $a Raška, Milan, $d 1967- $7 xx0060585 $u Department of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic $u Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama, USA
- 773 0_
- $w MED00012606 $t Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia $x 1213-8118 $g Roč. 164, č. 3 (2020), s. 247-254
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31723302 $y Pubmed
- 910 __
- $a ABA008 $b A 1502 $c 958 $y p $z 0
- 990 __
- $a 20210806 $b ABA008
- 991 __
- $a 20210916103931 $b ABA008
- 999 __
- $a ok $b bmc $g 1694790 $s 1141636
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2020 $b 164 $c 3 $d 247-254 $e 20191012 $i 1213-8118 $m Biomedical papers of the Medical Faculty of the University Palacký, Olomouc Czech Republic $n Biomed. Pap. Fac. Med. Palacký Univ. Olomouc Czech Repub. (Print) $x MED00012606
- LZP __
- $b NLK118 $a Pubmed-20210806