CD4+ and γδTCR+ T lymphocytes are sources of interleukin-17 in swine
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
22321808
DOI
10.1016/j.cyto.2012.01.004
PII: S1043-4666(12)00019-1
Knihovny.cz E-zdroje
- MeSH
- aktivace lymfocytů účinky léků MeSH
- CD4-pozitivní T-lymfocyty účinky léků imunologie MeSH
- DNA primery MeSH
- interleukin-17 biosyntéza genetika MeSH
- messenger RNA genetika MeSH
- polymerázová řetězová reakce s reverzní transkripcí MeSH
- prasata MeSH
- průtoková cytometrie MeSH
- receptory antigenů T-buněk gama-delta imunologie MeSH
- sekvence nukleotidů MeSH
- tetradekanoylforbolacetát farmakologie MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- DNA primery MeSH
- interleukin-17 MeSH
- messenger RNA MeSH
- receptory antigenů T-buněk gama-delta MeSH
- tetradekanoylforbolacetát MeSH
In the veterinary field, only limited information is available about interleukin-17A (IL-17), despite the fact that this cytokine plays an important role during pro-inflammatory immune responses and induces the production of chemotactic factors for neutrophils. The aim of this study was to characterize porcine IL-17-producing cells. We tested the cross-reactivity of five anti-human IL-17 monoclonal antibodies because such antibodies against porcine IL-17 are currently unavailable. Whole blood cells (WBCs) were stimulated with phorbol-myristate-acetate (PMA) and ionomycin and subsequently analyzed by flow cytometry. The antibody clone SCPL1362 was found to cross-react with porcine IL-17, whereas the other four antibodies tested did not recognize this cytokine. Using this antibody, we characterized porcine WBC-secreting IL-17 after PMA and ionomycin stimulation. All IL-17-producing WBCs were positive for the T lymphocyte marker CD3. Myeloid cells (CD172α(+)) and B lymphocytes (CD79α(+)) were IL-17 negative. The major subset of IL-17 positive T lymphocytes was the CD4(+) lymphocytes (about 60% of all IL-17 positive WBCs). The remaining IL-17 positive WBCs were γδTCR(+) lymphocytes. CD8 positive and CD8 negative cells were found within both CD4(+) and γδTCR(+) cells producing the cytokine. Moreover, IL-17 positive cells were mostly CD45RA negative, therefore activated cells or memory cells. Flow cytometry data were confirmed using sorted cells. Both sorted CD4(+) and γδTCR(+) cells produced IL-17 at mRNA level after PMA and ionomycin stimulation while double negative CD4(-)γδTCR(-) cells were negative for IL-17. We can conclude that only two subpopulations of porcine WBCs are sources of IL-17 after non-specific stimulation: CD3(+)CD4(+) and CD3(+)γδTCR(+).
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