Adenosine modulates LPS-induced cytokine production in porcine monocytes
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
23388525
DOI
10.1016/j.cyto.2012.12.026
PII: S1043-4666(13)00005-7
Knihovny.cz E-zdroje
- MeSH
- adenosin-5'-(N-ethylkarboxamid) farmakologie MeSH
- adenosin farmakologie MeSH
- agonisté purinergních receptorů P1 farmakologie MeSH
- antagonisté purinergního receptoru P1 farmakologie MeSH
- antigen CD163 MeSH
- antigeny diferenciační myelomonocytární metabolismus MeSH
- CD antigeny metabolismus MeSH
- cytokiny biosyntéza genetika MeSH
- lipopolysacharidy farmakologie MeSH
- messenger RNA genetika metabolismus MeSH
- monocyty účinky léků metabolismus MeSH
- purinergní receptory P1 genetika metabolismus MeSH
- receptory buněčného povrchu metabolismus MeSH
- regulace genové exprese účinky léků MeSH
- Sus scrofa metabolismus MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adenosin-5'-(N-ethylkarboxamid) MeSH
- adenosin MeSH
- agonisté purinergních receptorů P1 MeSH
- antagonisté purinergního receptoru P1 MeSH
- antigen CD163 MeSH
- antigeny diferenciační myelomonocytární MeSH
- CD antigeny MeSH
- cytokiny MeSH
- lipopolysacharidy MeSH
- messenger RNA MeSH
- purinergní receptory P1 MeSH
- receptory buněčného povrchu MeSH
Adenosine plays an important role during inflammation, particularly through modulation of monocyte function. The objective of the present study was to evaluate the effect of synthetic adenosine analogs on cytokine production by porcine monocytes. The LPS-stimulated cytokine production was measured by flow cytometry and quantitative real-time PCR. Adenosine receptor expression was measured by quantitative real-time PCR. The present study demonstrates that adenosine analog N-ethylcarboxyamidoadenosine (NECA) down-regulates TNF-α production and up-regulates IL-8 production by LPS-stimulated porcine monocytes. The effect was more pronounced in CD163(-) subset of monocytes compared to the CD163(+) subset. Although both monocyte subsets express mRNA for A1, A2A, A2B and A3 adenosine receptors, the treatment of monocytes with various adenosine receptor agonists and antagonists proved that the effect of adenosine is mediated preferentially via A2A adenosine receptor. Moreover, the study suggests that the effect of NECA on porcine monocytes alters the levels of the cytokines which could play a role in the differentiation of naive T cells into Th17 cells. The results suggest that adenosine plays an important role in modulation of cytokine production by porcine monocytes.
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