IL-10 does not affect oxidative burst and expression of selected surface antigen on human blood phagocytes in vitro
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
15046557
Knihovny.cz E-zdroje
- MeSH
- antigen Lewis X metabolismus MeSH
- antigeny CD11b metabolismus MeSH
- antigeny CD31 metabolismus MeSH
- časové faktory MeSH
- CD antigeny metabolismus MeSH
- fagocyty účinky léků metabolismus fyziologie MeSH
- interleukin-10 aplikace a dávkování farmakologie fyziologie MeSH
- interleukin-6 aplikace a dávkování farmakologie MeSH
- interleukin-8 aplikace a dávkování farmakologie MeSH
- L-selektin metabolismus MeSH
- leukocyty účinky léků metabolismus fyziologie MeSH
- lidé MeSH
- luminiscenční měření MeSH
- monocyty účinky léků metabolismus fyziologie MeSH
- neutrofily účinky léků metabolismus fyziologie MeSH
- průtoková cytometrie MeSH
- reaktivní formy kyslíku metabolismus MeSH
- respirační vzplanutí účinky léků fyziologie MeSH
- rhodaminy chemie MeSH
- tetradekanoylforbolacetát farmakologie MeSH
- TNF-alfa aplikace a dávkování farmakologie MeSH
- zymosan farmakologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antigen Lewis X MeSH
- antigeny CD11b MeSH
- antigeny CD31 MeSH
- CD antigeny MeSH
- dihydrorhodamine 123 MeSH Prohlížeč
- interleukin-10 MeSH
- interleukin-6 MeSH
- interleukin-8 MeSH
- L-selektin MeSH
- reaktivní formy kyslíku MeSH
- rhodaminy MeSH
- tetradekanoylforbolacetát MeSH
- TNF-alfa MeSH
- zymosan MeSH
Cytokines play a major role in the control of inflammatory responses, participate in the regulation of blood phagocyte activities and as such are used for immunomodulatory therapy. In the present study, the influence of IL-10 on human blood phagocyte activity in the presence/absence of IL-6, IL-8 and TNF-alpha was tested in vitro. Our research analyzed the effects of cytokines on the production of reactive oxygen species measured by chemiluminescence and flow cytometry, and on the expression of surface molecules (CD11b, CD15, CD62L, CD31) measured by flow cytometry. IL-10 had no inhibitory effect on reactive oxygen species production and the expression of any examined adhesion molecule by resting or stimulated blood phagocytes within 3 h of incubation. Conversely, TNF-alpha, IL-6, and IL-8 increased reactive oxygen species production and the expression of CD11b and CD15 on both neutrophils and monocytes and decreased the expression of CD62L. These priming effects of the tested pro-inflammatory cytokines were not affected by IL-10. The obtained results suggest that IL-10 does not directly control blood phagocyte activation. These results also provide better information about the contribution of IL-6, IL-8 and TNF-alpha to the regulation of blood phagocyte-mediated inflammatory processes.
The potency of hyaluronan of different molecular weights in the stimulation of blood phagocytes