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ABSTRACTS – ORAL PRESENTATIONS - AMCA, spol. s r.o.

ABSTRACTS – ORAL PRESENTATIONS - AMCA, spol. s r.o.

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(Broad Institute, Boston MA). Ag-activated cells spread<br />

on fibronectin whereas upon PGE 2<br />

stimulation the<br />

cells created F-Actin rich protrusions. Cell area was<br />

determined and normalized to non-activated cells (D).<br />

At least 300 cells were evaluated in each condition.<br />

Means ±SD were calculated from duplicates in one<br />

representative experiment. Bars 20 mm.<br />

<strong>ABSTRACTS</strong> – POSTERS<br />

P1. NITRO-OLEIC ACID ATTENUATES THE INNATE IMMUNE RESPONSES OF<br />

MACROPHAGES STIMULATED WITH BACTERIAL ENDOTOXIN<br />

Gabriela Ambrozova 1,2 , Lukas Kubala 1,2 , Tanja K. Rudolph 3 , Antonin Lojek 1 , Thorben<br />

Ravekes 3 , Michaela Pekarova 1<br />

1<br />

Institute of Biophysics AS CR, Brno, Czech Republic; ambrozova@ibp.cz<br />

2<br />

ICRC/FNUSA, Brno, Czech Republic;<br />

3<br />

Hamburg University Heart Center, Hamburg, Germany<br />

Nitrated fatty acids (NO 2<br />

-FAs) represent a novel group of pluripotent signalling molecules,<br />

endogenously generated as an adaptive response of organism to oxidative stress (Baker<br />

et al., 2009). NO 2<br />

-FAs were shown to exert significant anti-inflammatory signalling action<br />

in immune and vascular models and so are hypothesized as protective compounds that<br />

can effectively down regulate ineligible activation of innate immune cells, particularly<br />

professional phagocytes (Trostchansky and Rubbo, 2008). Protective effects of NO 2<br />

-FAs<br />

on severe diseases including pulmonary hypertension and atherosclerosis have been<br />

described (Rudolph et al., 2010). Nevertheless, detailed mechanisms of their action in<br />

regulation of innate immune responses are not completely understood. Therefore, we<br />

investigated the role and mechanism of action of nitro-oleic acid (OANO 2<br />

) in endotoxinstimulated<br />

RAW 264.7 macrophages.<br />

Our results showed that OANO 2<br />

prevented the endotoxin-induced activation of<br />

macrophages in a dose-dependent manner. It was able to down-regulate phagocytic<br />

capability, production of reactive oxygen and nitrogen species as well as inflammatory<br />

cytokines. Importantly, changes in the production of inflammatory mediators were<br />

associated with reduction of endotoxin-induced MAPK activation and expression of NF-<br />

Analytical Cytometry VII 87

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