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