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

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

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that the interaction of MPO with glycocalyx GAGs can lead to collapse of the glycocalyx<br />

structure. In order to get an insight into the mechanism how MPO may affect this, MPO<br />

mediated modulation of viscosity of GAGs solution as a degree of modulation of GAG<br />

three dimensional structure was determined. Data show a remarkable MPO mediated<br />

increase of the viscosity of two model GAGs hyaluronate and chondroitin sulphate.<br />

Further, MPO mediated decrease of GAG intrinsic negative charge at physiological<br />

conditions was evaluated. Different experimental settings were tested to stabilize GAGs<br />

in three dimensional structures which allowed the determination of the charge change<br />

employing dyes alcian blue X8 or direct red. Results suggest that staining with both dyes<br />

corresponds in a linear manner to the amount of embedded GAGs and that cationic<br />

proteins decrease the overall charge of embedded GAGs. Interestingly, similar effect was<br />

observed in vivo in mouse after application of alcian blue into the carotid artery and<br />

consequent loss of staining after application of MPO.<br />

These findings extend the knowledge of MPO inflammatory properties in vascular<br />

inflammation.<br />

Acknowledgements<br />

This work was supported by grants from the Czech Science Foundation No. P305/12/<br />

J038 and from DFG BA1870/9-1; KL 2516/1-1 and the European Social Fund - Project<br />

OganoNET (CZ.1.07/2.4.00/31.0245) and HistoPARK (CZ.1.07/2.3.00/20.0185). LK was<br />

supported by the European Regional Development Fund - Project FNUSA-ICRC (No.<br />

CZ.1.05/1.1.00/02.0123).<br />

P17. ROSIGLITAZONE ACTS AS AN EFFICIENT MODULATOR OF LA-12-INDUCED<br />

CYTOTOXIC AND CYTOSTATIC RESPONSE OF COLON CANCER CELLS<br />

Jarmila Lauková 1,2,3 , Iva Jelínková 1,2 , Jiřina Hofmanová 1,2 , Nicol Straková 1,6 , Petr Sova 4 , Jiří<br />

Ehrmann 5 , Zdeněk Kolář 5 , Alois Kozubík 1,2 and Alena Hyršlová Vaculová 1,3<br />

1<br />

Department of Cytokinetics, Institute of Biophysics, Academy of Sciences of the Czech<br />

Republic, v.v..i., Brno, Czech Republic; laukova@ibp.cz, vaculova@ibp.cz<br />

2<br />

Institute of Experimental Biology, Faculty of Science, Masaryk University, Brno, Czech<br />

Republic<br />

3<br />

Center of Biomolecular and Cellular Engineering, International Clinical Research Center,<br />

St. Anne´s University Hospital Brno, Czech Republic<br />

4<br />

Platinum Pharmaceuticals, a.s., Brno, Czech Republic<br />

5<br />

Department of Clinical and Molecular Pathology, Faculty of Medicine and Dentistry,<br />

Palacky University Olomouc, Czech Republic<br />

Rosiglitazone, a synthetic ligand of peroxisome proliferator-activated receptor gamma<br />

(PPARgamma) can suppress proliferation and stimulate death of colon cancer cells.<br />

In addition, it may also act as an agent sensitizing the cancer cells to the action of<br />

selected chemotherapeutic drugs, which suggests its potential application in antitumor<br />

therapy. Our results showed that pretreatment of HCT116 human colon cancer cells<br />

with rosiglitazone resulted in enhancement of apoptosis induced by platinum (IV)<br />

Analytical Cytometry VII 107

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