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

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

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was analyzed. We found out that, in the site of infection, B-1a cells are activated very<br />

early after infection (within 12 hours) and in this time B cells relatively broad spectrum of<br />

cytokines. Thus, considering the protective efficacy of circulating antibodies, production<br />

of cytokines, and potent antigen-presenting function of B cells, B cell-mediated, as well<br />

as T cell-mediated immunity plays an equivalent role in control of F. tularensis infection<br />

in mice.<br />

Acknowledgement<br />

The authors are supported by the grant from Grant Agency of Czech Republic No.<br />

P302/11/1631<br />

P15. SENSITIZATION OF CELLS TOWARDS ANTICANCER TREATMENT BY INHIBITORS OF<br />

SUCCINATE DEHYDROGENASE<br />

Björn Kruspig 1 , Belma Skender 2,3 , Boris Zhivotovsky 1 , and Vladimir Gogvadze 1<br />

1<br />

Institute of Environmental Medicine, Division of Toxicology, Karolinska Institutet, Box<br />

210, Stockholm, SE-171 77 Sweden<br />

2<br />

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

Republic, v.v.i., Královopolská 135, 612 65 Brno, Czech Republic<br />

3<br />

Department of Animal Physiology and Immunology, Institute of Experimental Biology,<br />

Faculty of Science, Masaryk University, Terezy Novákové 64, 621 00 Brno, Czech<br />

Republic<br />

Cancer and apoptosis are regarded as antagonistic processes. Apoptosis may be<br />

involved in spontaneous regression of tumors, whereas defects in apoptotic pathways<br />

may contribute to tumor progression and resistance to treatment. Therefore, the<br />

stimulation of cell death is the most widely used tools in cancer therapy. Considering<br />

mitochondria as key participants in various forms of cell death steps directed to<br />

mitochondrial destabilization, permeabilization of the outer mitochondrial membrane<br />

(OMM) and release of pro-apoptotic proteins represent a promising strategy in fighting<br />

cancer. Mitochondria are multifunctional organelles, playing different vital roles in<br />

cell metabolism, survival and death. One of their essential physiological functions is<br />

the generation of ATP for metabolic demands through the oxidative phosphorylation<br />

(OXPHOS) pathway. They are also known as a major site of reactive oxygen species (ROS)<br />

production, which participates in different signaling pathways, but might cause cell<br />

damage if produced excessively. In addition, mitochondria are involved in intracellular<br />

Ca 2+ homeostasis regulation. All these functions of mitochondria are essential for cell<br />

survival and also play an important role in cell death stimulation, thus making these<br />

organelles an attractive target for cancer therapy.<br />

In the present work we analyzed possible consequences of combined treatment of<br />

tumor cells with inhibitors of succinate dehydrogenase (complex II of the mitochondrial<br />

respiratory chain) – thenoyltrifluoroacetone (TTFA) and methyl-malonate (MM) – in<br />

combination with the conventionally used anticancer drug cisplatin.<br />

Incubation of neuroblastoma Tet21N and SK-N-BE(2) cells with 5 µg/ml cisplatin for 24<br />

Analytical Cytometry VII 105

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