Browsing by Author "Todorovic-Markovic, Biljana (6602608361)"
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Publication Modulation of tumor necrosis factor-mediated cell death by fullerenes(2008) ;Harhaji, Ljubica (6507652139) ;Isakovic, Aleksandra (57202555421) ;Vucicevic, Ljubica (35333082000) ;Janjetovic, Kristina (35332184000) ;Misirkic, Maja (35332620200) ;Markovic, Zoran (34968401700) ;Todorovic-Markovic, Biljana (6602608361) ;Nikolic, Nadezda (12809125700) ;Vranjes-Djuric, Sanja (12809584300) ;Nikolic, Zoran (7006320528)Trajkovic, Vladimir (7004516866)Purpose. The fullerene (C60/C70 mixture-C 60/70) nanocrystalline suspension prepared by solvent exchange method using tetrahydrofyran (THF/nC60/70) and polyhydroxylated C 60/70 [C60/70(OH)n] were compared for their ability to modulate cytotoxicity of the proinflammatory cytokine tumor necrosis factor (TNF). Materials and Methods. TNF-induced cytotoxicity was assessed in L929 fibrosarcoma cells by crystal violet assay. The type of cell death (apoptosis/necrosis), production of reactive oxygen species, mitochondrial depolarization and caspase activation were determined by flow cytometry using the appropriate reporter dyes. Results. THF/nC60/70 augmented, while C60/70(OH) n reduced the cytotoxicity of TNF. The numbers of cells undergoing apoptosis/necrosis, as well as of those displaying the activation of apoptosis-inducing enzymes of caspase family, were respectively increased or reduced by THF/nC60/70 or C60/70(OH) n. The antioxidant N-acetylcysteine and mitochondrial permeability transition inhibitor cyclosporin A each partly blocked the cytotoxic action of TNF, indicating the involvement of oxidative stress and mitochondrial dysfunction in the TNF cytotoxicity. Accordingly, THF/nC60/70 or C60/70(OH)n potentiated or suppressed, respectively, TNF-triggered oxidative stress and mitochondrial depolarization. Conclusion. The ability of different fullerene preparations to modulate TNF-induced oxidative stress and subsequent cell death suggests their potential value in the TNF-based cancer therapy or prevention of TNF-dependent tissue damage. © 2007 Springer Science+Business Media, LLC. - Some of the metrics are blocked by yourconsent settings
Publication Modulation of tumor necrosis factor-mediated cell death by fullerenes(2008) ;Harhaji, Ljubica (6507652139) ;Isakovic, Aleksandra (57202555421) ;Vucicevic, Ljubica (35333082000) ;Janjetovic, Kristina (35332184000) ;Misirkic, Maja (35332620200) ;Markovic, Zoran (34968401700) ;Todorovic-Markovic, Biljana (6602608361) ;Nikolic, Nadezda (12809125700) ;Vranjes-Djuric, Sanja (12809584300) ;Nikolic, Zoran (7006320528)Trajkovic, Vladimir (7004516866)Purpose. The fullerene (C60/C70 mixture-C 60/70) nanocrystalline suspension prepared by solvent exchange method using tetrahydrofyran (THF/nC60/70) and polyhydroxylated C 60/70 [C60/70(OH)n] were compared for their ability to modulate cytotoxicity of the proinflammatory cytokine tumor necrosis factor (TNF). Materials and Methods. TNF-induced cytotoxicity was assessed in L929 fibrosarcoma cells by crystal violet assay. The type of cell death (apoptosis/necrosis), production of reactive oxygen species, mitochondrial depolarization and caspase activation were determined by flow cytometry using the appropriate reporter dyes. Results. THF/nC60/70 augmented, while C60/70(OH) n reduced the cytotoxicity of TNF. The numbers of cells undergoing apoptosis/necrosis, as well as of those displaying the activation of apoptosis-inducing enzymes of caspase family, were respectively increased or reduced by THF/nC60/70 or C60/70(OH) n. The antioxidant N-acetylcysteine and mitochondrial permeability transition inhibitor cyclosporin A each partly blocked the cytotoxic action of TNF, indicating the involvement of oxidative stress and mitochondrial dysfunction in the TNF cytotoxicity. Accordingly, THF/nC60/70 or C60/70(OH)n potentiated or suppressed, respectively, TNF-triggered oxidative stress and mitochondrial depolarization. Conclusion. The ability of different fullerene preparations to modulate TNF-induced oxidative stress and subsequent cell death suggests their potential value in the TNF-based cancer therapy or prevention of TNF-dependent tissue damage. © 2007 Springer Science+Business Media, LLC.
