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Vestn Ross Akad Med Nauk ; (8): 3-6, 2011.
Artigo em Russo | MEDLINE | ID: mdl-21950128

RESUMO

rTNFalpha-induced programmed death of Jurkat tumor cells cultured with 17-AAG, a selective inhibitor of heat shock protein (Hsp90), was studied by fluorescent microscopy with the use of FITC-labeled annexin V and propidium iodide. Caspase-3 and -8 activities were determined by spectrophotometry using a caspase- 3 and -8 colorimetric assay kit. It was shown that inhibition of Hsp90 leads to activation of Jurkat cell apoptosis while Hsp90 itself suppresses this process. 17-AAG enhances rTNFa-induced apoptosis of tumor cells.


Assuntos
Apoptose/efeitos dos fármacos , Benzoquinonas/metabolismo , Caspase 3 , Caspase 8 , Proteínas de Choque Térmico HSP90/metabolismo , Lactamas Macrocíclicas/metabolismo , Fator de Necrose Tumoral alfa/metabolismo , Anexina A5/metabolismo , Apoptose/fisiologia , Caspase 3/análise , Caspase 3/metabolismo , Caspase 8/análise , Caspase 8/metabolismo , Inibidores Enzimáticos/metabolismo , Fluoresceína-5-Isotiocianato , Corantes Fluorescentes , Humanos , Células Jurkat , Microscopia de Fluorescência , Propídio , Espectrofotometria
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