Suppression of mitochondrial permeability transition pore and induction of lymphoma P388 cell death by cyclosporin A

被引:0
|
作者
Teplova, V [1 ]
Evtodienko, Y [1 ]
Odinokova, I [1 ]
Kruglov, A [1 ]
Kudrjavtsev, A [1 ]
机构
[1] RAS, Inst Theoret & Expt Biophys, Pushchino 142290, Moscow Region, Russia
关键词
apoptosis; cyclosporins; lymphoma cells; mitochondria; permeability transition pore; reactive oxygen species;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Suppression of the mitochondrial permeability transition pore (PTP) and induction of lymphoma P388 cell death were studied in the presence of cyclosporin A (CsA) and its derivatives. In experiments with permeabilized P388 cells, CsA and its nonimmunosuppressive derivative N-methyl-Val-4-CsA, but not cyclosporin H (CsH), enhanced Ca2+ accumulation in mitochondria and suppressed PTP opening. Moreover, CsA was able either itself to induce or to enhance a prooxidant-induced P388 programmed cell death. Blebbing and formation of apoptotic bodies were among the observed CsA effects. N-Methyl-Val-4-CsA showed similar effects, but CsH had no effect on P388 cell death, These results show that initial-stage P388 tumour cell death is not related to PTP opening but can be the result of PTP closing with a corresponding increase in the formation of reactive oxygen species.
引用
收藏
页码:75 / 80
页数:6
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