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pubmed-article:15341925pubmed:abstractTextThe mechanism of cell death by pheophorbide a (Pba) which has been established to be a potential photosensitizer was examined in experimental photodynamic therapy (PDT) on Jurkat cells, a human lymphoid tumor cell line. In 30-60 min after irradiation, Pba treated cells exhibited apoptotic features including membrane blebbing and DNA fragmentation. Pba/PDT caused a rapid release of cytochrome c from mitochondria into the cytosol. Sequentially, activation of caspase-3 and the cleavage of poly ADP-ribose polymerase (PARP) were followed. Meanwhile, no evidence of activation of caspase-8 was indicated in the cells. In experiments with caspase inhibitors, it was found that caspase-3 alone was sufficient initiator for the Pba-induced apoptosis of the cells. Pba specific emission spectra were confirmed in the mitochondrial fraction and the light irradiation caused a rapid change in its membrane potential. Thus, mitochondria were entailed as the crucial targets for Pba as well as a responsible component for the cytochrome c release to initiate apoptotic pathways. Taken together, it was concluded that the mode of Jurkat cell death by Pba/PDT is an apoptosis, which is initiated by mitochondrial cytochrome c release and caspase-3-pathways.lld:pubmed
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pubmed-article:15341925pubmed:pagination119-26lld:pubmed
pubmed-article:15341925pubmed:dateRevised2007-7-23lld:pubmed
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pubmed-article:15341925pubmed:articleTitlePhotoactivation of pheophorbide a induces a mitochondrial-mediated apoptosis in Jurkat leukaemia cells.lld:pubmed
pubmed-article:15341925pubmed:affiliationDepartment of Microbiology, College of Medicine, Yonsei University, CPO Box 8044, Seoul 120-752, Republic of Korea.lld:pubmed
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pubmed-article:15341925pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:15341925pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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