Mechanism of cell death by 5‐aminolevulinic acid‐based photodynamic action and its enhancement by ferrochelatase inhibitors in human histiocytic lymphoma cell line U937 |
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Authors: | Takashi Amo Noriaki Kawanishi Masataka Uchida Hirofumi Fujita Eri Oyanagi Toshihiko Utsumi Tetsuya Ogino Keiji Inoue Taro Shuin Kozo Utsumi Junzo Sasaki |
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Affiliation: | 1. Department of Cytology and Histology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan;2. Department of Health and Sports Science, Kawasaki University of Medical Welfare, Matsushima, Kurashiki, Japan;3. Department of Biological Chemistry, Faculty of Agriculture, Yamaguchi University,Yamaguchi, Japan;4. Department of Pathology and Experimental Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan;5. Department of Urology, Kochi University Medical School, Nankoku, Kochi, Japan |
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Abstract: | Photodynamic therapy (PDT) for tumors is based on the tumor‐selective accumulation of a photosensitizer, protoporphyrin IX (PpIX), followed by irradiation with visible light. However, the molecular mechanism of cell death caused by PDT has not been fully elucidated. The 5‐aminolevulinic acid (ALA)‐based photodynamic action (PDA) was dependent on the accumulation of PpIX, the level of which decreased rapidly by eliminating ALA from the incubation medium in human histiocytic lymphoma U937 cells. PDA induced apoptosis characterized by lipid peroxidation, increase in Bak and Bax/Bcl‐xL, decrease in Bid, membrane depolarization, cytochrome c release, caspase‐3 activation, phosphatidylserine (PS) externalization. PDT‐induced cell death seemed to occur predominantly via apoptosis through distribution of PpIX in mitochondria. These cell death events were enhanced by ferrochelatase inhibitors. These results indicated that ALA‐based‐PDA induced apoptotic cell death through a mitochondrial pathway and that ferrochelatase inhibitors might enhanced the effect of PDT for tumors even at low concentrations of ALA. Copyright © 2009 John Wiley & Sons, Ltd. |
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Keywords: | 5‐aminolevulinic acid apoptosis ferrochelatase protoporphyrin IX photodynamic therapy U937 cell |
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