1. Hyperthermia and tumour necrosis factor-alpha induced apoptosis via mitochondrial damage.
- Author
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Yuen WF, Fung KP, Lee CY, Choy YM, Kong SK, Ko S, and Kwok TT
- Subjects
- Animals, Blotting, Western, Cell Line, Cyclosporine pharmacology, Cytochrome c Group metabolism, Cytosol drug effects, Cytosol enzymology, Fluorescein-5-isothiocyanate, Fluorescent Dyes, Immunosuppressive Agents pharmacology, Membranes drug effects, Membranes metabolism, Mice, Mitochondria ultrastructure, Tetrazolium Salts, Thiazoles, Tumor Necrosis Factor-alpha antagonists & inhibitors, Apoptosis drug effects, Fever pathology, Mitochondria drug effects, Tumor Necrosis Factor-alpha toxicity
- Abstract
Hyperthermia is a potential anti-cancer regimen but the mode of action is far from clear. Based on the flow cytometric analysis with FITC-annexin V and propidium iodide, apoptosis was found to be the major form of cell death after the treatment with hyperthermia (43 degrees C, 3 h) and/or recombinant murine tumour necrosis factor-alpha (TNF-alpha, 50 ng/ml) in L929 cells. Since mitochondria are thought to play a key role in apoptosis, experiments were done to assess their role in the hyperthermia-mediated apoptosis. Our results indicate that hyperthermia was able to depolarize the mitochondrial membrane potential (delta psi m) and release cytochrome c to the cytoplasm, in a way very similar to the action of TNF-alpha. With the use of cyclosporin A to inhibit the delta psi m dissipation, the cytotoxicity mediated by hyperthermia or TNF-alpha was suppressed. Taken together, our results indicate that hyperthermia and TNF-alpha can induce apoptosis in L929 cells and the mitochondrial dysfunction plays a key role in the cell death process.
- Published
- 2000
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