FLASH Irradiation Regulates IFN-β induction by mtDNA via Cytochrome c Leakage
Lv, J.; Sun, J.; Luo, Y.; Liu, J.; Wu, D.; Fang, Y.; Lan, H.; Diao, L.; Ma, Y.; Li, Y.; Wang, M.; Zhao, Z.; Wang, H.; Morris, A.; Zhang, W.; Zhang, Z.; Lin, L.; Jia, H.; Wang, C.; Li, T.; Mourou, G.; Huang, S.; Yang, G.; Yan, X.
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Ultrahigh dose rate radiotherapy (FLASH-RT) is under intensive investigation for its biological benefits. The mechanisms underlying its ability to spare normal tissues while suppress tumor growth still remain controversial. Here we reveal that compared to the low dose rate electron irradiation (0.36 Gy/s), FLASH electron irradiation at 61 or 610 Gy/s enhances the cytochrome c leakage from mitochondria in human breast cells MCF-10A, which elicits substantial caspase activation, suppresses both the cytosolic mitochondrial DNA (mtDNA) accumulation and IFN-{beta} secretion. Besides, the deletion of mtDNA severely decreases the radiation-induced cGAS-STING activation. Conversely, the cytochrome c leakage in carcinoma cells MDA-MB-231 post electron irradiation is limited, especially for the case of FLASH irradiation, resulting in less cytosolic cytochrome c but stronger cGAS-STING activation than those in MCF-10A cells. The enhanced difference of cytochrome c leakage between cancer cells and normal cells post FLASH irradiation indicates a potential mechanism of FLASH effect by regulating the apoptotic and inflammatory pathway.
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