SOD2
超氧化物歧化酶
癌症研究
福克斯O1
活性氧
干细胞
祖细胞
SOD1
造血干细胞
氧化应激
细胞生物学
骨髓
DNA损伤
造血
蛋白激酶B
生物
化学
药理学
免疫学
信号转导
生物化学
DNA
作者
Yan Qi,Shilei Chen,Yukai Lu,Zihao Zhang,Song Wang,Naicheng Chen,Mingqiang Shen,Fang Chen,Mo Chen,Yong Quan,Lijing Yang,Yang Xu,Yongping Su,Mengjia Hu,Junping Wang
标识
DOI:10.1016/j.freeradbiomed.2021.08.010
摘要
Ionizing radiation (IR)-induced excessive reactive oxygen species (ROS) is an important contributor of the injury of hematopoietic system. Grape seed proanthocyanidin extract (GSPE) is a new type of antioxidant, whereas whether it could ameliorate IR-induced hematopoietic injury remains unclear. Here, we show that GSPE treatment improves the survival of irradiated mice and alleviates IR-induced myelosuppression. Meanwhile, the hematopoietic reconstituting ability of hematopoietic stem cells (HSCs) in mice following irradiation exposure is significantly increased after GSPE treatment. Furthermore, GSPE treatment can reduce IR-induced ROS production and relieve DNA damage and apoptosis in hematopoietic stem progenitor cells (HSPCs). Interestingly, we find that a critical antioxidant-associated gene fokhead box transcription factor O1 (Foxo1) is significantly decreased in HSPCs after irradiation. Consistently, hematopoietic specific deletion of Foxo1 increases the radiosensitivity of mice. Further investigations reveal that GSPE treatment specifically upregulates the expression of Foxo1, as well as its target genes superoxide dismutase 1 (SOD1), superoxide dismutase 2 (SOD2) and catalase (CAT). Importantly, Foxo1 deficiency largely abolishes the radioprotection of GSPE on HSPCs. Collectively, our data demonstrate that GSPE plays an important role in ameliorating IR-induced HSPC injury via the Foxo1-mediated pathway. Therefore, GSPE may be used as a promising radioprotective agent.
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