Grape seed proanthocyanidin extract ameliorates ionizing radiation-induced hematopoietic stem progenitor cell injury by regulating Foxo1 in mice

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
出处
期刊:Free Radical Biology and Medicine [Elsevier]
卷期号:174: 144-156 被引量:18
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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