Metformin ameliorates ionizing irradiation-induced long-term hematopoietic stem cell injury in mice

作者：Guoshun Xu, Hongying Wu, Junling Zhang, Deguan Li, Yueying Wang, Yingying Wang, Heng Zhang, Lu Lu, Chengcheng Li, Song Huang, Yonghua Xing, Daohong Zhou, Aimin Meng · 发表于：Free Radical Biology and Medicine · 年份：2015 · DOI：10.1016/j.freeradbiomed.2015.05.045 · 被引用次数：127 · 研究领域：Metabolism, Diabetes, and Cancer、Effects of Radiation Exposure、Hematopoietic Stem Cell Transplantation

Exposure to ionizing radiation (IR) increases the production of reactive oxygen species (ROS) not only by the radiolysis of water but also through IR-induced perturbation of the cellular metabolism and disturbance of the balance of reduction/oxidation reactions. Our recent studies showed that the increased production of intracellular ROS induced by IR contributes to IR-induced late effects, particularly in the hematopoietic system, because inhibition of ROS production with an antioxidant after IR exposure can mitigate IR-induced long-term bone marrow (BM) injury. Metformin is a widely used drug for the treatment of type 2 diabetes. Metformin also has the ability to regulate cellular metabolism and ROS production by activating AMP-activated protein kinase. Therefore, we examined whether metformin can ameliorate IR-induced long-term BM injury in a total-body irradiation (TBI) mouse model. Our results showed that the administration of metformin significantly attenuated TBI-induced increases in ROS production and DNA damage and upregulation of NADPH oxidase 4 expression in BM hematopoietic stem cells (HSCs). These changes were associated with a significant increase in BM HSC frequency, a considerable improvement in in vitro and in vivo HSC function, and complete inhibition of upregulation of p16 Ink4a in HSCs after TBI. These findings demonstrate that metformin can attenuate TBI-induced long-term BM injury at least in part by inhibiting the induction of chronic oxidative stress i...