Caffeic acid attenuates irradiation-induced hematopoietic stem cell apoptosis through inhibiting mitochondrial damage

被引:17
|
作者
Wang, Xinmiao [1 ]
Liao, Weinian [1 ]
Chen, Jun [1 ]
Wu, Yiding [1 ]
Liu, Chaonan [1 ]
Chen, Shilei [1 ]
Xu, Yang [1 ]
Wang, Song [1 ]
Su, Yongping [1 ]
Du, Changhong [1 ]
Wang, Junping [1 ]
机构
[1] Army Med Univ, State Key Lab Trauma Burns & Combined Injury, Inst Combined Injury,Coll Prevent Med, Chongqing Engn Res Ctr Nanomed,Third Mil Med Univ, Chongqing 400038, Peoples R China
关键词
Caffeic acid; Hematopoietic stem cell; Irradiation; Mitochondrial damage; ROS; IONIZING-RADIATION; OXIDATIVE STRESS;
D O I
10.1016/j.yexcr.2021.112934
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hematopoietic stem cells (HSCs) are sensitive to ionizing radiation (IR) damage, and its injury is the primary cause of bone marrow (BM) hematopoietic failure and even death after exposure to a certain dose of IR. However, the underlying mechanisms remain incompletely understood. Here we show that mitochondrial oxidative damage, which is characterized by mitochondrial reactive oxygen species overproduction, mitochondrial membrane potential reduction and mitochondrial permeability transition pore opening, is rapidly induced in both human and mouse HSCs and directly accelerates HSC apoptosis after IR exposure. Mechanistically, 5-lipoxygenase (5-LOX) is induced by IR exposure and contributes to IR-induced mitochondrial oxidative damage through inducing lipid peroxidation. Intriguingly, a natural antioxidant, caffeic acid (CA), can attenuate IRinduced HSC apoptosis through suppressing 5-LOX-mediated mitochondrial oxidative damage, thus protecting against BM hematopoietic failure after IR exposure. These findings uncover a critical role for mitochondria in IRinduced HSC injury and highlight the therapeutic potential of CA in BM hematopoietic failure induced by IR.
引用
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页数:10
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