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

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.

Automated summary

Mitochondrial oxidative damage is rapidly induced in hematopoietic stem cells (HSCs) after exposure to ionizing radiation, leading to apoptosis. The induction of 5-lipoxygenase (5-LOX) plays a key role in this process, while the natural antioxidant caffeic acid (CA) can protect against HSC apoptosis by suppressing 5-LOX-mediated mitochondrial oxidative damage.