Medical Science and Technology Innovation Center, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, Shandong, 250117, China.
Iron Metabolism Laboratory, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, 4006, Australia.
Cell Death Dis. 2022 Jan 10;13(1):40. doi: 10.1038/s41419-021-04490-1.
Iron is vital for many physiological functions, including energy production, and dysregulated iron homeostasis underlies a number of pathologies. Ferroptosis is a recently recognized form of regulated cell death that is characterized by iron dependency and lipid peroxidation, and this process has been reported to be involved in multiple diseases. The mechanisms underlying ferroptosis are complex, and involve both well-described pathways (including the iron-induced Fenton reaction, impaired antioxidant capacity, and mitochondrial dysfunction) and novel interactions linked to cellular energy production. In this review, we examine the contribution of iron to diverse metabolic activities and their relationship to ferroptosis. There is an emphasis on the role of iron in driving energy production and its link to ferroptosis under both physiological and pathological conditions. In conclusion, excess reactive oxygen species production driven by disordered iron metabolism, which induces Fenton reaction and/or impairs mitochondrial function and energy metabolism, is a key inducer of ferroptosis.
铁对于许多生理功能至关重要,包括能量产生,而铁稳态的失调是许多病理的基础。铁死亡是一种新发现的细胞死亡形式,其特征是铁依赖性和脂质过氧化,据报道,这一过程涉及多种疾病。铁死亡的机制很复杂,既包括描述明确的途径(包括铁诱导的芬顿反应、抗氧化能力受损和线粒体功能障碍),也包括与细胞能量产生有关的新的相互作用。在这篇综述中,我们研究了铁对不同代谢活动的贡献及其与铁死亡的关系。重点是铁在生理和病理条件下驱动能量产生及其与铁死亡的关系。总之,铁代谢紊乱导致的活性氧(ROS)过度产生,引发芬顿反应和/或损害线粒体功能和能量代谢,是铁死亡的关键诱导因素。