Center for Cardiovascular Research and Alternative Medicine, University of Wyoming College of Health Sciences, Laramie, WY 82071, USA.
University of Visayas, Gullas College of Medicine, Dionisio Jakosalem St, Cebu City, 6000, Cebu, Philippines.
Trends Endocrinol Metab. 2021 Jul;32(7):444-462. doi: 10.1016/j.tem.2021.04.010. Epub 2021 May 15.
Ferroptosis is a form of regulated cell death modality associated with disturbed iron-homeostasis and unrestricted lipid peroxidation. Ample evidence has depicted an essential role for ferroptosis as either the cause or consequence for human diseases, denoting the likely therapeutic promises for targeting ferroptosis in the preservation of human health. Ferritinophagy, a selective form of autophagy, contributes to the initiation of ferroptosis through degradation of ferritin, which triggers labile iron overload (IO), lipid peroxidation, membrane damage, and cell death. In this review, we will delineate the role of ferritinophagy in ferroptosis, and its underlying regulatory mechanisms, to unveil the therapeutic value of ferritinophagy as a target in the combat of ferroptosis to manage metabolic diseases.
铁死亡是一种与铁稳态紊乱和不受限制的脂质过氧化有关的受调控的细胞死亡方式。大量证据表明,铁死亡作为人类疾病的原因或结果具有重要作用,这表明靶向铁死亡在保护人类健康方面具有潜在的治疗前景。铁蛋白自噬是一种选择性自噬形式,通过降解铁蛋白引发不稳定铁过载 (IO)、脂质过氧化、膜损伤和细胞死亡,从而促进铁死亡的发生。在这篇综述中,我们将阐述铁蛋白自噬在铁死亡中的作用及其潜在的调控机制,揭示铁蛋白自噬作为治疗靶点在对抗铁死亡以治疗代谢性疾病方面的治疗价值。