铁蛋白
神经退行性变
细胞生物学
胞浆
细胞内
自噬
脂质过氧化
线粒体
核受体
铁转运蛋白
生物
化学
新陈代谢
疾病
生物化学
细胞凋亡
氧化应激
医学
铁稳态
内科学
酶
基因
转录因子
作者
Naiara Santana-Codina,Joseph D. Mancias
出处
期刊:Pharmaceuticals
[Multidisciplinary Digital Publishing Institute]
日期:2018-10-23
卷期号:11 (4): 114-114
被引量:256
摘要
Nuclear receptor coactivator 4 (NCOA4) is a selective cargo receptor that mediates the autophagic degradation of ferritin (“ferritinophagy”), the cytosolic iron storage complex. NCOA4-mediated ferritinophagy maintains intracellular iron homeostasis by facilitating ferritin iron storage or release according to demand. Ferritinophagy is involved in iron-dependent physiological processes such as erythropoiesis, where NCOA4 mediates ferritin iron release for mitochondrial heme synthesis. Recently, ferritinophagy has been shown to regulate ferroptosis, a newly described form of iron-dependent cell death mediated by excess lipid peroxidation. Dysregulation of iron metabolism and ferroptosis have been described in neurodegeneration, cancer, and infection, but little is known about the role of ferritinophagy in the pathogenesis of these diseases. Here, we will review the biochemical regulation of NCOA4, its contribution to physiological processes and its role in disease. Finally, we will discuss the potential of activating or inhibiting ferritinophagy and ferroptosis for therapeutic purposes.
科研通智能强力驱动
Strongly Powered by AbleSci AI