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NCOA4介导的铁自噬在健康与疾病中的作用

The Role of NCOA4-Mediated Ferritinophagy in Health and Disease.

作者信息

Santana-Codina Naiara, Mancias Joseph D

机构信息

Division of Genomic Stability and DNA Repair, Department of Radiation Oncology, Dana-Farber Cancer Institute, Harvard Institute of Medicine, Room 221, 4 Blackfan Circle, Boston, MA 02215, USA.

出版信息

Pharmaceuticals (Basel). 2018 Oct 23;11(4):114. doi: 10.3390/ph11040114.

Abstract

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.

摘要

核受体辅激活因子4(NCOA4)是一种选择性货物受体,介导铁蛋白(“铁蛋白自噬”)的自噬降解,铁蛋白是一种胞质铁储存复合物。NCOA4介导的铁蛋白自噬通过根据需求促进铁蛋白铁的储存或释放来维持细胞内铁稳态。铁蛋白自噬参与铁依赖性生理过程,如红细胞生成,其中NCOA4介导铁蛋白铁释放用于线粒体血红素合成。最近,铁蛋白自噬已被证明可调节铁死亡,铁死亡是一种新描述的由过量脂质过氧化介导的铁依赖性细胞死亡形式。铁代谢和铁死亡的失调已在神经退行性疾病、癌症和感染中被描述,但关于铁蛋白自噬在这些疾病发病机制中的作用知之甚少。在这里,我们将综述NCOA4的生化调节、其对生理过程的贡献及其在疾病中的作用。最后,我们将讨论激活或抑制铁蛋白自噬和铁死亡用于治疗目的的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f28/6316710/7e0f076ec56e/pharmaceuticals-11-00114-g001.jpg

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