Xu Wan-Xue, Wen Xue, Fu Yi-Tong, Yang Jie, Cui Han, Fan Rui-Feng
College of Veterinary Medicine, Shandong Agricultural University, 7 Panhe Street, Tai'an, 271017, Shandong, China.
Shandong Provincial Key Laboratory of Zoonoses, Shandong Agricultural University, 7 Panhe Street, Tai'an, 271017, Shandong, China.
Arch Toxicol. 2025 Apr;99(4):1257-1270. doi: 10.1007/s00204-025-03963-y. Epub 2025 Feb 10.
Nuclear receptor coactive 4 (NCOA4) is a specific receptor for ferritinophagy, transporting ferritin to lysosomal degradation, releasing free iron, and excessive iron levels may lead to cellular redox imbalance, contributing to cell death, predominantly ferroptosis. NCOA4 is regulated by a variety of transcriptional, post-transcriptional, translational, and post-translational modifications. Targeted modulation of NCOA4-mediated ferritinophagy has been successfully used as a therapeutic strategy in several disease models. Recent evidences have elucidated that ferritinophagy and ferroptosis played a major role in heavy metals toxicity. In this review, we explored the regulatory mechanism of NCOA4 as the sole receptor for ferritinophagy from multiple perspectives based on previous studies. The significant role of ferritinophagy-mediated ferroptosis in heavy metals toxicity was discussed in detail, emphasizing the great potential of NCOA4 as a target for heavy metals toxicity.
核受体共激活因子4(NCOA4)是铁蛋白自噬的特异性受体,将铁蛋白转运至溶酶体进行降解,释放游离铁,而铁水平过高可能导致细胞氧化还原失衡,促使细胞死亡,主要是铁死亡。NCOA4受多种转录、转录后、翻译和翻译后修饰的调控。在多种疾病模型中,对NCOA4介导的铁蛋白自噬进行靶向调节已成功用作一种治疗策略。最近的证据表明,铁蛋白自噬和铁死亡在重金属毒性中起主要作用。在本综述中,我们基于以往研究从多个角度探讨了NCOA4作为铁蛋白自噬唯一受体的调控机制。详细讨论了铁蛋白自噬介导的铁死亡在重金属毒性中的重要作用,强调了NCOA4作为重金属毒性靶点的巨大潜力。