Iron Metabolism and Ferroptosis in Diabetic Kidney Disease

IF 2.7 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Fangxin Mu, Ping Luo, Yuexin Zhu, Ping Nie, Bing Li, Xue Bai
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引用次数: 0

Abstract

Diabetic kidney disease (DKD) is a major diabetic microvascular complication that still lacks effective therapeutic drugs. Ferroptosis is a recently identified form of programmed cell death that is triggered by iron overload. It is characterized by unrestricted lipid peroxidation and subsequent membrane damage and is found in various diseases. Accumulating evidence has highlighted the crucial roles of iron overload and ferroptosis in DKD. Here, we review iron metabolism and the biology of ferroptosis. The role of aberrant ferroptosis in inducing diverse renal intrinsic cell death, oxidative stress, and renal fibrosis in DKD is summarized, and we elaborate on critical regulatory factors related to ferroptosis in DKD. Finally, we focused on the significance of ferroptosis in the treatment of DKD and highlight recent data regarding the novel activities of some drugs as ferroptosis inhibitors in DKD, aiming to provide new research targets and treatment strategies on DKD.

Abstract Image

Abstract Image

Abstract Image

糖尿病肾病的铁代谢与铁下垂
糖尿病肾病(DKD)是一种主要的糖尿病微血管并发症,目前仍缺乏有效的治疗药物。铁中毒是最近发现的一种程序性细胞死亡形式,由铁超载引发。它的特点是无限制的脂质过氧化和随后的膜损伤,可在多种疾病中发现。越来越多的证据凸显了铁超载和铁变态反应在 DKD 中的关键作用。在此,我们回顾了铁代谢和铁变态反应的生物学过程。我们总结了在 DKD 中异常的铁蛋白沉积在诱导多种肾脏固有细胞死亡、氧化应激和肾脏纤维化中的作用,并阐述了与 DKD 中铁蛋白沉积相关的关键调控因素。最后,我们重点探讨了铁蛋白沉积在 DKD 治疗中的意义,并着重介绍了一些药物作为铁蛋白沉积抑制剂在 DKD 中的新活性,旨在为 DKD 提供新的研究靶点和治疗策略。
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来源期刊
Cell Biochemistry and Function
Cell Biochemistry and Function 生物-生化与分子生物学
CiteScore
6.20
自引率
0.00%
发文量
93
审稿时长
6-12 weeks
期刊介绍: Cell Biochemistry and Function publishes original research articles and reviews on the mechanisms whereby molecular and biochemical processes control cellular activity with a particular emphasis on the integration of molecular and cell biology, biochemistry and physiology in the regulation of tissue function in health and disease. The primary remit of the journal is on mammalian biology both in vivo and in vitro but studies of cells in situ are especially encouraged. Observational and pathological studies will be considered providing they include a rational discussion of the possible molecular and biochemical mechanisms behind them and the immediate impact of these observations to our understanding of mammalian biology.
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