Reichert Cadiele Oliana, de Freitas Fábio Alessandro, Sampaio-Silva Juliana, Rokita-Rosa Leonardo, Barros Priscila de Lima, Levy Debora, Bydlowski Sérgio Paulo
Lipids, Oxidation, and Cell Biology Group, Laboratory of Immunology (LIM19), Heart Institute (InCor), Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo 05403-900, Brazil.
Instituto Nacional de Ciencia e Tecnologia em Medicina Regenerativa (INCT-Regenera), CNPq, Rio de Janeiro 21941-902, Brazil.
Int J Mol Sci. 2020 Nov 20;21(22):8765. doi: 10.3390/ijms21228765.
Ferroptosis is a type of cell death that was described less than a decade ago. It is caused by the excess of free intracellular iron that leads to lipid (hydro) peroxidation. Iron is essential as a redox metal in several physiological functions. The brain is one of the organs known to be affected by iron homeostatic balance disruption. Since the 1960s, increased concentration of iron in the central nervous system has been associated with oxidative stress, oxidation of proteins and lipids, and cell death. Here, we review the main mechanisms involved in the process of ferroptosis such as lipid peroxidation, glutathione peroxidase 4 enzyme activity, and iron metabolism. Moreover, the association of ferroptosis with the pathophysiology of some neurodegenerative diseases, namely Alzheimer's, Parkinson's, and Huntington's diseases, has also been addressed.
铁死亡是一种在不到十年前才被描述的细胞死亡类型。它是由细胞内游离铁过量导致脂质(氢)过氧化引起的。铁作为一种氧化还原金属在多种生理功能中至关重要。大脑是已知受铁稳态平衡破坏影响的器官之一。自20世纪60年代以来,中枢神经系统中铁浓度的增加一直与氧化应激、蛋白质和脂质氧化以及细胞死亡有关。在此,我们综述了铁死亡过程中涉及的主要机制,如脂质过氧化、谷胱甘肽过氧化物酶4酶活性和铁代谢。此外,还探讨了铁死亡与某些神经退行性疾病(即阿尔茨海默病、帕金森病和亨廷顿病)病理生理学的关联。