Mitochondrial iron homeostasis and its dysfunctions in neurodegenerative disorders

被引:126
作者
Mena, Natalia P.
Urrutia, Pamela J.
Lourido, Fernanda
Carrasco, Carlos M.
Nunez, Marco T.
机构
[1] Univ Chile, Fac Ciencias, Dept Biol, Santiago 7800024, Chile
[2] Univ Chile, Res Ring Oxidat Stress Nervous Syst, Santiago 7800024, Chile
关键词
Mitochondrial iron homeostasis; Iron-sulfur cluster; Heme; Reactive oxygen species; Neurodegenerative disease; AMYLOID PRECURSOR PROTEIN; LINKED SIDEROBLASTIC ANEMIA; FREE-RADICAL GENERATION; HUNTINGTONS-DISEASE; ALZHEIMERS-DISEASE; OXIDATIVE STRESS; COMPLEX-I; FRIEDREICHS-ATAXIA; SUBSTANTIA-NIGRA; BRAIN IRON;
D O I
10.1016/j.mito.2015.02.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Synthesis of the iron-containing prosthetic groups heme and iron-sulfur clusters occurs in mitochondria. The mitochondrion is also an important producer of reactive oxygen species (ROS), which are derived from electrons leaking from the electron transport chain. The coexistence of both ROS and iron in the secluded space of the mitochondrion makes this organelle particularly prone to oxidative damage. Here, we review the elements that configure mitochondrial iron homeostasis and discuss the principles of iron-mediated ROS generation in mitochondria. We also review the evidence for mitochondrial dysfunction and iron accumulation in Alzheimer's disease, Huntington Disease, Friedreich's ataxia, and in particular Parkinson's disease. We postulate that a positive feedback loop of mitochondrial dysfunction, iron accumulation, and ROS production accounts for the process of cell death in various neurodegenerative diseases in which these features are present. (C) 2015 Elsevier B.V. and Mitochondria Research Society. All rights reserved.
引用
收藏
页码:92 / 105
页数:14
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