The role of iron in mitochondrial function

被引:156
作者
Levi, Sonia [1 ,2 ]
Rovida, Ermanna [3 ]
机构
[1] Univ Vita Salute San Raffaele, I-20132 Milan, Italy
[2] Ist Sci San Raffaele, I-20132 Milan, Italy
[3] CNR, Inst Biomed Technol, Milan, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2009年 / 1790卷 / 07期
关键词
Mitochondria; Iron; Iron-sulfur cluster; Heme; Mitochondria iron overload diseases; LINKED SIDEROBLASTIC ANEMIA; SULFUR PROTEIN MATURATION; FRIEDREICH ATAXIA; HEME-SYNTHESIS; CLUSTER BIOGENESIS; SUCCINATE-DEHYDROGENASE; FRATAXIN DEFICIENCY; FERRITIN EXPRESSION; OXIDATIVE STRESS; HELA-CELLS;
D O I
10.1016/j.bbagen.2008.09.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Iron is an essential element for life, as it is a cofactor for enzymes involved in many metabolic processes, but it can also be harmful, since its excess is thought to enhance the production of reactive oxygen species and induce oxidative damage. Iron is transformed into its biologically available form in the mitochondrion by the iron-sulfur (Fe/S) cluster and heme synthesis pathways. During the past decade, substantial progress has been made in the elucidation of iron-linked mechanisms that occur in the mitochondrion, demonstrating the crucial role played by this organelle in maintaining cellular iron homeostasis. General Significance: This review summarizes current knowledge of the mechanisms underlying iron trafficking in mitochondria and how it is handled inside the organelle. Relevant updates with regard to the Fe/S cluster and heme biosynthetic pathways, as well as the relationship between mitochondrial iron homeostasis impairment and related diseases, are also discussed. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:629 / 636
页数:8
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