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本文引用的文献

1
A labile iron pool.不稳定铁池
J Biol Chem. 1946 Sep;165(1):397.
2
Human MRCKalpha is regulated by cellular iron levels and interferes with transferrin iron uptake.人 MRCKα 受细胞内铁水平调节,并干扰转铁蛋白铁摄取。
Biochem Biophys Res Commun. 2010 Apr 30;395(2):163-7. doi: 10.1016/j.bbrc.2010.02.148. Epub 2010 Feb 25.
3
Frataxin, a molecule of mystery: trading stability for function in its iron-binding site.铁蛋白,一个神秘的分子:在其铁结合部位,稳定性与功能之间的权衡。
Biochem J. 2010 Feb 9;426(2):e1-3. doi: 10.1042/BJ20091959.
4
Iron-sulfur proteins in health and disease.铁硫蛋白在健康与疾病中的作用。
Trends Endocrinol Metab. 2010 May;21(5):302-14. doi: 10.1016/j.tem.2009.12.006. Epub 2010 Jan 8.
5
The ins and outs of mitochondrial iron-loading: the metabolic defect in Friedreich's ataxia.线粒体铁加载的来龙去脉:弗里德里希共济失调的代谢缺陷。
J Mol Med (Berl). 2010 Apr;88(4):323-9. doi: 10.1007/s00109-009-0565-x. Epub 2009 Dec 9.
6
Frataxin interacts with Isu1 through a conserved tryptophan in its beta-sheet.铁蛋白通过其β-折叠中的保守色氨酸与 Isu1 相互作用。
Hum Mol Genet. 2010 Jan 15;19(2):276-86. doi: 10.1093/hmg/ddp495. Epub 2009 Nov 2.
7
Elucidation of the mechanism of mitochondrial iron loading in Friedreich's ataxia by analysis of a mouse mutant.通过对小鼠突变体的分析阐明弗里德赖希共济失调中线粒体铁负荷的机制。
Proc Natl Acad Sci U S A. 2009 Sep 22;106(38):16381-6. doi: 10.1073/pnas.0906784106. Epub 2009 Sep 4.
8
Abcb10 physically interacts with mitoferrin-1 (Slc25a37) to enhance its stability and function in the erythroid mitochondria.Abcb10与线粒体铁转运蛋白-1(Slc25a37)发生物理相互作用,以增强其在红系线粒体中的稳定性和功能。
Proc Natl Acad Sci U S A. 2009 Sep 22;106(38):16263-8. doi: 10.1073/pnas.0904519106. Epub 2009 Sep 4.
9
Iron sequestration and anemia of inflammation.铁螯合与炎症性贫血
Semin Hematol. 2009 Oct;46(4):387-93. doi: 10.1053/j.seminhematol.2009.06.001.
10
Discovery of genes essential for heme biosynthesis through large-scale gene expression analysis.通过大规模基因表达分析发现血红素生物合成所必需的基因。
Cell Metab. 2009 Aug;10(2):119-30. doi: 10.1016/j.cmet.2009.06.012.

线粒体铁转运和线粒体与细胞质之间铁代谢的整合。

Mitochondrial iron trafficking and the integration of iron metabolism between the mitochondrion and cytosol.

机构信息

Iron Metabolism and Chelation Program, Discipline of Pathology, University of Sydney, NSW 2006, Australia.

出版信息

Proc Natl Acad Sci U S A. 2010 Jun 15;107(24):10775-82. doi: 10.1073/pnas.0912925107. Epub 2010 May 21.

DOI:10.1073/pnas.0912925107
PMID:20495089
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2890738/
Abstract

The mitochondrion is well known for its key role in energy transduction. However, it is less well appreciated that it is also a focal point of iron metabolism. Iron is needed not only for heme and iron sulfur cluster (ISC)-containing proteins involved in electron transport and oxidative phosphorylation, but also for a wide variety of cytoplasmic and nuclear functions, including DNA synthesis. The mitochondrial pathways involved in the generation of both heme and ISCs have been characterized to some extent. However, little is known concerning the regulation of iron uptake by the mitochondrion and how this is coordinated with iron metabolism in the cytosol and other organelles (e.g., lysosomes). In this article, we discuss the burgeoning field of mitochondrial iron metabolism and trafficking that has recently been stimulated by the discovery of proteins involved in mitochondrial iron storage (mitochondrial ferritin) and transport (mitoferrin-1 and -2). In addition, recent work examining mitochondrial diseases (e.g., Friedreich's ataxia) has established that communication exists between iron metabolism in the mitochondrion and the cytosol. This finding has revealed the ability of the mitochondrion to modulate whole-cell iron-processing to satisfy its own requirements for the crucial processes of heme and ISC synthesis. Knowledge of mitochondrial iron-processing pathways and the interaction between organelles and the cytosol could revolutionize the investigation of iron metabolism.

摘要

线粒体以其在能量转导中的关键作用而闻名。然而,人们对其作为铁代谢的焦点却知之甚少。铁不仅是参与电子传递和氧化磷酸化的血红素和铁硫簇(ISC)蛋白所必需的,而且是细胞质和核内多种功能所必需的,包括 DNA 合成。线粒体生成血红素和 ISC 的途径已经在一定程度上得到了描述。然而,关于线粒体对铁的摄取的调节以及如何与细胞质和其他细胞器(例如溶酶体)中的铁代谢相协调,知之甚少。在本文中,我们讨论了线粒体铁代谢和运输的新兴领域,这一领域最近因参与线粒体铁储存(线粒体铁蛋白)和运输(mitoferrin-1 和 -2)的蛋白质的发现而得到了刺激。此外,最近对线粒体疾病(如弗里德里希共济失调症)的研究已经证实,线粒体和细胞质中的铁代谢之间存在着通讯。这一发现揭示了线粒体调节细胞内铁处理的能力,以满足其自身对血红素和 ISC 合成这两个关键过程的需求。线粒体铁处理途径和细胞器与细胞质之间的相互作用的知识可能会彻底改变对铁代谢的研究。