Iron Metabolism and Chelation Program, Discipline of Pathology, University of Sydney, NSW 2006, Australia.
Proc Natl Acad Sci U S A. 2010 Jun 15;107(24):10775-82. doi: 10.1073/pnas.0912925107. Epub 2010 May 21.
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.
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。