Department of Biochemistry, University of Nebraska, Lincoln, NE 68588, USA.
Department of Chemistry and Biochemistry, College of Charleston, Charleston, SC 29424, USA.
Cells. 2021 Aug 25;10(9):2198. doi: 10.3390/cells10092198.
Cellular iron homeostasis and mitochondrial iron homeostasis are interdependent. Mitochondria must import iron to form iron-sulfur clusters and heme, and to incorporate these cofactors along with iron ions into mitochondrial proteins that support essential functions, including cellular respiration. In turn, mitochondria supply the cell with heme and enable the biogenesis of cytosolic and nuclear proteins containing iron-sulfur clusters. Impairment in cellular or mitochondrial iron homeostasis is deleterious and can result in numerous human diseases. Due to its reactivity, iron is stored and trafficked through the body, intracellularly, and within mitochondria via carefully orchestrated processes. Here, we focus on describing the processes of and components involved in mitochondrial iron trafficking and storage, as well as mitochondrial iron-sulfur cluster biogenesis and heme biosynthesis. Recent findings and the most pressing topics for future research are highlighted.
细胞内铁稳态和线粒体铁稳态是相互依存的。线粒体必须输入铁来形成铁硫簇和血红素,并将这些辅助因子与铁离子一起掺入支持基本功能的线粒体蛋白中,包括细胞呼吸。反过来,线粒体为细胞提供血红素,并使含有铁硫簇的胞质和核蛋白的生物发生成为可能。细胞内或线粒体铁稳态的损害是有害的,并可能导致许多人类疾病。由于其反应性,铁通过精心协调的过程在体内、细胞内和线粒体中储存和运输。在这里,我们重点描述线粒体铁运输和储存的过程和组成部分,以及线粒体铁硫簇生物发生和血红素生物合成。强调了最近的发现和未来研究的最紧迫课题。