线粒体
生物发生
胞浆
细胞生物学
铁硫簇
血红素
生物化学
线粒体生物发生
生物
化学
酶
基因
作者
Jonathan V. Dietz,Jennifer L. Fox,Oleh Khalimonchuk
出处
期刊:Cells
[MDPI AG]
日期:2021-08-25
卷期号:10 (9): 2198-2198
被引量:41
标识
DOI:10.3390/cells10092198
摘要
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.
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