Faculty of Science, Yamagata University, Japan.
Faculty of Life Sciences, Kyoto Sangyo University, Japan.
FEBS J. 2021 May;288(10):3285-3299. doi: 10.1111/febs.15657. Epub 2020 Dec 30.
Most phospholipids are synthesised in the endoplasmic reticulum and distributed to other cellular membranes. Although the vesicle transport contributes to the phospholipid distribution among the endomembrane system, exactly how phospholipids are transported to, from and between mitochondrial membranes remains unclear. To gain insights into phospholipid transport routes into mitochondria, we expressed the Escherichia coli phosphatidylserine (PS) synthase PssA in various membrane compartments with distinct membrane topologies in yeast cells lacking a sole PS synthase (Cho1). Interestingly, PssA could complement loss of Cho1 when targeted to the endoplasmic reticulum (ER), peroxisome, or lipid droplet membranes. Synthesised PS could be converted to phosphatidylethanolamine (PE) by Psd1, the mitochondrial PS decarboxylase, suggesting that phospholipids synthesised in the peroxisomes and low doses (LDs) can efficiently reach mitochondria. Furthermore, we found that PssA which has been integrated into the mitochondrial inner membrane (MIM) from the matrix side could partially complement the loss of Cho1. The PS synthesised in the MIM was also converted to PE, indicating that PS flops across the MIM to become PE. These findings expand our understanding of the intracellular phospholipid transport routes via mitochondria.
大多数磷脂在内质网中合成,并分布到其他细胞膜中。尽管囊泡运输有助于在内质网系统中分配磷脂,但磷脂如何运输到线粒体膜、从线粒体膜运输以及在它们之间运输仍然不清楚。为了深入了解磷脂进入线粒体的运输途径,我们在缺乏单一磷脂合酶(Cho1)的酵母细胞中,用具有不同膜拓扑结构的各种膜区室表达大肠杆菌磷脂酰丝氨酸(PS)合酶 PssA。有趣的是,当 PssA 靶向内质网(ER)、过氧化物酶体或脂滴膜时,它可以弥补 Cho1 的缺失。由线粒体 PS 脱羧酶 Psd1 合成的 PS 可以转化为磷脂酰乙醇胺(PE),表明在过氧化物体和低剂量(LDs)中合成的磷脂可以有效地到达线粒体。此外,我们发现从基质侧整合到线粒体内膜(MIM)中的 PssA 可以部分弥补 Cho1 的缺失。在线粒体 MIM 中合成的 PS 也被转化为 PE,表明 PS 翻转穿过 MIM 成为 PE。这些发现扩展了我们对通过线粒体的细胞内磷脂运输途径的理解。