Department of Biology, University of Padova, 35121 Padova, Italy; Venetian Institute of Molecular Medicine, 35129 Padova, Italy.
Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305, USA.
Cell Metab. 2018 Apr 3;27(4):886-897.e4. doi: 10.1016/j.cmet.2018.02.018.
How intracellular pathogens acquire essential non-diffusible host metabolites and whether the host cell counteracts the siphoning of these nutrients by its invaders are open questions. Here we show that host mitochondria fuse during infection by the intracellular parasite Toxoplasma gondii to limit its uptake of fatty acids (FAs). A combination of genetics and imaging of FA trafficking indicates that Toxoplasma infection triggers lipophagy, the autophagy of host lipid droplets (LDs), to secure cellular FAs essential for its proliferation. Indeed, Toxoplasma FA siphoning and growth are reduced in host cells genetically deficient for autophagy or triglyceride depots. Conversely, Toxoplasma FA uptake and proliferation are increased in host cells lacking mitochondrial fusion, required for efficient mitochondrial FA oxidation, or where mitochondrial FA oxidation is pharmacologically inhibited. Thus, mitochondrial fusion can be regarded as a cellular defense mechanism against intracellular parasites, by limiting Toxoplasma access to host nutrients liberated by lipophagy.
细胞内病原体如何获取必需的不可扩散的宿主代谢物,以及宿主细胞是否会对抗其入侵者对这些营养物质的虹吸,这些都是悬而未决的问题。在这里,我们表明,在感染细胞内寄生虫刚地弓形虫时,宿主线粒体融合,以限制其对脂肪酸 (FA) 的摄取。对 FA 运输的遗传学和成像组合表明,刚地弓形虫感染会引发脂噬作用,即宿主脂滴 (LD) 的自噬,以确保其增殖所需的细胞内 FA。事实上,在自噬或甘油三酯库遗传缺陷的宿主细胞中,刚地弓形虫的 FA 虹吸和生长减少。相反,在缺乏线粒体融合的宿主细胞中,刚地弓形虫 FA 的摄取和增殖增加,而线粒体融合对于有效的线粒体 FA 氧化是必需的,或者在线粒体 FA 氧化被药物抑制的情况下。因此,线粒体融合可以被视为一种细胞防御机制,对抗通过脂噬作用释放的宿主营养物质的细胞内寄生虫。