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共同特征引发线粒体自噬/异源吞噬相互作用。

Common Traits Spark the Mitophagy/Xenophagy Interplay.

作者信息

Singh Aarti, Kendall Sharon L, Campanella Michelangelo

机构信息

Department of Comparative Biomedical Sciences, Royal Veterinary College, London, United Kingdom.

Department of Pathology and Pathogen Biology, Royal Veterinary College, Hertfordshire, United Kingdom.

出版信息

Front Physiol. 2018 Sep 20;9:1172. doi: 10.3389/fphys.2018.01172. eCollection 2018.

Abstract

Selective autophagy contributes to the wellbeing of eukaryotic cells by recycling cellular components, disposing damaged organelles, and removing pathogens, amongst others. Both the process of selective mitochondrial autophagy (Mitophagy) and the of intracellular pathogen-engulfment (Xenophagy) are facilitated via protein assemblies which have shared molecules, a prime example being the Tank-Binding Kinase 1 (TBK1). TBK1 plays a central role in the immunity response driven by Xenophagy and was recently shown to be an amplifying mechanism in Mitophagy, bring to attention the potential cross talk between the two processes. Here we draw parallels between Xenophagy and Mitophagy, speculating on the inhibitory mechanisms of specific proteins (e.g., the 18 kDa protein TSPO), how the preferential sequestering toward one of the two pathways may undermine the other, and in this way impair cellular response to pathogens and cellular immunity. We believe that an in depth understanding of the commonalities may present an opportunity to design novel therapeutic strategies targeted at both the autonomous and non-autonomous processes of selective autophagy.

摘要

选择性自噬通过回收细胞成分、处理受损细胞器以及清除病原体等方式,对真核细胞的健康状态起到促进作用。选择性线粒体自噬(线粒体自噬)过程和细胞内病原体吞噬(异噬)过程均通过具有共享分子的蛋白质组装体得以促进,其中一个主要例子是 Tank 结合激酶 1(TBK1)。TBK1 在异噬驱动的免疫反应中发挥核心作用,最近还被证明是线粒体自噬中的一种放大机制,这引发了人们对这两个过程之间潜在相互作用的关注。在此,我们对异噬和线粒体自噬进行比较,推测特定蛋白质(如 18 kDa 蛋白质 TSPO)的抑制机制,以及偏向于这两个途径之一的优先隔离如何可能损害另一个途径,进而损害细胞对病原体的反应和细胞免疫。我们认为,深入了解这些共性可能为设计针对选择性自噬的自主和非自主过程的新型治疗策略提供契机。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d3f/6158333/56412e0401aa/fphys-09-01172-g001.jpg

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