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通过细菌毒素的视角看哺乳动物膜运输。

Mammalian membrane trafficking as seen through the lens of bacterial toxins.

机构信息

Global Health Institute, School of Life Sciences, EPFL, Lausanne, Switzerland.

出版信息

Cell Microbiol. 2020 Apr;22(4):e13167. doi: 10.1111/cmi.13167.

DOI:10.1111/cmi.13167
PMID:32185902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7154709/
Abstract

A fundamental question of eukaryotic cell biology is how membrane organelles are organised and interact with each other. Cell biologists address these questions by characterising the structural features of membrane compartments and the mechanisms that coordinate their exchange. To do so, they must rely on variety of cargo molecules and treatments that enable targeted perturbation, localisation, and labelling of specific compartments. In this context, bacterial toxins emerged in cell biology as paradigm shifting molecules that enabled scientists to not only study them from the side of bacterial infection but also from the side of the mammalian host. Their selectivity, potency, and versatility made them exquisite tools for uncovering much of our current understanding of membrane trafficking mechanisms. Here, we will follow the steps that lead toxins until their intracellular targets, highlighting how specific events helped us comprehend membrane trafficking and establish the fundamentals of various cellular organelles and processes. Bacterial toxins will continue to guide us in answering crucial questions in cellular biology while also acting as probes for new technologies and applications.

摘要

真核细胞生物学的一个基本问题是膜细胞器如何组织和相互作用。细胞生物学家通过描述膜隔室的结构特征以及协调它们交换的机制来解决这些问题。为此,他们必须依赖各种货物分子和处理方法,以实现特定隔室的靶向扰动、定位和标记。在这种情况下,细菌毒素在细胞生物学中脱颖而出,成为改变观念的分子,使科学家不仅能够从细菌感染的角度,也能够从哺乳动物宿主的角度来研究它们。它们的选择性、效力和多功能性使它们成为揭示我们目前对膜运输机制理解的极好工具。在这里,我们将按照毒素进入细胞内靶标的步骤进行,重点介绍特定事件如何帮助我们理解膜运输,并建立各种细胞细胞器和过程的基础。细菌毒素将继续指导我们回答细胞生物学中的关键问题,同时也作为新技术和应用的探针。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66af/7154709/621f392b5f50/CMI-22-e13167-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66af/7154709/621f392b5f50/CMI-22-e13167-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66af/7154709/621f392b5f50/CMI-22-e13167-g001.jpg

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本文引用的文献

1
Toxins Utilize the Endoplasmic Reticulum-Associated Protein Degradation Pathway in Their Intoxication Process.毒素在其中毒过程中利用内质网相关蛋白降解途径。
Int J Mol Sci. 2019 Mar 15;20(6):1307. doi: 10.3390/ijms20061307.
2
Anthrax toxin requires ZDHHC5-mediated palmitoylation of its surface-processing host enzymes.炭疽毒素需要 ZDHHC5 介导的表面处理宿主酶的棕榈酰化。
Proc Natl Acad Sci U S A. 2019 Jan 22;116(4):1279-1288. doi: 10.1073/pnas.1812588116. Epub 2019 Jan 4.
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Mechanisms protecting host cells against bacterial pore-forming toxins.
宿主细胞抵抗细菌成孔毒素的机制。
Cell Mol Life Sci. 2019 Apr;76(7):1319-1339. doi: 10.1007/s00018-018-2992-8. Epub 2018 Dec 27.
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Genome-wide CRISPR screens for Shiga toxins and ricin reveal Golgi proteins critical for glycosylation.全基因组 CRISPR 筛选志贺毒素和蓖麻毒素揭示了高尔基体蛋白在糖基化过程中的关键作用。
PLoS Biol. 2018 Nov 27;16(11):e2006951. doi: 10.1371/journal.pbio.2006951. eCollection 2018 Nov.
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High-resolution mapping and recognition of lipid domains using AFM with toxin-derivatized probes.利用毒素衍生探针的原子力显微镜进行高分辨率的脂筏定位和识别。
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Plasma membrane repair.质膜修复。
Curr Biol. 2018 Apr 23;28(8):R392-R397. doi: 10.1016/j.cub.2017.12.034.
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Triggered recruitment of ESCRT machinery promotes endolysosomal repair.ESCRT机制的触发募集促进内溶酶体修复。
Science. 2018 Apr 6;360(6384). doi: 10.1126/science.aar5078.
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Compartment-Specific Biosensors Reveal a Complementary Subcellular Distribution of Bioactive Furin and PC7.分区特异性生物传感器揭示了生物活性弗林和 PC7 的互补亚细胞分布。
Cell Rep. 2018 Feb 20;22(8):2176-2189. doi: 10.1016/j.celrep.2018.02.005.
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Glycosphingolipid metabolic reprogramming drives neural differentiation.糖脂代谢重编程驱动神经分化。
EMBO J. 2018 Apr 3;37(7). doi: 10.15252/embj.201797674. Epub 2017 Dec 27.
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