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- 释放的细胞外囊泡对人单核细胞的生物学效应,诱导细胞毒性和炎症反应。

Biological Effect of -Released Extracellular Vesicles on Human Monocytic Cells, Induction of Cytotoxicity, and Inflammatory Response.

机构信息

Department of Microbiology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

HTLV-1/ATL Research Facility, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.

出版信息

Front Cell Infect Microbiol. 2021 Jul 19;11:711144. doi: 10.3389/fcimb.2021.711144. eCollection 2021.

DOI:10.3389/fcimb.2021.711144
PMID:34350134
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8326760/
Abstract

Most bacteria naturally release spherical lipid-bilayered extracellular vesicles (EVs) containing proteins, nucleic acids, and virulence-related molecules, thus contributing to diverse biological functions including transport of virulence factors. The group A streptococcus, (GAS), a major human pathogen, also releases EVs; however, it remains unclear how GAS EVs interact physiologically and pathologically with host cells, and what the differences are between invasive and non-invasive strains. The proteome profile in this study revealed that GAS EVs enclosed many virulence-related proteins such as streptolysin O and NAD-glycohydrolase, facilitating their pathogenicity, and invasive GAS EVs were more abundant than non-invasive counterparts. In terms of biological effects, invasive GAS EVs showed -dependent cytotoxic activity and the induction of cytokine expression, contributing to GAS pathogenicity directly. Although non-invasive GAS EVs did not show cytotoxic activity, they may be utilized as a means to prevent antibacterial mechanisms such as autophagy, leading to enhancement of their own survival in the intracellular environment after the infection. These results suggest that invasive and non-invasive GAS EVs play different roles in GAS infection strategy and pathogenicity. Our findings also indicate that EVs could be a key factor for GAS pathogenicity in GAS-host interactions.

摘要

大多数细菌自然释放含有蛋白质、核酸和与毒力相关分子的球形双层脂膜细胞外囊泡(EVs),从而有助于多种生物学功能,包括毒力因子的运输。化脓性链球菌(GAS)是一种主要的人类病原体,也会释放 EVs;然而,目前尚不清楚 GAS EVs 如何在生理和病理上与宿主细胞相互作用,以及侵袭性和非侵袭性菌株之间有何不同。本研究中的蛋白质组图谱显示,GAS EVs 包含许多与毒力相关的蛋白质,如链球菌溶血素 O 和 NAD-糖基水解酶,促进其致病性,侵袭性 GAS EVs 比非侵袭性菌株更为丰富。在生物学效应方面,侵袭性 GAS EVs 显示依赖于的细胞毒性活性和细胞因子表达的诱导,直接促进 GAS 的致病性。尽管非侵袭性 GAS EVs 没有显示出细胞毒性活性,但它们可能被用作一种手段来防止自噬等抗菌机制,从而增强其在感染后在细胞内环境中的存活能力。这些结果表明,侵袭性和非侵袭性 GAS EVs 在 GAS 感染策略和致病性中发挥不同的作用。我们的研究结果还表明,EVs 可能是 GAS 与宿主相互作用中 GAS 致病性的关键因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec57/8326760/3d15ece025a2/fcimb-11-711144-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec57/8326760/26a2c3b0d93c/fcimb-11-711144-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec57/8326760/5c7831db43b3/fcimb-11-711144-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec57/8326760/6356d33bfff8/fcimb-11-711144-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec57/8326760/95371799e233/fcimb-11-711144-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec57/8326760/868d6c54e892/fcimb-11-711144-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec57/8326760/3d15ece025a2/fcimb-11-711144-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec57/8326760/26a2c3b0d93c/fcimb-11-711144-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec57/8326760/5c7831db43b3/fcimb-11-711144-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec57/8326760/6356d33bfff8/fcimb-11-711144-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec57/8326760/95371799e233/fcimb-11-711144-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec57/8326760/868d6c54e892/fcimb-11-711144-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec57/8326760/3d15ece025a2/fcimb-11-711144-g006.jpg

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Cracking Open Bacterial Membrane Vesicles.
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