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膜囊泡在抑制自噬和细胞死亡中的新作用

A Novel Role of Membrane Vesicles in Inhibition of Autophagy and Cell Death.

作者信息

Vdovikova Svitlana, Luhr Morten, Szalai Paula, Nygård Skalman Lars, Francis Monika K, Lundmark Richard, Engedal Nikolai, Johansson Jörgen, Wai Sun N

机构信息

Department of Molecular Biology, Umeå UniversityUmeå, Sweden.

Laboratory for Molecular Infection Medicine Sweden, Umeå UniversityUmeå, Sweden.

出版信息

Front Cell Infect Microbiol. 2017 May 3;7:154. doi: 10.3389/fcimb.2017.00154. eCollection 2017.

Abstract

Bacterial membrane vesicle (MV) production has been mainly studied in Gram-negative species. In this study, we show that , a Gram-positive pathogen that causes the food-borne illness listeriosis, produces MVs both and . We found that a major virulence factor, the pore-forming hemolysin listeriolysin O (LLO), is tightly associated with the MVs, where it resides in an oxidized, inactive state. Previous studies have shown that LLO may induce cell death and autophagy. To monitor possible effects of LLO and MVs on autophagy, we performed assays for LC3 lipidation and LDH sequestration as well as analysis by confocal microscopy of HEK293 cells expressing GFP-LC3. The results revealed that MVs alone did not affect autophagy whereas they effectively abrogated autophagy induced by pure LLO or by another pore-forming toxin from , VCC. Moreover, MVs significantly decreased Torin1-stimulated macroautophagy. In addition, MVs protected against necrosis of HEK293 cells caused by the lytic action of LLO. We explored the mechanisms of LLO-induced autophagy and cell death and demonstrated that the protective effect of MVs involves an inhibition of LLO-induced pore formation resulting in inhibition of autophagy and the lytic action on eukaryotic cells. Further, we determined that these MVs help bacteria to survive inside eukaryotic cells (mouse embryonic fibroblasts). Taken together, these findings suggest that intracellular release of MVs from may represent a bacterial strategy to survive inside host cells, by its control of LLO activity and by avoidance of destruction from the autophagy system during infection.

摘要

细菌膜泡(MV)的产生主要在革兰氏阴性菌中得到研究。在本研究中,我们表明,一种导致食源性李斯特菌病的革兰氏阳性病原体,在[具体条件1]和[具体条件2]下均能产生MV。我们发现,一种主要的毒力因子,即形成孔道的溶血素李斯特菌溶素O(LLO),与MV紧密相关,它以氧化的、无活性的状态存在于MV中。先前的研究表明,LLO可能诱导细胞死亡和自噬。为了监测LLO和MV对自噬的可能影响,我们进行了LC3脂化和LDH隔离测定,以及对表达GFP-LC3的HEK293细胞进行共聚焦显微镜分析。结果显示,单独的MV不影响自噬,而它们有效地消除了由纯LLO或来自[细菌名称]的另一种形成孔道的毒素VCC诱导的自噬。此外,MV显著降低了Torin1刺激的巨自噬。另外,MV保护HEK293细胞免受LLO的裂解作用引起的坏死。我们探索了LLO诱导自噬和细胞死亡的机制,并证明MV的保护作用涉及抑制LLO诱导的孔形成,从而抑制自噬和对真核细胞的裂解作用。此外,我们确定这些MV有助于细菌在真核细胞(小鼠胚胎成纤维细胞)内存活。综上所述,这些发现表明,[细菌名称]的MV在细胞内释放可能代表一种细菌在宿主细胞内存活的策略,通过控制LLO活性以及在感染期间避免自噬系统的破坏。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f414/5413512/79f9ffd29aaa/fcimb-07-00154-g0001.jpg

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