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链球菌细胞外膜囊泡被免疫细胞快速内吞,并改变其细胞因子释放。

Streptococcal Extracellular Membrane Vesicles Are Rapidly Internalized by Immune Cells and Alter Their Cytokine Release.

机构信息

Biogenic Nanotherapeutics Group, Helmholtz Institute for Pharmaceutical Research Saarland, Saarbrücken, Germany.

Department of Pharmacy, Saarland University, Saarbrücken, Germany.

出版信息

Front Immunol. 2020 Feb 14;11:80. doi: 10.3389/fimmu.2020.00080. eCollection 2020.

Abstract

Extracellular vesicles are membranous structures shed by almost every living cell. Bacterial gram-negative outer membrane vesicles (OMVs) and gram-positive membrane vesicles (MVs) play important roles in adaptation to the surrounding environment, cellular components' exchange, transfer of antigens and virulence factors, and infection propagation. is considered one of the priority pathogens, with a global health impact due to the increase in infection burden and growing antibiotic resistance. We isolated MVs produced from the reference strain (R6) and purified them via size exclusion chromatography (SEC) to remove soluble protein impurities. We characterized the isolated MVs by nanoparticle tracking analysis (NTA) and measured their particle size distribution and concentration. Isolated MVs showed a mean particle size range of 130-160 nm and a particle yield of around 10 particles per milliliter. Cryogenic transmission electron microscopy (cryo-TEM) images revealed a very heterogeneous nature of isolated MVs with a broad size range and various morphologies, arrangements, and contents. We incubated streptococcal MVs with several mammalian somatic cells, namely, human lung epithelial A549 and human keratinocytes HaCaT cell lines, and immune cells including differentiated macrophage-like dTHP-1 and murine dendritic DC2.4 cell lines. All cell lines displayed excellent viability profile and negligible cytotoxicity after 24-h incubation with MVs at concentrations reaching 10 MVs per cell (somatic cells) and 10 MVs per cell (immune cells). We evaluated the uptake of fluorescently labeled MVs into these four cell lines, using flow cytometry and confocal microscopy. Dendritic cells demonstrated prompt uptake after 30-min incubation, whereas other cell lines showed increasing uptake after 2-h incubation and almost complete colocalization/internalization of MVs after only 4-h incubation. We assessed the influence of streptococcal MVs on antigen-presenting cells, e.g., dendritic cells, using enzyme-linked immunosorbent assay (ELISA) and observed enhanced release of tumor necrosis factor (TNF)-α, a slight increase of interleukin (IL)-10 secretion, and no detectable effect on IL-12. Our study provides a better understanding of gram-positive streptococcal MVs and shows their potential to elicit a protective immune response. Therefore, they could offer an innovative avenue for safe and effective cell-free vaccination against pneumococcal infections.

摘要

细胞外囊泡是几乎所有活细胞分泌的膜状结构。革兰氏阴性细菌的外膜囊泡 (OMVs) 和革兰氏阳性膜囊泡 (MVs) 在适应周围环境、细胞成分交换、抗原和毒力因子转移以及感染传播方面发挥着重要作用。 被认为是优先病原体之一,由于感染负担增加和抗生素耐药性不断增强,对全球健康产生影响。我们从 参考株 (R6) 中分离出 MVs ,并通过分子筛层析 (SEC) 对其进行纯化,以去除可溶性蛋白杂质。我们通过纳米颗粒跟踪分析 (NTA) 对分离出的 MVs 进行了表征,并测量了它们的粒径分布和浓度。分离出的 MVs 的平均粒径范围为 130-160nm ,粒径产率约为每毫升 10 个颗粒。低温透射电子显微镜 (cryo-TEM) 图像显示,分离出的 MVs 具有非常异质的性质,具有广泛的粒径范围和各种形态、排列和内容。我们将链球菌 MVs 与几种哺乳动物体细胞(即人肺上皮 A549 和人角质形成细胞 HaCaT 细胞系)和免疫细胞(包括分化的巨噬细胞样 dTHP-1 和鼠树突状 DC2.4 细胞系)孵育。在用 MVs 孵育 24 小时后,所有细胞系均显示出良好的存活率,并且在浓度达到每细胞 10MVs(体细胞)和每细胞 10MVs(免疫细胞)时,细胞毒性可忽略不计。我们使用流式细胞术和共聚焦显微镜评估了荧光标记的 MVs 进入这四种细胞系的摄取情况。树突状细胞在孵育 30 分钟后迅速摄取,而其他细胞系在孵育 2 小时后摄取增加,仅孵育 4 小时后 MVs 几乎完全共定位/内化。我们评估了链球菌 MVs 对抗原呈递细胞(例如树突状细胞)的影响,例如使用酶联免疫吸附试验 (ELISA) 观察到肿瘤坏死因子 (TNF)-α 的释放增加,白细胞介素 (IL)-10 分泌略有增加,并且对 IL-12 没有可检测的影响。我们的研究更好地了解了革兰氏阳性链球菌 MVs ,并表明它们具有引发保护性免疫反应的潜力。因此,它们可能为安全有效的无细胞肺炎球菌感染疫苗提供新的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4540/7034238/4e35ab397ac1/fimmu-11-00080-g0001.jpg

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