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源自[具体内容未给出]的外膜囊泡通过诱导内皮细胞白细胞介素-8来调节中性粒细胞迁移。

Outer Membrane Vesicles Derived From Regulate Neutrophil Migration by Induction of Endothelial IL-8.

作者信息

Lee Jaewook, Yoon Yae Jin, Kim Ji Hyun, Dinh Nhung Thi Hong, Go Gyeongyun, Tae Sookil, Park Kyong-Su, Park Hyun Taek, Lee Changjin, Roh Tae-Young, Di Vizio Dolores, Gho Yong Song

机构信息

Department of Life Sciences, Pohang University of Science and Technology, Pohang, South Korea.

Division of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology, Pohang, South Korea.

出版信息

Front Microbiol. 2018 Oct 11;9:2268. doi: 10.3389/fmicb.2018.02268. eCollection 2018.

DOI:10.3389/fmicb.2018.02268
PMID:30369908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6194319/
Abstract

Outer membrane vesicles (OMVs) are spherical, proteolipid nanostructures that are constitutively released by Gram-negative bacteria including . Although it has been shown that administration of OMVs stimulates a strong pulmonary inflammatory response with infiltration of neutrophils into the lungs , the mechanism of OMV-mediated neutrophil recruitment is poorly characterized. In this study, we observed significant infiltration of neutrophils into the mouse lung tissues , with increased expression of the neutrophil chemoattractant CXCL1, a murine functional homolog of human IL-8, on intraperitoneal administration of OMVs. In addition, OMVs and CD31-positive endothelial cells colocalized in the mouse lungs. Moreover, results showed that OMVs significantly increased IL-8 release from human microvascular endothelial cells and toll-like receptor (TLR)4 was found to be the main component for recognizing OMVs among human endothelial cell-associated TLRs. Furthermore, the transmigration of neutrophils was suppressed in the lung tissues obtained from TLR4 knockout mice treated with OMVs. Taken together, our data demonstrated that OMVs potently recruit neutrophils into the lung via the release of IL-8/CXCL1 from endothelial cells in TLR4- and NF-κB-dependent manners.

摘要

外膜囊泡(OMVs)是球形的蛋白脂质纳米结构,由革兰氏阴性菌组成性释放,包括……。尽管已表明给予OMVs会刺激强烈的肺部炎症反应,导致中性粒细胞浸润到肺部,但OMV介导的中性粒细胞募集机制仍不清楚。在本研究中,我们观察到在腹腔注射OMVs后,小鼠肺组织中有大量中性粒细胞浸润,中性粒细胞趋化因子CXCL1(人IL-8的小鼠功能同源物)的表达增加。此外,OMVs与CD31阳性内皮细胞在小鼠肺中共定位。而且,结果表明OMVs显著增加人微血管内皮细胞释放IL-8,并且在人内皮细胞相关的Toll样受体(TLR)中,TLR4被发现是识别OMVs的主要成分。此外,在用OMVs处理的TLR4基因敲除小鼠的肺组织中,中性粒细胞的迁移受到抑制。综上所述,我们的数据表明OMVs通过以TLR4和NF-κB依赖的方式从内皮细胞释放IL-8/CXCL1,有效地将中性粒细胞募集到肺中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e9/6194319/0f15848603f4/fmicb-09-02268-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e9/6194319/36d28d609e09/fmicb-09-02268-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e9/6194319/9f67352b71c7/fmicb-09-02268-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e9/6194319/8fef29c9f4ff/fmicb-09-02268-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e9/6194319/2a2bf8c5c7be/fmicb-09-02268-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e9/6194319/0f15848603f4/fmicb-09-02268-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e9/6194319/36d28d609e09/fmicb-09-02268-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e9/6194319/9f67352b71c7/fmicb-09-02268-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e9/6194319/8fef29c9f4ff/fmicb-09-02268-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e9/6194319/2a2bf8c5c7be/fmicb-09-02268-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e9/6194319/0f15848603f4/fmicb-09-02268-g005.jpg

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