Suppr超能文献

人类白细胞在接触牙龈卟啉单胞菌脂多糖后的免疫反应。

Immunological response of human leucocytes after exposure to lipopolysaccharides from Porphyromonas gingivalis.

机构信息

Department of Oral Microbiology and Immunology, University of Gothenburg, The Sahlgrenska Academy, Institute of Odontology, Gothenburg, Sweden.

出版信息

Clin Exp Dent Res. 2021 Aug;7(4):531-538. doi: 10.1002/cre2.388. Epub 2020 Dec 29.

Abstract

UNLABELLED

Porphyromonas gingivalis (P. gingivalis) is a gram-negative bacterium and an important etiologic agent of periodontitis. P. gingivalis releases outer membrane vesicles containing lipopolysaccharides (LPS), which can penetrate periodontal tissues. Once in the periodontal tissues and in contact with immune cells, it may participate in the destructive innate host response associated with the disease. The exact mechanism of P. gingivalis LPS in the disease process is not clear, but it is known to affect a variety of immune responses.

OBJECTIVES

To investigate how LPS from P. gingivalis affect neutrophil extracellular trap (NET) formation, cell death and production of cytokines from human neutrophils and peripheral mononuclear blood mononuclear cells (PBMCs).

MATERIALS AND METHODS

Isolated neutrophils and PBMCs were cultured with LPS from P. gingivalis or Escherichia coli (E. coli) (control). The NET formation was measured using Sytox green stain. Cell death of neutrophils and PBMCs was analyzed using flow cytometry or Sytox green stain. Cytokine production was measured using enzyme-linked immunosorbent assay (ELISA) kit or Bio-Plex assay.

RESULTS

Exposure to LPS from P. gingivalis and E. coli caused significantly lower cell death in neutrophils. NETs were formed after exposure to the two different LPS. In PBMCs, exposure to P. gingivalis and E. coli LPS caused increased levels of IL-1β and IL-6 compared to unstimulated controls. Increased cell death in PBMCs after exposure to LPS from E. coli in comparison to LPS from P. gingivalis and unstimulated controls was also observed.

CONCLUSIONS

LPS from P. gingivalis has the ability to affect both human neutrophils and PBMCs with regard to cytokine production, cell death and production of NETs. LPS from P. gingivalis could be involved in the pathogenesis of periodontitis, and our results may contribute information regarding possible markers for diagnosis and targets for treatment of periodontal disease.

摘要

未加标签

牙龈卟啉单胞菌(P. gingivalis)是一种革兰氏阴性菌,也是牙周炎的重要病因。牙龈卟啉单胞菌释放含有脂多糖(LPS)的外膜囊泡,这些囊泡可以穿透牙周组织。一旦进入牙周组织并与免疫细胞接触,它可能会参与与疾病相关的破坏性固有宿主反应。牙龈卟啉单胞菌 LPS 在疾病过程中的确切机制尚不清楚,但已知它会影响多种免疫反应。

目的

研究牙龈卟啉单胞菌 LPS 如何影响人中性粒细胞的细胞外陷阱(NET)形成、细胞死亡和细胞因子的产生,以及外周血单核细胞(PBMCs)。

材料和方法

用牙龈卟啉单胞菌或大肠杆菌(E. coli)(对照)的 LPS 培养分离的中性粒细胞和 PBMCs。使用 Sytox green 染色测量 NET 形成。使用流式细胞术或 Sytox green 染色分析中性粒细胞和 PBMCs 的细胞死亡。使用酶联免疫吸附测定(ELISA)试剂盒或 Bio-Plex 测定法测量细胞因子的产生。

结果

暴露于牙龈卟啉单胞菌和大肠杆菌 LPS 会导致中性粒细胞的细胞死亡明显降低。两种不同 LPS 暴露后均形成 NET。在 PBMCs 中,与未刺激对照相比,暴露于牙龈卟啉单胞菌和大肠杆菌 LPS 会导致 IL-1β 和 IL-6 水平升高。与牙龈卟啉单胞菌 LPS 和未刺激对照相比,暴露于大肠杆菌 LPS 后 PBMCs 的细胞死亡也增加。

结论

牙龈卟啉单胞菌 LPS 具有影响人中性粒细胞和 PBMCs 细胞因子产生、细胞死亡和 NET 形成的能力。牙龈卟啉单胞菌 LPS 可能参与牙周炎的发病机制,我们的结果可能为牙周病的诊断提供可能的标志物和治疗靶点提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5419/8404501/20355ccd973e/CRE2-7-531-g005.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验