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人树突状细胞在受到包封或未包封的同基因菌株刺激后的差异反应 。 (注:原文中“of”后面缺少具体内容)

Differential Response of Human Dendritic Cells upon Stimulation with Encapsulated or Non-Encapsulated Isogenic Strains of .

作者信息

Melgar-Rodríguez Samanta, Polanco Alan, Ríos-Muñoz Jearitza, García Michelle, Sierra-Cristancho Alfredo, González-Osuna Luis, Díaz-Zúñiga Jaime, Carvajal Paola, Vernal Rolando, Bravo Denisse

机构信息

Periodontal Biology Laboratory, Faculty of Dentistry, Universidad de Chile, Santiago 8380492, Chile.

Department of Conservative Dentistry, Faculty of Dentistry, Universidad de Chile, Santiago 8380492, Chile.

出版信息

Int J Mol Sci. 2024 Apr 20;25(8):4510. doi: 10.3390/ijms25084510.

Abstract

During periodontitis, the extracellular capsule of favors alveolar bone loss by inducing Th1 and Th17 patterns of lymphocyte response in the infected periodontium. Dendritic cells recognize bacterial antigens and present them to T lymphocytes, defining their activation and polarization. Thus, dendritic cells could be involved in the Th1 and Th17 response induced against the capsule. Herein, monocyte-derived dendritic cells were obtained from healthy individuals and then stimulated with different encapsulated strains of or two non-encapsulated isogenic mutants. Dendritic cell differentiation and maturation were analyzed by flow cytometry. The mRNA expression levels for distinct Th1-, Th17-, or T-regulatory-related cytokines and transcription factors, as well as TLR2 and TLR4, were assessed by qPCR. In addition, the production of IL-1β, IL-6, IL-23, and TNF-α was analyzed by ELISA. The encapsulated strains and non-encapsulated mutants of induced dendritic cell maturation to a similar extent; however, the pattern of dendritic cell response was different. In particular, the encapsulated strains of induced higher expression of IRF4 and NOTCH2 and production of IL-1β, IL-6, IL-23, and TNF-α compared with the non-encapsulated mutants, and thus, they showed an increased capacity to trigger Th1 and Th17-type responses in human dendritic cells.

摘要

在牙周炎期间,[具体细菌名称]的细胞外荚膜通过在受感染的牙周组织中诱导淋巴细胞反应的Th1和Th17模式,促进牙槽骨丧失。树突状细胞识别细菌抗原并将其呈递给T淋巴细胞,从而确定它们的激活和极化。因此,树突状细胞可能参与针对[具体细菌名称]荚膜诱导的Th1和Th17反应。在此,从健康个体中获得单核细胞衍生的树突状细胞,然后用不同的[具体细菌名称]荚膜菌株或两种无荚膜同基因突变体进行刺激。通过流式细胞术分析树突状细胞的分化和成熟。通过qPCR评估不同的Th1、Th17或T调节相关细胞因子和转录因子以及TLR2和TLR4的mRNA表达水平。此外,通过ELISA分析IL-1β、IL-6、IL-23和TNF-α的产生。[具体细菌名称]的荚膜菌株和无荚膜突变体在相似程度上诱导树突状细胞成熟;然而,树突状细胞反应模式不同。特别是,与无荚膜突变体相比,[具体细菌名称]的荚膜菌株诱导更高的IRF4和NOTCH2表达以及IL-1β、IL-6、IL-23和TNF-α的产生,因此,它们在人树突状细胞中显示出触发Th1和Th17型反应的能力增强。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b886/11049913/3dff35c19b20/ijms-25-04510-g001.jpg

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