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在小鼠巨噬细胞RAW 264.7中,的肽聚糖相关脂蛋白通过Toll样受体2(TLR2)诱导细胞凋亡和促炎细胞因子的产生。

Peptidoglycan-associated lipoprotein of induces apoptosis and production of proinflammatory cytokines via TLR2 in murine macrophages RAW 264.7 .

作者信息

Ihalin Riikka, Eneslätt Kjell, Asikainen Sirkka

机构信息

Department of Odontology, Oral Microbiology, Umeå University, Umeå, Sweden.

Department of Biochemistry, University of Turku, Turku, Finland.

出版信息

J Oral Microbiol. 2018 Mar 6;10(1):1442079. doi: 10.1080/20002297.2018.1442079. eCollection 2018.

Abstract

Peptidoglycan-associated lipoprotein (PAL) is a conserved pro-inflammatory outer membrane lipoprotein in Gram-negative bacteria. Compared to systemic pathogens, little is known about the virulence properties of PAL in (AaPAL). The aims of this study were to investigate the cytolethality of AaPAL and its ability to induce pro-inflammatory cytokine production in macrophages. Mouse macrophages were stimulated with AaPAL, and the production of IL-1β, IL-6, TNF-α, and MCP-1 was measured after 6, 24, and 48 h. To investigate which receptor AaPAL employs for its interaction with macrophages, anti-toll-like receptor (TLR)2 and anti-TLR4 antibodies were used to block respective TLRs on macrophages. Metabolic activity and apoptosis of the macrophages were investigated after stimulation with AaPAL. AaPAL induced the production of MCP-1, TNF-α, IL-6, and IL-1β from mouse macrophages in order of decreasing abundance. The pre-treatment of macrophages with an anti-TLR2 antibody significantly diminished cytokine production. Under AaPAL stimulation, the metabolic activity of macrophages decreased in a dose- and time-dependent manner. Furthermore, AaPAL induced apoptosis in 56% of macrophages after 48 h of incubation. Our data suggest that AaPAL can kill macrophages by apoptosis. The results also emphasize the role of AaPAL as a potent pro-inflammatory agent in -associated infections.

摘要

肽聚糖相关脂蛋白(PAL)是革兰氏阴性菌中一种保守的促炎外膜脂蛋白。与全身性病原体相比,关于牙龈卟啉单胞菌脂蛋白(AaPAL)的毒力特性知之甚少。本研究的目的是调查AaPAL的细胞致死率及其在巨噬细胞中诱导促炎细胞因子产生的能力。用AaPAL刺激小鼠巨噬细胞,并在6、24和48小时后测量白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)和单核细胞趋化蛋白-1(MCP-1)的产生。为了研究AaPAL与巨噬细胞相互作用所利用的受体,使用抗Toll样受体(TLR)2和抗TLR4抗体来阻断巨噬细胞上各自的TLR。在用AaPAL刺激后,研究巨噬细胞的代谢活性和凋亡情况。AaPAL以丰度递减的顺序诱导小鼠巨噬细胞产生MCP-1、TNF-α、IL-6和IL-1β。用抗TLR2抗体预处理巨噬细胞可显著减少细胞因子的产生。在AaPAL刺激下,巨噬细胞的代谢活性呈剂量和时间依赖性降低。此外,孵育48小时后,AaPAL诱导56%的巨噬细胞凋亡。我们的数据表明AaPAL可通过凋亡杀死巨噬细胞。结果还强调了AaPAL在相关感染中作为一种强效促炎剂的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f64/5907638/e7c7aaadf2c8/ZJOM_A_1442079_F0001_B.jpg

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