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牙龈卟啉单胞菌感染增强Th17反应,促进动脉粥样硬化的发展。

Porphyromonas gingivalis infection enhances Th17 responses for development of atherosclerosis.

作者信息

Cai Yu, Kobayashi Ryoki, Hashizume-Takizawa Tomomi, Kurita-Ochiai Tomoko

机构信息

Department of Microbiology and Immunology, Nihon University School of Dentistry at Matsudo, Sakaecho-nishi 2-870-1, Matsudo, Chiba 271-8587, Japan; Department of Periodontology, Peking University School and Hospital of Stomatology, 22 Zhongguancun Avenue South, Haidian District, Beijing 100081, PR China.

Department of Microbiology and Immunology, Nihon University School of Dentistry at Matsudo, Sakaecho-nishi 2-870-1, Matsudo, Chiba 271-8587, Japan.

出版信息

Arch Oral Biol. 2014 Nov;59(11):1183-91. doi: 10.1016/j.archoralbio.2014.07.012. Epub 2014 Jul 24.

Abstract

OBJECTIVES

Porphyromonas gingivalis has been shown to associate with the development of atherosclerosis. Recent studies indicate that IL-17-producing T helper 17 (Th17) cells have been correlated with the emergence of atherosclerosis. Therefore, we investigated whether the Th17 cell response and expression of Th17-related molecules, in contrast with Th1- and Treg cells, are enhanced by P. gingivalis-challenge in Apolipoprotein E knockout (ApoE KO) mice.

DESIGN

Five mice were intravenously injected with P. gingivalis three times a week for 3 weeks and killed at 15 weeks of age. The proximal aorta lesion area, flow cytometry analysis and IL-17, IL-10, IFN-γ, and IL-1β levels in splenic cultures, and expression of Th17-related molecules in spleen and hearts were examined.

RESULTS

P. gingivalis-challenge showed notable accumulation of atherosclerotic plaques by Oil Red O-staining in ApoE KO mice. Intracellular cytokine staining revealed that significantly elevated CD4(+) interleukin (IL)-17A(+) T cells and slightly increased CD4(+) Foxp3(+) T cells was recognized in spleen cells of P. gingivalis-challenged mice compared with those from non-infected mice. P. gingivalis-challenge significantly increased IL-17 and IL-1β production and RORγt expression in splenic cells. Furthermore, the expression of Th17-related genes such as IL-6, TGF-β, RORγt and STAT3 were elevated in splenic cells as well as heart tissue of P. gingivalis-challenged mice.

CONCLUSION

These results suggest that P. gingivalis infection may enhance pro-inflammatory Th17 cell responses in lesion areas and spleen, thereby accelerating atherosclerosis.

摘要

目的

牙龈卟啉单胞菌已被证明与动脉粥样硬化的发展有关。最近的研究表明,产生白细胞介素-17(IL-17)的辅助性T细胞17(Th17)与动脉粥样硬化的出现相关。因此,我们研究了与Th1细胞和调节性T细胞(Treg)相比,在载脂蛋白E基因敲除(ApoE KO)小鼠中,牙龈卟啉单胞菌攻击是否会增强Th17细胞反应以及Th17相关分子的表达。

设计

每周三次给五只小鼠静脉注射牙龈卟啉单胞菌,持续3周,并在15周龄时处死。检查近端主动脉病变面积、流式细胞术分析以及脾细胞培养物中IL-17、IL-10、干扰素-γ(IFN-γ)和IL-1β水平,以及脾脏和心脏中Th17相关分子的表达。

结果

通过油红O染色,在ApoE KO小鼠中,牙龈卟啉单胞菌攻击显示出动脉粥样硬化斑块的显著积累。细胞内细胞因子染色显示,与未感染小鼠相比,在牙龈卟啉单胞菌攻击的小鼠脾细胞中,CD4(+)白细胞介素(IL)-17A(+) T细胞显著升高,CD4(+) Foxp3(+) T细胞略有增加。牙龈卟啉单胞菌攻击显著增加了脾细胞中IL-17和IL-1β的产生以及维甲酸相关孤儿受体γt(RORγt)的表达。此外,在牙龈卟啉单胞菌攻击的小鼠的脾细胞以及心脏组织中,IL-6、转化生长因子-β(TGF-β)、RORγt和信号转导子和转录激活子3(STAT3)等Th17相关基因的表达也升高。

结论

这些结果表明,牙龈卟啉单胞菌感染可能会增强病变区域和脾脏中促炎性Th17细胞反应,从而加速动脉粥样硬化。

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