TREM2表达促进日本血吸虫感染小鼠肝脏和腹腔M2巨噬细胞极化

IF 5.3 2区 医学 Q1 Biochemistry, Genetics and Molecular Biology
Dandan Zhu, Min Huang, Pei Shen, Bei Zhang, Guo Chen, Jinling Chen, Lian Duan, Yinong Duan
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引用次数: 0

摘要

血吸虫病是一种损害肝脏的热带寄生虫病,对人类健康构成严重威胁。在血吸虫病中,巨噬细胞通过从M1到M2的极化,在肝脏肉芽肿和纤维化的发展中起着关键作用。因此,调节巨噬细胞极化对于控制本病期间发生的病理变化具有重要意义。巨噬细胞、树突状细胞等免疫细胞表面表达的髓样细胞2触发受体(TREM2)已被证明在抑制炎症反应和调节M2巨噬细胞极化中发挥作用,但其在血吸虫病巨噬细胞极化中的作用尚未被研究。在本研究中,我们证实了日本血吸虫感染小鼠的肝脏和腹腔巨噬细胞中TREM2表达上调。此外,TREM2的表达趋势与日本血吸虫感染小鼠肝组织中M2巨噬细胞极化相关分子的表达相关。使用Trem2−/−小鼠,我们还发现Trem2缺失抑制了肝脏组织中Arg1和Ym1的表达。Trem2缺失也增加了感染小鼠腹膜巨噬细胞中F4/80 + CD86+细胞的数量。综上所述,我们的研究提示TREM2可能参与血吸虫病期间M2巨噬细胞的极化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

TREM2 expression promotes liver and peritoneal M2 macrophage polarization in mice infected with Schistosoma japonicum

TREM2 expression promotes liver and peritoneal M2 macrophage polarization in mice infected with Schistosoma japonicum

Schistosomiasis is a tropical parasitic disease that damages the liver and poses a serious threat to human health. Macrophages play a key role in the development of liver granulomas and fibrosis by undergoing polarization from M1 to M2 type during schistosomiasis. Therefore, regulating macrophage polarization is important for controlling pathological changes that occur during this disease. Triggering receptor expressed on myeloid cells 2 (TREM2) expressed on the surface of macrophages, dendritic cells and other immune cells has been shown to play a role in inhibiting inflammatory responses and regulating M2 macrophage polarization, however its role in macrophage polarization in schistosomiasis has not been investigated. In this study, we confirmed that TREM2 expression was upregulated in the livers and peritoneal macrophages of mice infected with Schistosoma japonicum. Moreover, the TREM2 expression trend correlated with the expression of M2 macrophage polarization-related molecules in the liver tissues of S. japonicum-infected mice. Using Trem2−/− mice, we also showed that Trem2 deletion inhibited Arg1 and Ym1 expression in liver tissues. Trem2 deletion also increased the number of F4/80 + CD86+ cells in peritoneal macrophages of infected mice. In summary, our study suggests that TREM2 may be involved in M2 macrophage polarization during schistosomiasis.

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来源期刊
CiteScore
10.00
自引率
1.90%
发文量
496
审稿时长
28 weeks
期刊介绍: Bridging physiology and cellular medicine, and molecular biology and molecular therapeutics, Journal of Cellular and Molecular Medicine publishes basic research that furthers our understanding of the cellular and molecular mechanisms of disease and translational studies that convert this knowledge into therapeutic approaches.
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