Kong Delong, Guo Hongfei, Lu Zhongkui, Cui Jie
Jiangsu Key Laboratory of Immunity and Metabolism, Laboratory of Infection and Immunity, Department of Pathogenic Biology and Immunology, Xuzhou Medical University, Xuzhou, China.
Key Laboratory of Pathogen Biology of Jiangsu Province, Department of Pathogen Biology, Nanjing Medical University, Nanjing, China.
Front Vet Sci. 2020 Feb 12;6:517. doi: 10.3389/fvets.2019.00517. eCollection 2019.
Praziquantel (PZQ), a traditional helminthicide drug, has been shown to exert an anti-inflammatory effect on splenomegaly induced by schistosomiasis via regulating macrophage polarization. Meanwhile, miR-21 has been demonstrated to control macrophage polarization. However, the role of miR-21 in the regulation of macrophage polarization by PZQ in schistosomiasis is still unclear. In the present study, we found that M1-type macrophages were the predominant splenic macrophages in chronic schistosomiasis and that NLRP3 inflammasome-related molecules were upregulated. PZQ inhibited NLRP3 inflammasome in M1 macrophages and reduced the expression of miR-21. Furthermore, using the methods of quantitative real-time PCR and transfection, the downregulation of NLRP3/IL-1β by PZQ in M1 macrophages were reversed by miR-21 overexpression. These results indicated that miR-21 was involved in the inhibiting effect of PZQ on activation of NLRP3 inflammasome. Moreover, miR-21 might target Smad7 to mediate the anti-inflammatory effect of PZQ in polarized macrophages. This study provides an in-depth mechanism of PZQ in the treatment of schistosomiasis.
吡喹酮(PZQ)是一种传统的驱虫药物,已被证明可通过调节巨噬细胞极化对血吸虫病诱导的脾肿大发挥抗炎作用。同时,miR-21已被证明可控制巨噬细胞极化。然而,miR-21在血吸虫病中PZQ调节巨噬细胞极化的作用仍不清楚。在本研究中,我们发现M1型巨噬细胞是慢性血吸虫病中主要的脾巨噬细胞,且NLRP3炎性小体相关分子上调。PZQ抑制M1巨噬细胞中的NLRP3炎性小体并降低miR-21的表达。此外,使用定量实时PCR和转染方法,miR-21过表达逆转了PZQ在M1巨噬细胞中对NLRP3/IL-1β的下调作用。这些结果表明,miR-21参与了PZQ对NLRP3炎性小体激活的抑制作用。此外,miR-21可能靶向Smad7来介导PZQ在极化巨噬细胞中的抗炎作用。本研究为PZQ治疗血吸虫病提供了深入的机制。