NHC Key Laboratory of Prevention and Treatment of Central Asia High Incidence Diseases, The First Affiliated Hospital, Shihezi University School of Medicine, Shihezi, Xinjiang, China.
Key Laboratory of Xinjiang Endemic and Ethnic Diseases, Shihezi University School of Medicine, Shihezi, Xinjiang, China.
Parasit Vectors. 2023 Sep 9;16(1):321. doi: 10.1186/s13071-023-05948-1.
Echinococcus granulosus cyst fluid (EgCF) weakens macrophage inflammatory responses, thereby enabling the parasite to evade the immune system. However, the role of histone modification in this process remains to be explored.
The levels of IL-6, TNF-α, IL-10, H3K4me3, and KDM5B were detected using quantitative real-time PCR, ELISA, and Western blotting. The enrichment of H3K4me3 and KDM5B at the promoter of inflammatory factors was detected by chromatin immunoprecipitation.
Based on EgCF-stimulated macrophage models, we found that EgCF significantly inhibited mRNA expression and protein secretion of IL-6 and TNF-α and upregulated mRNA expression of IL-10 under the influence of TLR4. EgCF lowered the level of H3K4me3 and promoted the transcription and protein stability of histone demethylase KDM5B. Chromatin immunoprecipitation analysis revealed that EgCF suppressed the enrichment of H3K4me3 modification at the promoters of TNF-α and IL-6 and downregulated their expression in macrophages. Additionally, the inhibition of KDM5B activity by CPI-455 weakened the anti-inflammatory effect of EgCF.
Our findings demonstrate a novel mechanism through which EgCF promotes KDM5B expression and inhibits the enrichment of H3K4me3 at the promoters of inflammatory cytokines to suppress the inflammatory response.
细粒棘球蚴囊液(EgCF)可减弱巨噬细胞的炎症反应,从而使寄生虫逃避免疫系统。然而,组蛋白修饰在此过程中的作用仍有待探讨。
采用实时定量 PCR、ELISA 和 Western blot 检测 IL-6、TNF-α、IL-10、H3K4me3 和 KDM5B 的水平。通过染色质免疫沉淀检测炎症因子启动子处 H3K4me3 和 KDM5B 的富集情况。
基于 EgCF 刺激的巨噬细胞模型,我们发现 EgCF 可显著抑制 TLR4 影响下的 IL-6 和 TNF-α 的 mRNA 表达和蛋白分泌,并上调 IL-10 的 mRNA 表达。EgCF 降低了 H3K4me3 的水平,并促进了组蛋白去甲基化酶 KDM5B 的转录和蛋白稳定性。染色质免疫沉淀分析显示,EgCF 抑制了 TNF-α 和 IL-6 启动子处 H3K4me3 修饰的富集,并下调了它们在巨噬细胞中的表达。此外,CPI-455 抑制 KDM5B 活性可减弱 EgCF 的抗炎作用。
本研究结果表明,EgCF 通过促进 KDM5B 表达和抑制炎症细胞因子启动子处 H3K4me3 的富集来抑制炎症反应,从而为其发挥抗炎作用提供了一种新的机制。