IRF5公司
小胶质细胞
炎症
干扰素调节因子
免疫学
脂多糖
肿瘤坏死因子α
巨噬细胞
细胞因子
干扰素
医学
生物
免疫系统
先天免疫系统
体外
生物化学
摘要
Abstract Background Activated microglia plays a central role in neuro‐inflammation in central nervous system (CNS), which is involved in the progress of disease. Interferon regulatory factor 5 (IRF5) has been well established relating to inflammatory responses and is highly expressed in M1 macrophage in periphery, the role of which in the CNS remains elusive. Method Down‐regulation of IRF5 by siRNA in C57/BL6 mice and BV2 microglial cells was employed. Lipopolysaccharide (LPS) challenge activates the response of neuro‐inflammation, Pro‐inflammatory cytokines were evaluated by ELISA, western blot, and real‐time PCR. Result LPS induced the activation of microglia, which co‐localized with the significantly increase expression of IRF5. Down‐regulation of IRF5 significantly quenched the pro‐inflammatory responses. The levels of pro‐inflammatory cytokine TNF‐α, IL‐1βand IL‐6 were significantly up‐regulated at 4h after LPS treatment, which were reduced with the down‐regulation of IRF5. However, LPS did not up‐regulate the expression of IRF5 in BV2 microglial cells, indicating that LPS induced inflammation does not involve IRF5 signaling. Conclusion IRF5 plays an important role in the inflammatory responses in the CNS, which might serve as a therapeutic target for CNS inflammatory diseases. BV2 microglia is not an ideal cell line for the studies involves IRF5.
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