Department of Anatomy and Histology/Embryology, Faculty of Basic Medical Sciences, Kunming Medical University, 1168 West Chunrong Road, Kunming, 650500, P. R. China.
Department of Neurology, No.2 Affiliated Hospital, Kunming Medical University, 374 Dianmian Road, Kunming, 650101, P. R. China.
Adv Biol (Weinh). 2024 Jul;8(7):e2400123. doi: 10.1002/adbi.202400123. Epub 2024 Apr 29.
Scutellarin is an herbal agent which can exert anti-neuroinflammatory effects in activated microglia. However, it remains uncertain if it can inhibit microglia-mediated neuroinflammation by regulating miRNAs. This study sought to elucidate the upstream regulatory mechanisms by endogenous microRNAs and its target gene in activated microglia in lipopolysaccharide (LPS)-induced BV-2 microglia. Results show that scutellarin suppressed the expression of tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and inducible nitric oxide synthase (iNOS) significantly in LPS-stimulated BV-2 microglia. As with the results of miRNAs function classification in vitro, the expression levels of mir-7036a-5p are upregulated in LPS-activated BV-2 microglia, but are downregulated by scutellarin. Rescue experiments indicated that mir-7036a-5p is a pro-inflammatory factor in activated BV-2 microglia. mir-7036a-5p agomir promoted the expression of phosphorylated tau proteins (p-tau), protein kinase C gamma type (PRKCG), extracellular regulated protein kinases (ERK1/2), but the is reversed by mir-7036a-5p antagomir in vitro. It is shown here that mir-7036a-5p is involved in microglia-mediated inflammation in LPS-induced BV-2 microglia. More important is the novel finding that scutellarin mitigated microglia inflammation by down-regulating the mir-7036a-5p/MAPT/PRKCG/ERK signaling pathway.
野黄芩苷是一种草药成分,可在活化的小胶质细胞中发挥抗神经炎症作用。然而,它是否可以通过调节 microRNA 来抑制小胶质细胞介导的神经炎症仍然不确定。本研究旨在阐明内源性 microRNA 及其靶基因在脂多糖 (LPS) 诱导的 BV-2 小胶质细胞中活化的小胶质细胞中的上游调控机制。结果表明,野黄芩苷可显著抑制 LPS 刺激的 BV-2 小胶质细胞中肿瘤坏死因子-α (TNF-α)、白细胞介素-1β (IL-1β) 和诱导型一氧化氮合酶 (iNOS) 的表达。与体外 microRNA 功能分类的结果一致,在 LPS 激活的 BV-2 小胶质细胞中,mir-7036a-5p 的表达水平上调,但被野黄芩苷下调。拯救实验表明,mir-7036a-5p 是激活的 BV-2 小胶质细胞中的促炎因子。mir-7036a-5p agomir 促进磷酸化 tau 蛋白 (p-tau)、蛋白激酶 C 伽马型 (PRKCG) 和细胞外调节蛋白激酶 (ERK1/2) 的表达,但被 mir-7036a-5p antagomir 在体外逆转。研究表明,mir-7036a-5p 参与 LPS 诱导的 BV-2 小胶质细胞中的小胶质细胞介导的炎症。更重要的是,新发现野黄芩苷通过下调 mir-7036a-5p/MAPT/PRKCG/ERK 信号通路减轻小胶质细胞炎症。