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姜黄素通过调节小胶质细胞中 miR-199b-5p/IκB 激酶β(IKKβ)/核因子 kappa B(NF-κB)通路缓解脂多糖(LPS)激活的神经炎症。

Curcumin Alleviates Lipopolysaccharide (LPS)-Activated Neuroinflammation via Modulation of miR-199b-5p/IκB Kinase β (IKKβ)/Nuclear Factor Kappa B (NF-κB) Pathway in Microglia.

机构信息

Department of Physiology, School of Medicine of Yan'an University, Yan'an, Shaanxi, China (mainland).

Department of Videography, School of Medicine of Yan'an University, Yan'an, Shaanxi, China (mainland).

出版信息

Med Sci Monit. 2019 Dec 21;25:9801-9810. doi: 10.12659/MSM.918237.

Abstract

BACKGROUND Microglia reside in the spinal cord plays a key role in the onset, progression of post-spinal cord injury (SCI) neuroinflammation. Curcumin has been shown to exhibit diverse anti-inflammatory and anti-tumor activities. The aim of this study was to explore the effect of curcumin on the inflammatory response in lipopolysaccharide (LPS)-activated microglia and its mechanism. MATERIAL AND METHODS The expression levels of phosphorylated-p65 (p-p65), tumor necrosis factor (TNF)-alpha, interleukin (IL)-1ß, and IkappaB kinase ß (IKKß) were examined by western blot assay. MiR-199b-5p expression was detected by quantitative real-time polymerase chain reaction assay. The putative binding sites of miR-199b-5p in IKKß 3'UTR were predicted by bioinformatics, and direct interaction between miR-199b-5p and IKKß was verified by dual-luciferase reporter assay and RNA-immunoprecipitation assay. RESULTS Curcumin significantly suppressed inflammatory response induced by LPS by inactivation of nuclear factor kappa B (NF-kappaB) in microglial cells, as reflected by the decreased levels of p-p65, as well as the pro-inflammatory mediators, including inducible nitric oxide synthase (iNOS), TNF-alpha, and IL-1ß. Moreover, curcumin increased the level of miR-199b-5p and decreased IKKß expression in activated microglial cells. Knockdown of miR-199b-5p or overexpression of IKKß reversed the inhibitory effect of curcumin on inflammatory response and NF-kappaB activation. MiR-199b-5p directly targeted IKKß and suppressed its expression. Silencing of IKKß abolished miR-199b-5p-stimulated inflammatory cytokines production and NF-kappaB activation. CONCLUSIONS Curcumin attenuated neuroinflammation induced by LPS through regulating miR-199b-5p/IKKß/NF-kappaB axis in microglia.

摘要

背景

小胶质细胞存在于脊髓中,在脊髓损伤后(SCI)神经炎症的发病和进展中起着关键作用。姜黄素已显示出多种抗炎和抗肿瘤活性。本研究旨在探讨姜黄素对脂多糖(LPS)激活的小胶质细胞炎症反应的影响及其机制。

材料和方法

通过 Western blot 检测磷酸化 p65(p-p65)、肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β和 IKKβ的表达水平。通过实时定量聚合酶链反应检测 miR-199b-5p 的表达。通过生物信息学预测 miR-199b-5p 在 IKKβ 3'UTR 中的假定结合位点,并通过双荧光素酶报告基因检测和 RNA 免疫沉淀检测验证 miR-199b-5p 与 IKKβ 之间的直接相互作用。

结果

姜黄素通过抑制核因子 kappa B(NF-kappaB)在小胶质细胞中的活化,显著抑制 LPS 诱导的炎症反应,表现为 p-p65 水平以及诱导型一氧化氮合酶(iNOS)、TNF-α和 IL-1β等促炎介质水平降低。此外,姜黄素增加了激活的小胶质细胞中 miR-199b-5p 的水平并降低了 IKKβ 的表达。miR-199b-5p 敲低或 IKKβ 过表达逆转了姜黄素对炎症反应和 NF-kappaB 活化的抑制作用。miR-199b-5p 直接靶向 IKKβ 并抑制其表达。沉默 IKKβ 消除了 miR-199b-5p 刺激的炎症细胞因子产生和 NF-kappaB 活化。

结论

姜黄素通过调节小胶质细胞中 miR-199b-5p/IKKβ/NF-kappaB 轴减轻 LPS 诱导的神经炎症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95d7/6937907/eb96b7a7ff60/medscimonit-25-9801-g001.jpg

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