Suppr超能文献

十字花科蔬菜中的植物抗毒素——莱菔硫烷通过脂肪细胞-巨噬细胞共培养体系中的 Nrf2-HO-1 信号通路抑制肥胖诱导的炎症反应。

Brassinin, a phytoalexin in cruciferous vegetables, suppresses obesity-induced inflammatory responses through the Nrf2-HO-1 signaling pathway in an adipocyte-macrophage co-culture system.

机构信息

Department of Public Health Sciences, Korea University, Seoul, Korea.

Department of Food Science and Technology, College of Natural Science, Seoul Women's University, Seoul, Korea.

出版信息

Phytother Res. 2019 May;33(5):1426-1437. doi: 10.1002/ptr.6333. Epub 2019 Mar 8.

Abstract

The aim of this study was to investigate the effect of brassinin (BR), a phytoalexin found in plants belonging to the Brassicaceae family, on the obesity-induced inflammatory response and its molecular mechanism in co-culture of 3T3-L1 adipocytes and RAW264.7 macrophages. BR effectively suppressed lipid accumulation by down-regulating the expression of adipogenic factors, which in turn, were regulated by early adipogenic factors such as CCAAT-enhancer-binding protein-β and Kruppel-like factor 2. Production of inflammatory cytokines and reactive oxygen species, induced by adipocyte-conditioned medium, was significantly decreased in BR-treated cells. This effect of BR was more prominent in contact co-culture of adipocytes and macrophages with a 90% and 34% reduction in IL-6 and MCP-1 levels, respectively. BR also restored adiponectin expression, which was significantly reduced by culturing adipocytes in macrophage-conditioned medium. In the transwell system, BR increased the protein levels of nuclear factor (erythroid-derived 2)-like 2 (Nrf2) and its target molecule, hemoxygenase-1 (HO-1), by 55%-93% and 45%-48%, respectively, and also increased Nrf2 translocation into the nucleus. However, knockdown of Nrf2 or HO-1 in RAW264.7 cells restored this BR-mediated inhibition of IL-6 and MCP-1 production. These results indicated that BR inhibited obesity-induced inflammation via the Nrf2-HO-1 pathway.

摘要

本研究旨在探讨植物中发现的植物抗毒素 brassinin (BR) 对 3T3-L1 脂肪细胞和 RAW264.7 巨噬细胞共培养物中肥胖引起的炎症反应及其分子机制的影响。BR 通过下调脂肪生成因子的表达有效抑制脂质积累,进而被早期脂肪生成因子如 CCAAT 增强子结合蛋白-β和 Kruppel 样因子 2 调节。由脂肪细胞条件培养基诱导的炎性细胞因子和活性氧的产生在 BR 处理的细胞中显著减少。BR 在脂肪细胞和巨噬细胞的接触共培养中作用更为显著,IL-6 和 MCP-1 水平分别降低了 90%和 34%。BR 还恢复了脂肪细胞在巨噬细胞条件培养基中培养时显著降低的脂联素表达。在 Transwell 系统中,BR 使核因子 (红细胞衍生 2)-样 2 (Nrf2) 及其靶分子血红素加氧酶-1 (HO-1) 的蛋白水平分别增加 55%-93%和 45%-48%,并增加 Nrf2 向核内易位。然而,在 RAW264.7 细胞中敲低 Nrf2 或 HO-1 恢复了 BR 介导的对 IL-6 和 MCP-1 产生的抑制作用。这些结果表明 BR 通过 Nrf2-HO-1 通路抑制肥胖引起的炎症。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验