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二十二碳六烯酸通过GPR120介导的信号通路对RAW264.7细胞激活的免疫调节活性

Immunomodulatory Activity of Docosahexenoic Acid on RAW264.7 Cells Activation through GPR120-Mediated Signaling Pathway.

作者信息

Han Lirong, Yu Jun, Chen Yuanyuan, Cheng Dai, Wang Xu, Wang Chunling

机构信息

Key Laboratory of Food Nutrition and Safety, Ministry of Education, College of food Engineering and Biotechnology, Tianjin University of Science and Technology , No. 29, 13th Avenue, Tianjin Economy Technological Development Area, Tianjin 300457, People Republic of China.

出版信息

J Agric Food Chem. 2018 Jan 31;66(4):926-934. doi: 10.1021/acs.jafc.7b05894. Epub 2018 Jan 18.

Abstract

In this study, we elucidated the immunomodulatory activity of docosahexaenoic acid (DHA) on protein expression in RAW264.7 cells and its molecular mechanism. The results showed that the proliferation index of RAW264.7 cells at 48 h was about 173.03 ± 7.82% after the treatment of 2.4 μM DHA. DHA could activate RAW264.7 cells by the G-protein coupled cell membrane receptor GPR120-C-Raf- mitogen-activated protein kinases (MAPKs)-nuclear factor κB (NF-κB) p65 pathway. In addition, 2.4 μM of DHA could significantly increase (P < 0.01) the mRNA and protein expression of inducible nitric oxide synthase (iNOS), which is consistent with the result of the NO release. ELISA results revealed that DHA could enhance the protein expression of cytokines IL-1β, IL-6, IL-10, IL-12, TNF-α, IFN-γ, and TGF-β. These results indicated that the immunomodulatory mechanism of RAW264.7 cells by DHA was associated with the release of NO and cytokines by stimulating the GPR120, C-Raf, and MAPKs to the NF-κB p65 pathway.

摘要

在本研究中,我们阐明了二十二碳六烯酸(DHA)对RAW264.7细胞中蛋白质表达的免疫调节活性及其分子机制。结果显示,用2.4 μM DHA处理后,RAW264.7细胞在48小时的增殖指数约为173.03±7.82%。DHA可通过G蛋白偶联细胞膜受体GPR120-C-Raf-丝裂原活化蛋白激酶(MAPKs)-核因子κB(NF-κB)p65途径激活RAW264.7细胞。此外,2.4 μM的DHA可显著增加(P<0.01)诱导型一氧化氮合酶(iNOS)的mRNA和蛋白表达,这与NO释放的结果一致。ELISA结果显示,DHA可增强细胞因子IL-1β、IL-6、IL-10、IL-12、TNF-α、IFN-γ和TGF-β的蛋白表达。这些结果表明,DHA对RAW264.7细胞的免疫调节机制与通过刺激GPR120、C-Raf和MAPKs至NF-κB p65途径释放NO和细胞因子有关。

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