首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Sophora subprosrate polysaccharide suppress the inflammatory reaction of RAW264.7 cells infected with PCV2 via regulation NF-kappa B/MAPKs/c-Jun signal pathway and histone acetylation modification
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Sophora subprosrate polysaccharide suppress the inflammatory reaction of RAW264.7 cells infected with PCV2 via regulation NF-kappa B/MAPKs/c-Jun signal pathway and histone acetylation modification

机译:Sophora脱喹啉多糖抑制了通过调节NF-Kappa B / MAPK / C-Jun信号途径和组蛋白乙酰化改性感染PCV2的Raw264.7细胞的炎症反应

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The purpose of this study was to investigate the regulation of Sophora subprosrate polysaccharide (SSP) on inflammatory response and histone acetylation modification of RAW264.7 cells (mouse mononuclear macrophage cell line) infected with porcine circovirus type 2 (PCV2). We further explored the role of inflammatory response and histone acetylation modification on the basis of the original study. The results showed that SSP decreased the secretion levels of TNF-alpha and IL-6 and the intracellular iNOS, COX-2 enzyme activities and their mRNA expression levels in PCV2 infected RAW264.7 cells, but increased the level of IL-10 secretion and its mRNA expression. SSP inhibited the phosphorylation levels of proteins of p65, ERK1/2, p38 and c-Jun in RAW264.7 cells infected with PCV2. The activities of HAT and HDAC enzymes and the mRNA expression levels of HAT1 and HDAC1 were increased when the PCV2-infected RAW264.7 cells were treated by SSP. Meanwhile, the expression of acetylation modification of histones both H3 and H4 was obviously inhibited. In conclusion, SSP may reduce the acetylation levels of both H3 and H4 and activate NF-kappa B/MAPKs/c-Jun signaling pathway by increasing the activity of HADC enzyme and the expression of HDAC mRNA, further inhibiting inflammatory response by regulating the gene expression levels of inflammatory factors. The findings indicated that the molecular mechanism of how traditional Chinese medicine polysaccharide regulates inflammatory signal pathways and inflammatory factors by regulating histone acetylation. (C) 2020 Elsevier B.V. All rights reserved.
机译:本研究的目的是探讨患有猪循环系统型2(PCV2)感染的Raw264.7细胞(小鼠单核巨噬细胞系)对炎症反应和组蛋白乙酰化改性的Sophora脱喹啉多糖(SSP)的调节。我们进一步探讨了炎症反应和组蛋白乙酰化修饰在原始研究的基础上的作用。结果表明,SSP降低了TNF-α和IL-6的分泌水平和细胞内InOS,Cox-2酶活性及其PCV2感染的Raw264.7细胞的MRNA表达水平,但增加了IL-10分泌水平和它的mRNA表达。 SSP抑制P65,ERK1 / 2,P38和C-Jun的磷酸化水平,在Raw264.7细胞中感染PCV2。当SSP处理PCV2感染的Raw264.7细胞时,帽子和HDAC酶的活性和HAT1和HDAC1的mRNA表达水平增加。同时,明显抑制了组蛋白的乙酰化改性的表达。总之,SSP可以通过增加HADC酶的活性和HDAC mRNA的表达,通过调节基因来降低H3和H4的乙酰化水平,并通过增加HDAC mRNA的表达,通过调节基因来进一步抑制炎症反应来激活NF-Kappa B / MAPK / C-Jun信号传导途径炎症因素的表达水平。结果表明,通过调节组蛋白乙酰化,中药多糖如何调节炎症信号途径和炎症因子的分子机制。 (c)2020 Elsevier B.v.保留所有权利。

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