首页> 外文期刊>Carbohydrate Polymers: Scientific and Technological Aspects of Industrially Important Polysaccharides >Chitosan oligosaccharides inhibit LPS-induced over-expression of IL-6 and TNF-α in RAW264.7 macrophage cells through blockade of mitogen-activated protein kinase (MAPK) and PI3K/Akt signaling pathways
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Chitosan oligosaccharides inhibit LPS-induced over-expression of IL-6 and TNF-α in RAW264.7 macrophage cells through blockade of mitogen-activated protein kinase (MAPK) and PI3K/Akt signaling pathways

机译:壳聚糖寡糖通过阻断有丝分裂原激活的蛋白激酶(MAPK)和PI3K / Akt信号通路来抑制LPS诱导的RAW264.7巨噬细胞中IL-6和TNF-α的过表达

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摘要

Chitosan oligomers show various biological activities. However, its molecular mechanisms remain unknown in LPS-stimulated macrophages. Here, we explored the inhibitive effects of chitosan oligomers on LPS-induced IL-6/TNF-α production in macrophages. The results indicated chitosan oligomers pre-treatment effectively inhibited LPS-induced over-expression of both inflammatory cytokines. Signal transduction studies show chitosan oligomers may repress not only the phosphorylation of p38, ERK1 /2, JNK, phosphatidylinositol 3-kinase (PI3K) and Akt, but also the activation of nuclear factor-KB (NF-kB) and activator protein-1 (AP-1). Furthermore/both the activation of NF-kB/AP-1 and the subsequent IL-6/TNF-α over-expression in LPS-induced macrophages are inhibited by specific p38 inhibitor (SB203580), ERK1/2 inhibitor (PD98059), JNK inhibitor (SP600125) and PI3K inhibitor (LY294002). In conclusion, our investigation suggests chitosan oligomers inhibited the elevated expression of IL-6/TNF-α in LPS-induced macrophages, regulated by MAPKs and P13K/Akt pathways dependent on NF-kB/AP-1 activation.
机译:壳聚糖低聚物显示出各种生物活性。但是,其分子机制在LPS刺激的巨噬细胞中仍然未知。在这里,我们探讨了壳聚糖寡聚体对巨噬细胞中LPS诱导的IL-6 /TNF-α产生的抑制作用。结果表明,壳聚糖低聚物预处理可有效抑制LPS诱导的两种炎性细胞因子的过表达。信号转导研究表明,壳聚糖低聚物不仅可以抑制p38,ERK1 / 2,JNK,磷脂酰肌醇3-激酶(PI3K)和Akt的磷酸化,而且还可以抑制核因子KB(NF-kB)和激活蛋白1的活化。 (AP-1)。此外,特异性p38抑制剂(SB203580),ERK1 / 2抑制剂(PD98059),JNK抑制了LPS诱导的巨噬细胞中NF-kB / AP-1的激活和随后的IL-6 /TNF-α的过度表达。抑制剂(SP600125)和PI3K抑制剂(LY294002)。总之,我们的研究表明壳聚糖低聚物抑制了LPS诱导的巨噬细胞中IL-6 /TNF-α的表达升高,并受依赖于NF-kB / AP-1激活的MAPK和P13K / Akt途径调控。

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