首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Activation of macrophages by polysaccharide isolated from Paecilomyces cicadae through toll-like receptor 4
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Activation of macrophages by polysaccharide isolated from Paecilomyces cicadae through toll-like receptor 4

机译:通过收费样受体4从蝉拟青霉分离的多糖激活巨噬细胞

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摘要

Paecilomyces cicadae have been reported to have immunomodulatory properties. In this study, we investigated the effect of polysaccharide (PCP) isolated from P. cicadae on the macrophages. PCP increased the production of nitric oxide (NO) and the gene expression of IL-1β, IL-6, and TNF-α in RAW 264.7 cells. To investigate the membrane receptor, we examined the effect of PCP on primary macrophages isolated from wild type C3H/HeN and C3H/HeJ mice having mutant-TLR4. PCP induced NO production and cytokine gene expression in macrophages from C3H/HeN, but not from tlr4-mutated C3H/HeJ mice, which suggests that TLR4 is the membrane receptor for PCP. PCP induced the phosphorylation of ERK, JNK, and p38, and the nuclear translocation of NF-κB p50/p65, which are the main signaling molecules downstream from TLR4. Among them, p38 and NF-κB signaling played a crucial role in PCP-induced NO production by macrophages. These results indicate that PCP activates macrophages through the TLR4 signaling pathway.
机译:蝉拟拟青霉具有免疫调节特性。在这项研究中,我们调查了蝉蝉多糖(PCP)分离对巨噬细胞的影响。 PCP可增加RAW 264.7细胞中一氧化氮(NO)的产生以及IL-1β,IL-6和TNF-α的基因表达。为了研究膜受体,我们检查了PCP对从具有突变型TLR4的野生型C3H / HeN和C3H / HeJ小鼠分离的初级巨噬细胞的作用。 PCP在C3H / HeN的巨噬细胞中诱导NO产生和细胞因子基因表达,但在tlr4突变的C3H / HeJ小鼠中却没有,这表明TLR4是PCP的膜受体。 PCP诱导ERK,JNK和p38的磷酸化,以及NF-κBp50 / p65的核易位,这是TLR4下游的主要信号分子。其中,p38和NF-κB信号传导在PCP诱导巨噬细胞产生NO中起关键作用。这些结果表明PCP通过TLR4信号通路激活巨噬细胞。

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