首页> 外文期刊>Biological & pharmaceutical bulletin >Proteoglycan Isolated from Phellinus linteus Induces Toll-Like Receptors 2- and 4-Mediated Maturation of Murine Dendritic Cells via Activation of ERK, p38, and NF-kappaB.
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Proteoglycan Isolated from Phellinus linteus Induces Toll-Like Receptors 2- and 4-Mediated Maturation of Murine Dendritic Cells via Activation of ERK, p38, and NF-kappaB.

机译:从桑黄分离的蛋白聚糖通过激活ERK,p38和NF-κB诱导Toll样受体2和4介导的小鼠树突状细胞成熟。

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Mushroom polysaccharides are increasingly being utilized to treat a wide variety of diseases. Phellinus linteus proteoglycan (PL) has been reported to have anti-tumor and immunomodulatory properties. However, the cellular and molecular mechanism underlying its therapeutic effect is poorly understood. In this study, we investigated whether PL induces the phenotypic and functional maturation of murine bone marrow-derived dendritic cells (DC) and the possibility that Toll-like receptors (TLRs), which are known to be involved in immune-related responses, may be the receptor(s) of PL. The expression of surface molecules, including major histocompatibility complex (MHC) class II and CD86, increased on DC that were stimulated in a dose-dependent manner with PL, in comparison with unstimulated DC. Furthermore, PL increases the production of IL-12 by DC, as well as the IL-2 secretion and proliferation of allogeneic T cells. In addition, the activities of PL on DC were significantly reduced by treating the cellswith anti-TLR2 or anti-TLR4 antibody (Ab) prior to PL, suggesting that both of them are possible receptors of PL. Also, maturation of DC by PL was able to directly activate mitogen-activated protein kinases (MAPKs), such as ERK1/2 and p38, and the nuclear transcription factor NF-kappaB p65. Also, the pretreatment of DC with inhibitors of NF-kappaB p65, and ERK and p38 MAPK signal pathways inhibited PL-induced up-regulation of surface molecules, such as MHC class II and CD86, and IL-12 production. Our results demonstrated that PL stimulation could induce the phenotypic and functional maturation of DC via TLR2 and/or TLR4 mediated-NF-kappaB, ERK and p38 MAPK signal pathways.
机译:蘑菇多糖被越来越多地用于治疗多种疾病。桑黄蛋白聚糖(PL)据报道具有抗肿瘤和免疫调节特性。然而,对其治疗作用基础的细胞和分子机制了解甚少。在这项研究中,我们调查了PL是否会诱导鼠骨髓源性树突状细胞(DC)的表型和功能成熟,以及已知Toll样受体(TLR)参与免疫相关反应的可能性,是PL的受体。与未刺激的DC相比,用PL以剂量依赖性方式刺激的DC上的表面分子(包括主要的组织相容性复合物(MHC)II类和CD86)的表达增加。此外,PL增加了DC分泌IL-12的产量,以及同种异体T细胞的IL-2分泌和增殖。另外,通过在PL之前用抗TLR2或抗TLR4抗体(Ab)处理细胞,PL对DC的活性显着降低,表明它们都是PL的可能受体。同样,通过PL成熟的DC能够直接激活有丝分裂原激活的蛋白激酶(MAPK),例如ERK1 / 2和p38,以及核转录因子NF-kappaB p65。同样,用NF-κBp65,ERK和p38 MAPK信号通路的抑制剂对DC进行预处理可抑制PL诱导的表面分子(如MHC II类和CD86)的上调以及IL-12的产生。我们的结果表明,PL刺激可以通过TLR2和/或TLR4介导的NF-κB,ERK和p38 MAPK信号通路诱导DC的表型和功能成熟。

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