首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >A homogalacturonan from Hippophae rhamnoides L. Berries enhance immunomodulatory activity through TLR4/MyD88 pathway mediated activation of macrophages
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A homogalacturonan from Hippophae rhamnoides L. Berries enhance immunomodulatory activity through TLR4/MyD88 pathway mediated activation of macrophages

机译:来自Hippophae rhamnoides L.浆果的HomogalactuRonan通过TLR4 / MyD88介导的巨噬细胞活化增强免疫调节活性

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Our previous study isolated a natural high-methoxyl homogalacturonan (HRWP-A) from Hippophae rhamnoides and showed antitumor activity in vivo. In this study, the immunomodulatory activity and mechanisms of action of HRWP-A were further investigated. Results showed that HRWP-A could recover the body condition and activated macrophage in Cyclophosphamide (CTX)-induced immunosuppressed mice. Further, we investigated the possible mechanism underlying the effects of HRWP-A on mouse peritoneal macrophages. qPCR and western blot revealed that HRWP-A upregulated the expression of TLR4 mRNA in vitro. This process was accompanied by a clear increase in MyD88 expression and p-l kappa B-alpha, but these effects were largely abrogated by pretreatment with anti-TLR4 antibodies. The effects of HRWP-A on macrophage NO, IL-1 beta and 1L-6 production were also inhibited by anti-TLR4 antibodies and were greatly influenced by the NF-kappa B inhibitor PDTC. Moreover, HRWP-A failed to induce the production of NO, IL-1 beta and IL-6 in peritoneal macrophages prepared from C3H/HeJ mice, which have a point mutation in the Tlr4 gene, suggesting the involvement of the TLR4 molecule in HRWP-A-mediated macrophage activation. These results may have important implications for our understanding of the structure-activity relationship of immunopotentiating polysaccharides from medicinal herbs. (C) 2017 Elsevier B.V. All rights reserved.
机译:我们以前的研究从Hippophae ramnoides中分离出天然高甲氧基同源肌炎(HRWP-A),并在体内显示抗肿瘤活性。在该研究中,进一步研究了免疫调节活性和HRWP-A的作用机制。结果表明,HRWP-A可以在环磷酰胺(CTX)诱导的免疫抑制小鼠中恢复体状和活化巨噬细胞。此外,我们研究了HRWP-A对小鼠腹膜巨噬细胞的影响的可能机制。 QPCR和Western印迹显示HRWP-A上调TLR4 mRNA在体外表达。该方法伴随着MyD88表达和P-L Kappa B-α的明显增加,但是通过用抗TLR4抗体预处理,这些效果大大消除。 HRWP-A对巨噬细胞NO,IL-1β和1L-6产生的影响也受到抗TLR4抗体抑制的,并且受到NF-Kappa B抑制剂PDTC的大大影响。此外,HRWP-A未能诱导由C3H / HEJ小鼠制备的腹膜巨噬细胞的NO,IL-1β和IL-6的产生,其在TLR4基因中具有点突变,表明TLR4分子在HRWP中的参与-A介导的巨噬细胞激活。这些结果可能对我们对来自药草免疫增强多糖的结构 - 活性关系的理解具有重要意义。 (c)2017年Elsevier B.V.保留所有权利。

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