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首页> 外文期刊>Bioconjugate Chemistry >beta-Glucan Grafted Microcapsule, a Tool for Studying the Immunomodulatory Effect of Microbial Cell Wall Polysaccharides
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beta-Glucan Grafted Microcapsule, a Tool for Studying the Immunomodulatory Effect of Microbial Cell Wall Polysaccharides

机译:β-葡聚糖接枝微胶囊,一种用于研究微生物细胞壁多糖的免疫调节作用的工具

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摘要

beta-(1,3)-Glucan is one of the antigenic components of the bacterial as well as fungal cell wall. We designed microcapsules (MCs) ligated with beta-(1,3)-glucan, to study its immunomodulatory effect. The MCs were obtained by interfacial polycondensation between diacyl chloride (sebacoyl chloride and terephtaloyl chloride) and diethylenetriamine in organic and aqueous phases, respectively. Planar films were first designed to optimize monomer compositions and to examine the kinetics of film formation. MCs with aqueous fluorescent core were then obtained upon controlled emulsification-polycondensation reactions using optimized monomer compositions and adding fluorescein into the aqueous phase. The selected MC-formulation was grafted with Curdlan, a linear beta-(1,3)glucan from Agrobacterium species or branched beta-(1,3)-glucan isolated from the cell wall of Aspergillus fumigatus. These beta-(1,3)-glucan grafted MCs were phagocytosed by human monocyte-derived macrophages, and stimulated cytokine secretion. Moreover, the blocking of dectin-1, a beta-(1,3)-glucan recognizing receptor, did not completely inhibit the phagocytosis of these beta-(1,3)-glucan grafted MCs, suggesting the involvement of other receptors in the recognition and uptake of beta-(1,3)-glucan. Overall, grafted MCs are a useful tool for the study of the mechanism of phagocytosis and immunomodulatory effect of the microbial polysaccharides.
机译:β-(1,3)-Glucan是细菌和真菌细胞壁的抗原组分之一。我们设计了用β-(1,3)-Glucan连接的微胶囊(MCS),以研究其免疫调节效果。通过分枝酰氯(SebaCoyl氯和氯化甲酰氯)与有机和水相的二亚乙基三胺的界面缩聚获得MCS。首先设计平面薄膜以优化单体组合物并检查膜形成的动力学。然后使用优化的单体组合物在受控乳化缩聚反应下得到具有含水荧光核的MCs,并将荧光素添加到水相中。将所选择的MC-制剂用Curdlan接枝,来自农杆菌物种的线性β-(1,3)葡聚糖或从曲霉属Fumigatus的细胞壁中分离的葡萄糖β-(1,3)。这些β-(1,3)-Glucan接枝MCS被人单核细胞衍生的巨噬细胞吞噬,刺激细胞因子分泌。此外,Dectin-1的阻断,β-(1,3)识别受体的β-(1,3),并没有完全抑制这些β-(1,3)葡萄糖接枝MCS的吞噬作用,表明其他受体参与其中β-(1,3)葡萄糖的识别和摄取。总体而言,接枝MCS是研究微生物多糖的吞噬作用和免疫调节作用的机制的有用工具。

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  • 来源
    《Bioconjugate Chemistry 》 |2019年第6期| 共10页
  • 作者单位

    Univ Paris Saclay Univ Paris Sud Fac Pharm Inst Galien Paris Sud CNRS UMR 8612 F-92296 Chatenay Malabry France;

    Inst Pasteur Unite Aspergillus F-75015 Paris France;

    Univ Paris Saclay Univ Paris Sud Fac Pharm Inst Galien Paris Sud CNRS UMR 8612 F-92296 Chatenay Malabry France;

    Univ Aberdeen Aberdeen Fungal Grp MRC Ctr Med Mycol Aberdeen AB25 2ZD Scotland;

    Inst Pasteur Unite Aspergillus F-75015 Paris France;

    Inst Pasteur Unite Aspergillus F-75015 Paris France;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学 ;
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