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首页> 外文期刊>The journal of immunology >Dendritic Cell-Specific Intercellular Adhesion Molecule 3-Grabbing Nonintegrin Mediates Binding and Internalization of Aspergillus fumigatus Conidia by Dendritic Cells and Macrophages
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Dendritic Cell-Specific Intercellular Adhesion Molecule 3-Grabbing Nonintegrin Mediates Binding and Internalization of Aspergillus fumigatus Conidia by Dendritic Cells and Macrophages

机译:树突状细胞特定的细胞间粘附分子3抓住nonintegrin介导树突状细胞和巨噬细胞对烟曲霉分生孢子的结合和内在化。

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Aspergillus fumigatus is responsible for a large percentage of nosocomial opportunistic fungal infections in immunocompromised hosts, especially during cytotoxic chemotherapy and after bone marrow transplantation, and is currently a major direct cause of death in leukemia patients. Dendritic cell-specific ICAM-3-grabbing nonintegrin (DC-SIGN) is a type II C-type lectin that functions as an adhesion receptor and is used by viral and bacterial pathogens to gain access to human DC. We report that DC-SIGN specifically interacts with clinical isolates of A. fumigatus . DC-SIGN-dependent binding of A. fumigatus conidia can be demonstrated with stable transfectants and monocyte-derived DC and is inhibited by anti-DC-SIGN Abs. Binding and internalization of A. fumigatus conidia correlates with DC-SIGN cell surface expression levels and is abolished in the presence of A. funigatus -derived cell wall galactomannans. The clinical relevance of this interaction is emphasized by the presence of DC-SIGN in lung DC and alveolar macrophages, and further illustrated by the DC-SIGN-dependent attachment of A. fumigatus conidia to the cell membrane of IL-4-treated monocyte-derived macrophages. Our results suggest the involvement of DC-SIGN in the initial stages of pulmonary infection as well as in fungal spreading during invasive aspergillosis.
机译:烟曲霉是免疫受损宿主中很大比例的医院机会性真菌感染的原因,尤其是在细胞毒性化疗期间和骨髓移植后,目前是白血病患者死亡的主要直接原因。树突状细胞特异性ICAM-3-夺取非整联蛋白(DC-SIGN)是II型C型凝集素,起粘附受体的作用,被病毒和细菌病原体用来获得人类DC。我们报告DC-SIGN专门与烟曲霉的临床分离物相互作用。可以用稳定的转染子和单核细胞衍生的DC证明烟曲霉孢子的DC-SIGN依赖性结合,并被抗DC-SIGN Abs抑制。烟曲霉分生孢子的结合和内在化与DC-SIGN细胞表面表达水平相关,并且在存在源自真菌曲霉的细胞壁半乳甘露聚糖中被消除。肺DC和肺泡巨噬细胞中DC-SIGN的存在强调了这种相互作用的临床相关性,烟曲霉分生孢子对IL-4处理的单核细胞衍生的巨噬细胞。我们的结果表明DC-SIGN参与了肺部感染的初期以及侵袭性曲霉病期间的真菌扩散。

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