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蟑螂过敏原与甘露糖受体(CD206)在人循环纤维细胞中的功能相互作用。

Functional interaction of cockroach allergens and mannose receptor (CD206) in human circulating fibrocytes.

机构信息

Johns Hopkins Asthma and Allergy Center, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

出版信息

PLoS One. 2013 May 29;8(5):e64105. doi: 10.1371/journal.pone.0064105. Print 2013.

Abstract

BACKGROUND

The innate pattern recognition C-type-lectin receptors (CLRs), including mannose receptor (MRC1; CD206), have been suggested to functionally interact with allergens and are critical in controlling immune response. Fibrocytes have been considered to play a role in allergic asthma. Here we sought to investigate the functional interaction of cockroach allergens with CD206 in fibrocytes.

METHODS

Profiling of N-linked glycans from natural purified cockroach allergen Bla g 2 was accomplished by MALDI-MS. The binding activity of cockroach allergens to CD206 was determined by solid-phase binding assays. Levels of CD206 expression on human fibrocytes and CD206 mediated signaling and cytokine production in Bla g 2 treated fibrocytes were determined.

RESULTS

Profiling of N-linked glycans from Bla g 2 revealed a predominance of small, mannose-terminated glycans with and without fucose. Significant binding of Bla g 2 to CD206 was observed, which was inhibited by yeast mannan (a known CD206 ligand), free mannose, and a blocking antibody (anti-hMR). Flow cytometric analyses of human fibrocytes (CD45(+) and collagen-1(+)) showed selective expression of CD206 on fibrocytes. Functionally, a concentration-dependent uptake of FITC labeled Bla g 2 by fibrocytes was observed, but was significantly inhibited by anti-hMR. Bla g 2 can stimulate up-regulation of inflammatory cytokines including TNF-alpha and IL-6 and activation of nuclear factor kappa B (NF-kB/p65), p38 mitogen-activated protein kinase (p38), ERK, and JNK in cultured fibrocytes. This increased secretion of TNF-alpha and IL-6 and activation of NF-kB, ERK, and JNK was significantly inhibited by the addition of either mannan or mannose. Furthermore, Bla g 2 induced increase in TNF-alpha and IL-6 production was also inhibited by the use of NF-kB, ERK, and JNK inhibitors.

CONCLUSION

These results provide evidence supporting the existence of a functional cockroach allergen-CD206 axis in human fibrocytes, suggesting a role for CD206 in regulating allergen induced allergic responses in asthma.

摘要

背景

先天模式识别 C 型凝集素受体(CLRs),包括甘露糖受体(MRC1;CD206),已被认为在功能上与过敏原相互作用,并且在控制免疫反应中至关重要。纤维细胞被认为在过敏性哮喘中发挥作用。在这里,我们试图研究蟑螂过敏原与纤维细胞中的 CD206 的功能相互作用。

方法

通过 MALDI-MS 对天然纯化的蟑螂过敏原 Bla g 2 的 N-连接糖进行分析。通过固相结合测定法确定蟑螂过敏原与 CD206 的结合活性。测定人纤维细胞中 CD206 的表达水平以及 Bla g 2 处理的纤维细胞中 CD206 介导的信号转导和细胞因子产生。

结果

对 Bla g 2 的 N-连接糖进行分析显示,小的、以甘露糖结尾的糖和没有岩藻糖的糖占主导地位。观察到 Bla g 2 与 CD206 有明显的结合,这种结合被酵母甘露聚糖(已知的 CD206 配体)、游离甘露糖和阻断抗体(抗 hMR)抑制。对人纤维细胞(CD45(+)和胶原蛋白-1(+))的流式细胞分析显示,纤维细胞上选择性表达 CD206。功能上,观察到 FITC 标记的 Bla g 2 被纤维细胞的浓度依赖性摄取,但用抗 hMR 显著抑制。Bla g 2 可刺激培养的纤维细胞中炎症细胞因子(包括 TNF-α和 IL-6)和核因子 kappa B(NF-kB/p65)、p38 丝裂原激活蛋白激酶(p38)、ERK 和 JNK 的上调。这种 TNF-α和 IL-6 的分泌增加以及 NF-kB、ERK 和 JNK 的激活,在用甘露聚糖或甘露糖处理后显著受到抑制。此外,Bla g 2 诱导的 TNF-α和 IL-6 产生增加也被 NF-kB、ERK 和 JNK 抑制剂抑制。

结论

这些结果提供了支持人类纤维细胞中存在功能性蟑螂过敏原-CD206 轴的证据,表明 CD206 在调节哮喘中过敏原诱导的过敏反应中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc1e/3667076/c142ba5db983/pone.0064105.g001.jpg

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