Johns Hopkins Asthma and Allergy Center, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
PLoS One. 2013 May 29;8(5):e64105. doi: 10.1371/journal.pone.0064105. Print 2013.
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.
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.
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.
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.
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。
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。
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。
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。