Abstract

BackgroundThe 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.MethodsProfiling 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.ResultsProfiling 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.ConclusionThese 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.

Highlights

  • Asthma is the leading serious chronic illness of children in the US

  • Glycan compositions were assigned by comparison of measured m/z values with m/z values calculated based on putative composition of native glycans using the Functional Glycomics glycan database and SimGlycan software (Premier Biosoft, Palo Alto, CA) [46]

  • We found that natural purified cockroach allergen Bla g 2 contains putative structures that have a significant amount of glycans, and many of these terminate with mannose

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Summary

Introduction

Asthma is the leading serious chronic illness of children in the US. Exposure to cockroach allergen in early life can lead to allergic sensitization and increase the risk of developing asthma [1,2,3,4]. Recent studies in the New York City Neighborhood Asthma and Allergy Study (NAAS) have found that cockroach allergen (Bla g 2) was more prevalent in bed dust from homes in high asthma prevalence neighborhoods (HAPN) than that from low asthma prevalence neighborhoods (LAPN) [6]. These studies support the notion that cockroach exposure increases the risk of allergic sensitization, which in turn leads to the development of asthma. We sought to investigate the functional interaction of cockroach allergens with CD206 in fibrocytes

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