The glycosylation pattern of common allergens: The recognition and uptake of Der p 1 by epithelial and dendritic cells is carbohydrate dependent

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Abstract

Allergens are initiators of both innate and adaptive immune responses. They are recognised at the site of entry by epithelial and dendritic cells (DCs), both of which activate innate inflammatory circuits that can collectively induce Th2 immune responses. In an attempt to have a better understanding of the role of carbohydrates in the recognition and uptake of allergens by the innate immune system, we defined common glycosylation patterns in major allergens. This was done using labelled lectins and showed that allergens like Der p 1 (Dermatophagoides pteronyssinus group 1), Fel d 1 (Felis domisticus), Ara h 1 (Arachis hypogaea), Der p 2 (Dermatophagoides pteronyssinus group 2), Bla g 2 (Blattella germanica) and Can f 1 (Canis familiaris) are glycosylated and that the main dominant sugars on these allergens are 1-2, 1-3 and 1-6 mannose. These observations are in line with recent reports implicating the mannose receptor (MR) in allergen recognition and uptake by DCs and suggesting a major link between glycosylation and allergen recognition. We then looked at TSLP (Thymic Stromal Lymphopoietin) cytokine secretion by lung epithelia upon encountering natural Der p 1 allergen. TSLP is suggested to drive DC maturation in support of allergic hypersensitivity reactions. Our data showed an increase in TSLP secretion by lung epithelia upon stimulation with natural Der p 1 which was carbohydrate dependent. The deglycosylated preparation of Der p 1 exhibited minimal uptake by DCs compared to the natural and hyperglycosylated recombinant counterparts, with the latter being taken up more readily than the other preparations. Collectively, our data indicate that carbohydrate moieties on allergens play a vital role in their recognition by innate immune cells, implicating them in downstream deleterious Th2 cell activation and IgE production. © 2012 Al-Ghouleh et al.

Figures

  • Table 1. Western blot results of different lectin reactions with different allergens.
  • Figure 1. Comparative analysis of cysteine protease allergens and non-allergens in terms of mannosylation. Allergens are strongly mannosylated and have stronger reaction with anti-mannose GNA compared to non-allergens. +++: strong reaction, ++: moderate reaction, +: mild reaction, 2: no reaction. doi:10.1371/journal.pone.0033929.g001
  • Figure 2. MFI ± SEM readings which represent the difference in uptake between natural and recombinant Der p 1 (1 mg/ml) by immature DCs. There was a significant difference between natural and recombinant allergen uptake. The results suggest that the average mean of uptake for the recombinant preparation is higher than that for natural Der p 1. The results also show that the uptake of Der p 1 by immature DCs at 4uC is lower than the uptake at 37uC for both preparations. Both natural and recombinant Der p 1 were labelled with FITC. *P value,0.05. doi:10.1371/journal.pone.0033929.g002
  • Figure 3. Confocal images of the difference between recombinant and natural Der p 1 (0.5 mg/ml) uptake by the same immature DC at 376C. The results suggest that the uptake of the recombinant preparation (A) is higher than that for natural Der p 1 (B) in the same DC. A. Green: rDer p 1 labelled with FITC, red: MR labelled with PE, blue: nucleus labelled with DAPI. B. Green: nDer p 1 labelled with Cy5, red: MR labelled with PE, blue: nucleus labelled with DAPI. doi:10.1371/journal.pone.0033929.g003
  • Figure 4. A. Natural and recombinant Der p 1 uptake by immature DCs at 37uC compared to the non-allergen Staphopain B at the same conditions and concentrations. Results presented as MFI 6 SDM and all preparations were labelled with FITC. B. Confocal images of the uptake of Staphopain B by immature DCs. doi:10.1371/journal.pone.0033929.g004
  • Figure 5. The uptake of recombinant and natural preparations of Der p 1 (1 mg/ml) by immature DCs at 30 mins. A. Green: rDer p1 stained with FITC, red: MR stained with PE, blue: nucleus stained with DAPI. B. Green: nDer p 1 stained with Cy5, red: MR stained with PE, blue: nucleus stained with DAPI. doi:10.1371/journal.pone.0033929.g005
  • Figure 6. The co-localization of natural and recombinant Derp1 (0.5 mg/ml) with LAMP-2 detected at 10 mins. A. Green: rDer p 1 stained with FITC, red: LAMP-2 stained with PE, blue: nucleus stained with DAPI. B. Green: nDer p 1 stained with Cy5, red: LAMP-2 stained with PE, blue: nucleus stained with DAPI. doi:10.1371/journal.pone.0033929.g006
  • Figure 7. Western blot against GNA (anti-mannose) of natural and recombinant Der p 1 before and after periodate treatment.

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APA

Al-Ghouleh, A., Johal, R., Sharquie, I. K., Emara, M., Harrington, H., Shakib, F., & Ghaemmaghami, A. M. (2012). The glycosylation pattern of common allergens: The recognition and uptake of Der p 1 by epithelial and dendritic cells is carbohydrate dependent. PLoS ONE, 7(3). https://doi.org/10.1371/journal.pone.0033929

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