Mohamed Emara
Recognition of the major cat allergen Fel d 1 through the cysteine-rich domain of the mannose receptor determines its allergenicity
Emara, Mohamed; Royer, Pierre Joseph; Abbas, Zaigham; Sewell, Herb F.; Gebriel Mohamed, Gihan; Singh, Sonali; Peel, Samantha; Fox, Jane; Shakib, Farouk; Martinez-Pomares, Luisa; Ghaemmaghami, Amir M.
Authors
Pierre Joseph Royer
Zaigham Abbas
Herb F. Sewell
Gihan Gebriel Mohamed
Dr SONALI SINGH SONALI.SINGH@NOTTINGHAM.AC.UK
Research Development Manager
Samantha Peel
Jane Fox
Farouk Shakib
Professor LUISA MARTINEZ-POMARES LUISA.M@NOTTINGHAM.AC.UK
PROFESSOR OF INNATE IMMUNITY AND INFLAMMATION
Professor AMIR GHAEMMAGHAMI AMIR.GHAEMMAGHAMI@NOTTINGHAM.AC.UK
PROFESSOR OF IMMUNOLOGY AND IMMUNO- BIOENGINEERING
Abstract
Dendritic cells are professional antigen-presenting cells that are specialized in antigen uptake and presentation. Allergy to cat has increased substantially in recent years and has been shown to be positively associated with asthma.Wehave recently shown that the mannose receptor (MR), a C-type lectin expressed by dendritic cells, recognizes various glycoallergens from diverse sources and is involved in promoting allergic responses to a major house dust mite allergen in vitro. Here we investigated the potential role of MR in allergic responses to Fel d 1, a major cat allergen. Fel d 1 binding to MR was confirmed by ELISA. Using blocking, gene silencing (siRNA) experiments, and MR knock-out (MR-/-) cells, we have demonstrated that MRplays a major role in internalization of Fel d 1 by human and mouse antigen-presenting cells. Intriguingly, unlike other glycoallergens, recognition of Fel d 1 by MR is mediated by the cysteine-rich domain, which correlates with the presence of sulfated carbohydrates in natural Fel d 1. WT and MR-/- mice were used to study the role of MR in allergic sensitization to Fel d 1 in vivo. MR-/- mice sensitized with cat dander extract and Fel d 1 produced significantly lower levels of total IgE, Fel d 1-specific-IgE and IgG1, the hallmarks of allergic response, compared with WT mice. Our data show for the first time that Fel d 1 is a novel ligand of the cysteine-rich domain of MR and that MR is likely to play a pivotal role in allergic sensitization to airborne allergens in vivo. © 2011 by The American Society for Biochemistry and Molecular Biology, Inc.
Citation
Emara, M., Royer, P. J., Abbas, Z., Sewell, H. F., Gebriel Mohamed, G., Singh, S., Peel, S., Fox, J., Shakib, F., Martinez-Pomares, L., & Ghaemmaghami, A. M. (2011). Recognition of the major cat allergen Fel d 1 through the cysteine-rich domain of the mannose receptor determines its allergenicity. Journal of Biological Chemistry, 286(15), 13033-13040. https://doi.org/10.1074/jbc.M111.220657
Journal Article Type | Article |
---|---|
Publication Date | Apr 15, 2011 |
Deposit Date | Jan 3, 2023 |
Publicly Available Date | Jan 27, 2023 |
Journal | Journal of Biological Chemistry |
Print ISSN | 0021-9258 |
Electronic ISSN | 1083-351X |
Publisher | American Society for Biochemistry and Molecular Biology |
Peer Reviewed | Peer Reviewed |
Volume | 286 |
Issue | 15 |
Pages | 13033-13040 |
DOI | https://doi.org/10.1074/jbc.M111.220657 |
Public URL | https://nottingham-repository.worktribe.com/output/3097534 |
Publisher URL | https://www.jbc.org/article/S0021-9258(20)51684-0/fulltext#seccestitle10 |
Files
Recognition of the Major Cat Allergen Fel d 1 through the Cysteine-rich Domain of the Mannose Receptor Determines Its Allergenicity
(1.1 Mb)
PDF
Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
You might also like
Identification of Pseudomonas aeruginosa exopolysaccharide Psl in biofilms using 3D OrbiSIMS
(2023)
Journal Article
Development of dual anti-biofilm and anti-bacterial medical devices
(2020)
Journal Article
Downloadable Citations
About Repository@Nottingham
Administrator e-mail: discovery-access-systems@nottingham.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2025
Advanced Search