Literature DB >> 24286790

Induction of innate immunity by Aspergillus fumigatus cell wall polysaccharides is enhanced by the composite presentation of chitin and beta-glucan.

Lalit Kumar Dubey1, Jesper Bonnet Moeller1, Anders Schlosser1, Grith Lykke Sorensen1, Uffe Holmskov2.   

Abstract

Chitin and β-glucan are conserved throughout evolution in the fungal cell wall and are the most common polysaccharides in fungal species. Together, these two polysaccharides form a structural scaffold that is essential for the survival of the fungus. In the present study, we demonstrated that Aspergillus fumigatus alkali-insoluble cell wall fragments (AIF), composed of chitin linked covalently to β-glucan, induced enhanced immune responses when compared with individual cell wall polysaccharides. Intranasal administration of AIF induced eosinophil and neutrophil recruitment, chitinase activity, TNF-α and TSLP production in mice lungs. Selective destruction of chitin or β-glucan from AIF significantly reduced eosinophil and neutrophil recruitment as well as chitinase activity and cytokine expression by macrophages, indicating the synergistic effect of the cell wall polysaccharides when presented together as a composite PAMP. We also showed that these cell wall polysaccharides induced chitin-specific IgM in mouse serum. Our in vivo and in vitro data indicate that chitin and β-glucan play important roles in activating innate immunity when presented as composite cell wall PAMPs.
Copyright © 2013. Published by Elsevier GmbH.

Entities:  

Keywords:  A. fumigatus; ABPA; AIF; AMCase; Aspergillus fumigatus; BAL; Chitin; FReD; Fungal cell wall polysaccharides; GlcNAc; Inflammation; Innate immunity; Lung; N-acetylglucosamine; PAMPs; PRRs; acidic mammalian chitinase; alkali-insoluble cell wall fragments; allergic bronchopulmonary aspergillosis; bronchoalveolar lavage; fibrinogen-related domain; pathogen-associated molecular patterns; pattern recognition receptors; β-Glucan

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Substances:

Year:  2013        PMID: 24286790     DOI: 10.1016/j.imbio.2013.10.003

Source DB:  PubMed          Journal:  Immunobiology        ISSN: 0171-2985            Impact factor:   3.144


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