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C-type lectin Langerin is a beta-glucan receptor on human Langerhans cells that recognizes opportunistic and
Marein A W P de Jong1, Lianne E M Vriend, Bart Theelen
1Center for Experimental and Molecular Medicine, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Abstract:
Langerhans cells (LCs) lining the stratified epithelia and mucosal tissues are the first antigen presenting cells to encounter invading pathogens, such as viruses, bacteria and fungi. Fungal infections form a health threat especially in immuno-compromised individuals. LCs express C-type lectin Langerin that has specificity for mannose, fucose and GlcNAc structures. Little is known about the role of human Langerin in fungal infections. Our data show that Langerin interacts with both mannan and beta-glucan structures, common cell-wall carbohydrate structures of fungi. We have screened a large panel of fungi for recognition by human Langerin and, strikingly, we observed strong binding of Langerin to a variety of Candida and Saccharomyces species and Malassezia furfur, but very weak binding was observed to Cryptococcus gattii and Cryptococcus neoformans. Notably, Langerin is the primary fungal receptor on LCs, since the interaction of LCs with the different fungi was blocked by antibodies against Langerin. Langerin recognizes both mannose and beta-glucans present on fungal cell walls and our data demonstrate that Langerin is the major fungal pathogen receptor on human LCs that recognizes pathogenic and commensal fungi. Together these data may provide more insight in the role of LCs in fungal infections.
Insights
Human Langerin, a receptor on Langerhans cells (LCs), binds to fungal cell walls, identifying key interactions in fungal infections. This research highlights Langerin
Area of Science:
- Immunology
- Microbiology
- Dermatology
Background:
- Langerhans cells (LCs) are crucial antigen-presenting cells at mucosal surfaces, encountering pathogens like fungi.
- Fungal infections pose significant risks, particularly to immunocompromised individuals.
- Human Langerin, expressed by LCs, recognizes specific carbohydrate structures on pathogens.
Purpose of the Study:
- To investigate the role of human Langerin in recognizing fungal pathogens.
- To determine which fungal species and cell wall components are recognized by Langerin.
Main Methods:
- Screening of a diverse fungal panel for binding to human Langerin.
- Utilizing antibodies against Langerin to block LC-fungal interactions.
- Analyzing fungal cell wall components, including mannan and beta-glucans.
Main Results:
- Human Langerin demonstrated strong binding to Candida, Saccharomyces, and Malassezia furfur species.
- Weak binding was observed with Cryptococcus gattii and Cryptococcus neoformans.
- Langerin was identified as the primary receptor mediating LC recognition of these fungi.
Conclusions:
- Langerin recognizes both mannose and beta-glucan structures on fungal cell walls.
- Langerin is the major receptor on human LCs for recognizing a variety of pathogenic and commensal fungi.
- These findings provide insights into the role of LCs in host defense against fungal infections.
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