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Glycosylation of Candida albicans Cell Wall Proteins Is Critical for Induction of Innate Immune Responses and Apoptosis of Epithelial Cells
C. albicans is one of the most common fungal pathogen of humans, causing local and superficial mucosal infections in immunocompromised individuals. Given that the key structure mediating host-C. albicans interactions is the fungal cell wall, we aimed to identify features of the cell wall inducing ep...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511564/ https://www.ncbi.nlm.nih.gov/pubmed/23226301 http://dx.doi.org/10.1371/journal.pone.0050518 |
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author | Wagener, Jeanette Weindl, Günther de Groot, Piet W. J. de Boer, Albert D. Kaesler, Susanne Thavaraj, Selvam Bader, Oliver Mailänder-Sanchez, Daniela Borelli, Claudia Weig, Michael Biedermann, Tilo Naglik, Julian R. Korting, Hans Christian Schaller, Martin |
author_facet | Wagener, Jeanette Weindl, Günther de Groot, Piet W. J. de Boer, Albert D. Kaesler, Susanne Thavaraj, Selvam Bader, Oliver Mailänder-Sanchez, Daniela Borelli, Claudia Weig, Michael Biedermann, Tilo Naglik, Julian R. Korting, Hans Christian Schaller, Martin |
author_sort | Wagener, Jeanette |
collection | PubMed |
description | C. albicans is one of the most common fungal pathogen of humans, causing local and superficial mucosal infections in immunocompromised individuals. Given that the key structure mediating host-C. albicans interactions is the fungal cell wall, we aimed to identify features of the cell wall inducing epithelial responses and be associated with fungal pathogenesis. We demonstrate here the importance of cell wall protein glycosylation in epithelial immune activation with a predominant role for the highly branched N-glycosylation residues. Moreover, these glycan moieties induce growth arrest and apoptosis of epithelial cells. Using an in vitro model of oral candidosis we demonstrate, that apoptosis induction by C. albicans wild-type occurs in early stage of infection and strongly depends on intact cell wall protein glycosylation. These novel findings demonstrate that glycosylation of the C. albicans cell wall proteins appears essential for modulation of epithelial immunity and apoptosis induction, both of which may promote fungal pathogenesis in vivo. |
format | Online Article Text |
id | pubmed-3511564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35115642012-12-05 Glycosylation of Candida albicans Cell Wall Proteins Is Critical for Induction of Innate Immune Responses and Apoptosis of Epithelial Cells Wagener, Jeanette Weindl, Günther de Groot, Piet W. J. de Boer, Albert D. Kaesler, Susanne Thavaraj, Selvam Bader, Oliver Mailänder-Sanchez, Daniela Borelli, Claudia Weig, Michael Biedermann, Tilo Naglik, Julian R. Korting, Hans Christian Schaller, Martin PLoS One Research Article C. albicans is one of the most common fungal pathogen of humans, causing local and superficial mucosal infections in immunocompromised individuals. Given that the key structure mediating host-C. albicans interactions is the fungal cell wall, we aimed to identify features of the cell wall inducing epithelial responses and be associated with fungal pathogenesis. We demonstrate here the importance of cell wall protein glycosylation in epithelial immune activation with a predominant role for the highly branched N-glycosylation residues. Moreover, these glycan moieties induce growth arrest and apoptosis of epithelial cells. Using an in vitro model of oral candidosis we demonstrate, that apoptosis induction by C. albicans wild-type occurs in early stage of infection and strongly depends on intact cell wall protein glycosylation. These novel findings demonstrate that glycosylation of the C. albicans cell wall proteins appears essential for modulation of epithelial immunity and apoptosis induction, both of which may promote fungal pathogenesis in vivo. Public Library of Science 2012-11-30 /pmc/articles/PMC3511564/ /pubmed/23226301 http://dx.doi.org/10.1371/journal.pone.0050518 Text en © 2012 Wagener et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Wagener, Jeanette Weindl, Günther de Groot, Piet W. J. de Boer, Albert D. Kaesler, Susanne Thavaraj, Selvam Bader, Oliver Mailänder-Sanchez, Daniela Borelli, Claudia Weig, Michael Biedermann, Tilo Naglik, Julian R. Korting, Hans Christian Schaller, Martin Glycosylation of Candida albicans Cell Wall Proteins Is Critical for Induction of Innate Immune Responses and Apoptosis of Epithelial Cells |
title | Glycosylation of Candida albicans Cell Wall Proteins Is Critical for Induction of Innate Immune Responses and Apoptosis of Epithelial Cells |
title_full | Glycosylation of Candida albicans Cell Wall Proteins Is Critical for Induction of Innate Immune Responses and Apoptosis of Epithelial Cells |
title_fullStr | Glycosylation of Candida albicans Cell Wall Proteins Is Critical for Induction of Innate Immune Responses and Apoptosis of Epithelial Cells |
title_full_unstemmed | Glycosylation of Candida albicans Cell Wall Proteins Is Critical for Induction of Innate Immune Responses and Apoptosis of Epithelial Cells |
title_short | Glycosylation of Candida albicans Cell Wall Proteins Is Critical for Induction of Innate Immune Responses and Apoptosis of Epithelial Cells |
title_sort | glycosylation of candida albicans cell wall proteins is critical for induction of innate immune responses and apoptosis of epithelial cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511564/ https://www.ncbi.nlm.nih.gov/pubmed/23226301 http://dx.doi.org/10.1371/journal.pone.0050518 |
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