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Candida albicans induces neutrophil extracellular traps and leucotoxic hypercitrullination via candidalysin
The peptide toxin candidalysin, secreted by Candida albicans hyphae, promotes stimulation of neutrophil extracellular traps (NETs). However, candidalysin alone triggers a distinct mechanism for NET‐like structures (NLS), which are more compact and less fibrous than canonical NETs. Candidalysin activ...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10626426/ https://www.ncbi.nlm.nih.gov/pubmed/37795769 http://dx.doi.org/10.15252/embr.202357571 |
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author | Unger, Lucas Skoluda, Samuel Backman, Emelie Amulic, Borko Ponce‐Garcia, Fernando M Etiaba, Chinelo NC Yellagunda, Sujan Krüger, Renate von Bernuth, Horst Bylund, Johan Hube, Bernhard Naglik, Julian R Urban, Constantin F |
author_facet | Unger, Lucas Skoluda, Samuel Backman, Emelie Amulic, Borko Ponce‐Garcia, Fernando M Etiaba, Chinelo NC Yellagunda, Sujan Krüger, Renate von Bernuth, Horst Bylund, Johan Hube, Bernhard Naglik, Julian R Urban, Constantin F |
author_sort | Unger, Lucas |
collection | PubMed |
description | The peptide toxin candidalysin, secreted by Candida albicans hyphae, promotes stimulation of neutrophil extracellular traps (NETs). However, candidalysin alone triggers a distinct mechanism for NET‐like structures (NLS), which are more compact and less fibrous than canonical NETs. Candidalysin activates NADPH oxidase and calcium influx, with both processes contributing to morphological changes in neutrophils resulting in NLS formation. NLS are induced by leucotoxic hypercitrullination, which is governed by calcium‐induced protein arginine deaminase 4 activation and initiation of intracellular signalling events in a dose‐ and time‐dependent manner. However, activation of signalling by candidalysin does not suffice to trigger downstream events essential for NET formation, as demonstrated by lack of lamin A/C phosphorylation, an event required for activation of cyclin‐dependent kinases that are crucial for NET release. Candidalysin‐triggered NLS demonstrate anti‐Candida activity, which is resistant to nuclease treatment and dependent on the deprivation of Zn(2+). This study reveals that C. albicans hyphae releasing candidalysin concurrently trigger canonical NETs and NLS, which together form a fibrous sticky network that entangles C. albicans hyphae and efficiently inhibits their growth. |
format | Online Article Text |
id | pubmed-10626426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106264262023-11-07 Candida albicans induces neutrophil extracellular traps and leucotoxic hypercitrullination via candidalysin Unger, Lucas Skoluda, Samuel Backman, Emelie Amulic, Borko Ponce‐Garcia, Fernando M Etiaba, Chinelo NC Yellagunda, Sujan Krüger, Renate von Bernuth, Horst Bylund, Johan Hube, Bernhard Naglik, Julian R Urban, Constantin F EMBO Rep Articles The peptide toxin candidalysin, secreted by Candida albicans hyphae, promotes stimulation of neutrophil extracellular traps (NETs). However, candidalysin alone triggers a distinct mechanism for NET‐like structures (NLS), which are more compact and less fibrous than canonical NETs. Candidalysin activates NADPH oxidase and calcium influx, with both processes contributing to morphological changes in neutrophils resulting in NLS formation. NLS are induced by leucotoxic hypercitrullination, which is governed by calcium‐induced protein arginine deaminase 4 activation and initiation of intracellular signalling events in a dose‐ and time‐dependent manner. However, activation of signalling by candidalysin does not suffice to trigger downstream events essential for NET formation, as demonstrated by lack of lamin A/C phosphorylation, an event required for activation of cyclin‐dependent kinases that are crucial for NET release. Candidalysin‐triggered NLS demonstrate anti‐Candida activity, which is resistant to nuclease treatment and dependent on the deprivation of Zn(2+). This study reveals that C. albicans hyphae releasing candidalysin concurrently trigger canonical NETs and NLS, which together form a fibrous sticky network that entangles C. albicans hyphae and efficiently inhibits their growth. John Wiley and Sons Inc. 2023-10-05 /pmc/articles/PMC10626426/ /pubmed/37795769 http://dx.doi.org/10.15252/embr.202357571 Text en © 2023 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Unger, Lucas Skoluda, Samuel Backman, Emelie Amulic, Borko Ponce‐Garcia, Fernando M Etiaba, Chinelo NC Yellagunda, Sujan Krüger, Renate von Bernuth, Horst Bylund, Johan Hube, Bernhard Naglik, Julian R Urban, Constantin F Candida albicans induces neutrophil extracellular traps and leucotoxic hypercitrullination via candidalysin |
title |
Candida albicans induces neutrophil extracellular traps and leucotoxic hypercitrullination via candidalysin |
title_full |
Candida albicans induces neutrophil extracellular traps and leucotoxic hypercitrullination via candidalysin |
title_fullStr |
Candida albicans induces neutrophil extracellular traps and leucotoxic hypercitrullination via candidalysin |
title_full_unstemmed |
Candida albicans induces neutrophil extracellular traps and leucotoxic hypercitrullination via candidalysin |
title_short |
Candida albicans induces neutrophil extracellular traps and leucotoxic hypercitrullination via candidalysin |
title_sort | candida albicans induces neutrophil extracellular traps and leucotoxic hypercitrullination via candidalysin |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10626426/ https://www.ncbi.nlm.nih.gov/pubmed/37795769 http://dx.doi.org/10.15252/embr.202357571 |
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