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Quantification of zinc intoxication of Candida glabrata after phagocytosis by primary macrophages

Zinc (Zn(2+)) is a trace element, playing pivotal roles during host-pathogen interactions. Macrophages can sequester Zn(2+) and restrict bioavailability or increase phagolysosomal Zn(2+) to kill pathogens. This method quantifies Zn(2+)-mediated clearance of the human fungal pathogen C. glabrata afte...

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Autores principales: Penninger, Philipp, Riedelberger, Michael, Tsymala, Irina, Arzani, Hossein, Jenull, Sabrina, Kuchler, Karl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907919/
https://www.ncbi.nlm.nih.gov/pubmed/33665632
http://dx.doi.org/10.1016/j.xpro.2021.100352
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author Penninger, Philipp
Riedelberger, Michael
Tsymala, Irina
Arzani, Hossein
Jenull, Sabrina
Kuchler, Karl
author_facet Penninger, Philipp
Riedelberger, Michael
Tsymala, Irina
Arzani, Hossein
Jenull, Sabrina
Kuchler, Karl
author_sort Penninger, Philipp
collection PubMed
description Zinc (Zn(2+)) is a trace element, playing pivotal roles during host-pathogen interactions. Macrophages can sequester Zn(2+) and restrict bioavailability or increase phagolysosomal Zn(2+) to kill pathogens. This method quantifies Zn(2+)-mediated clearance of the human fungal pathogen C. glabrata after phagocytosis by innate immune cells. Double staining with propidium iodide and a zinc-specific fluorescence dye allows for discrimination of live versus dead pathogens inside phagolysosomes. Moreover, elevated phagolysosomal Zn(2+) decreases fungal viability as a function of intracellular Zn(2+) concentrations in macrophages. For complete details on the use and execution of this protocol, please refer to Riedelberger et al. (2020).
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spelling pubmed-79079192021-03-03 Quantification of zinc intoxication of Candida glabrata after phagocytosis by primary macrophages Penninger, Philipp Riedelberger, Michael Tsymala, Irina Arzani, Hossein Jenull, Sabrina Kuchler, Karl STAR Protoc Protocol Zinc (Zn(2+)) is a trace element, playing pivotal roles during host-pathogen interactions. Macrophages can sequester Zn(2+) and restrict bioavailability or increase phagolysosomal Zn(2+) to kill pathogens. This method quantifies Zn(2+)-mediated clearance of the human fungal pathogen C. glabrata after phagocytosis by innate immune cells. Double staining with propidium iodide and a zinc-specific fluorescence dye allows for discrimination of live versus dead pathogens inside phagolysosomes. Moreover, elevated phagolysosomal Zn(2+) decreases fungal viability as a function of intracellular Zn(2+) concentrations in macrophages. For complete details on the use and execution of this protocol, please refer to Riedelberger et al. (2020). Elsevier 2021-02-20 /pmc/articles/PMC7907919/ /pubmed/33665632 http://dx.doi.org/10.1016/j.xpro.2021.100352 Text en © 2021. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Penninger, Philipp
Riedelberger, Michael
Tsymala, Irina
Arzani, Hossein
Jenull, Sabrina
Kuchler, Karl
Quantification of zinc intoxication of Candida glabrata after phagocytosis by primary macrophages
title Quantification of zinc intoxication of Candida glabrata after phagocytosis by primary macrophages
title_full Quantification of zinc intoxication of Candida glabrata after phagocytosis by primary macrophages
title_fullStr Quantification of zinc intoxication of Candida glabrata after phagocytosis by primary macrophages
title_full_unstemmed Quantification of zinc intoxication of Candida glabrata after phagocytosis by primary macrophages
title_short Quantification of zinc intoxication of Candida glabrata after phagocytosis by primary macrophages
title_sort quantification of zinc intoxication of candida glabrata after phagocytosis by primary macrophages
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907919/
https://www.ncbi.nlm.nih.gov/pubmed/33665632
http://dx.doi.org/10.1016/j.xpro.2021.100352
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