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A transgenic zebrafish line for in vivo visualisation of neutrophil myeloperoxidase

The neutrophil enzyme myeloperoxidase (MPO) is a major enzyme made by neutrophils to generate antimicrobial and immunomodulatory compounds, notably hypochlorous acid (HOCl), amplifying their capacity for destroying pathogens and regulating inflammation. Despite its roles in innate immunity, the impo...

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Autores principales: Buchan, Kyle D., Prajsnar, Tomasz K., Ogryzko, Nikolay V., de Jong, Nienke W. M., van Gent, Michiel, Kolata, Julia, Foster, Simon J., van Strijp, Jos A. G., Renshaw, Stephen A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474608/
https://www.ncbi.nlm.nih.gov/pubmed/31002727
http://dx.doi.org/10.1371/journal.pone.0215592
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author Buchan, Kyle D.
Prajsnar, Tomasz K.
Ogryzko, Nikolay V.
de Jong, Nienke W. M.
van Gent, Michiel
Kolata, Julia
Foster, Simon J.
van Strijp, Jos A. G.
Renshaw, Stephen A.
author_facet Buchan, Kyle D.
Prajsnar, Tomasz K.
Ogryzko, Nikolay V.
de Jong, Nienke W. M.
van Gent, Michiel
Kolata, Julia
Foster, Simon J.
van Strijp, Jos A. G.
Renshaw, Stephen A.
author_sort Buchan, Kyle D.
collection PubMed
description The neutrophil enzyme myeloperoxidase (MPO) is a major enzyme made by neutrophils to generate antimicrobial and immunomodulatory compounds, notably hypochlorous acid (HOCl), amplifying their capacity for destroying pathogens and regulating inflammation. Despite its roles in innate immunity, the importance of MPO in preventing infection is unclear, as individuals with MPO deficiency are asymptomatic with the exception of an increased risk of candidiasis. Dysregulation of MPO activity is also linked with inflammatory conditions such as atherosclerosis, emphasising a need to understand the roles of the enzyme in greater detail. Consequently, new tools for investigating granular dynamics in vivo can provide useful insights into how MPO localises within neutrophils, aiding understanding of its role in preventing and exacerbating disease. The zebrafish is a powerful model for investigating the immune system in vivo, as it is genetically tractable, and optically transparent. To visualise MPO activity within zebrafish neutrophils, we created a genetic construct that expresses human MPO as a fusion protein with a C-terminal fluorescent tag, driven by the neutrophil-specific promoter lyz. After introducing the construct into the zebrafish genome by Tol2 transgenesis, we established the Tg(lyz:Hsa.MPO-mEmerald,cmlc2:EGFP)sh496 line, and confirmed transgene expression in zebrafish neutrophils. We observed localisation of MPO-mEmerald within a subcellular location resembling neutrophil granules, mirroring MPO in human neutrophils. In Spotless (mpx(NL144)) larvae—which express a non-functional zebrafish myeloperoxidase—the MPO-mEmerald transgene does not disrupt neutrophil migration to sites of infection or inflammation, suggesting that it is a suitable line for the study of neutrophil granule function. We present a new transgenic line that can be used to investigate neutrophil granule dynamics in vivo without disrupting neutrophil behaviour, with potential applications in studying processing and maturation of MPO during development.
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spelling pubmed-64746082019-05-03 A transgenic zebrafish line for in vivo visualisation of neutrophil myeloperoxidase Buchan, Kyle D. Prajsnar, Tomasz K. Ogryzko, Nikolay V. de Jong, Nienke W. M. van Gent, Michiel Kolata, Julia Foster, Simon J. van Strijp, Jos A. G. Renshaw, Stephen A. PLoS One Research Article The neutrophil enzyme myeloperoxidase (MPO) is a major enzyme made by neutrophils to generate antimicrobial and immunomodulatory compounds, notably hypochlorous acid (HOCl), amplifying their capacity for destroying pathogens and regulating inflammation. Despite its roles in innate immunity, the importance of MPO in preventing infection is unclear, as individuals with MPO deficiency are asymptomatic with the exception of an increased risk of candidiasis. Dysregulation of MPO activity is also linked with inflammatory conditions such as atherosclerosis, emphasising a need to understand the roles of the enzyme in greater detail. Consequently, new tools for investigating granular dynamics in vivo can provide useful insights into how MPO localises within neutrophils, aiding understanding of its role in preventing and exacerbating disease. The zebrafish is a powerful model for investigating the immune system in vivo, as it is genetically tractable, and optically transparent. To visualise MPO activity within zebrafish neutrophils, we created a genetic construct that expresses human MPO as a fusion protein with a C-terminal fluorescent tag, driven by the neutrophil-specific promoter lyz. After introducing the construct into the zebrafish genome by Tol2 transgenesis, we established the Tg(lyz:Hsa.MPO-mEmerald,cmlc2:EGFP)sh496 line, and confirmed transgene expression in zebrafish neutrophils. We observed localisation of MPO-mEmerald within a subcellular location resembling neutrophil granules, mirroring MPO in human neutrophils. In Spotless (mpx(NL144)) larvae—which express a non-functional zebrafish myeloperoxidase—the MPO-mEmerald transgene does not disrupt neutrophil migration to sites of infection or inflammation, suggesting that it is a suitable line for the study of neutrophil granule function. We present a new transgenic line that can be used to investigate neutrophil granule dynamics in vivo without disrupting neutrophil behaviour, with potential applications in studying processing and maturation of MPO during development. Public Library of Science 2019-04-19 /pmc/articles/PMC6474608/ /pubmed/31002727 http://dx.doi.org/10.1371/journal.pone.0215592 Text en © 2019 Buchan 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Buchan, Kyle D.
Prajsnar, Tomasz K.
Ogryzko, Nikolay V.
de Jong, Nienke W. M.
van Gent, Michiel
Kolata, Julia
Foster, Simon J.
van Strijp, Jos A. G.
Renshaw, Stephen A.
A transgenic zebrafish line for in vivo visualisation of neutrophil myeloperoxidase
title A transgenic zebrafish line for in vivo visualisation of neutrophil myeloperoxidase
title_full A transgenic zebrafish line for in vivo visualisation of neutrophil myeloperoxidase
title_fullStr A transgenic zebrafish line for in vivo visualisation of neutrophil myeloperoxidase
title_full_unstemmed A transgenic zebrafish line for in vivo visualisation of neutrophil myeloperoxidase
title_short A transgenic zebrafish line for in vivo visualisation of neutrophil myeloperoxidase
title_sort transgenic zebrafish line for in vivo visualisation of neutrophil myeloperoxidase
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474608/
https://www.ncbi.nlm.nih.gov/pubmed/31002727
http://dx.doi.org/10.1371/journal.pone.0215592
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