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Neutrophil Functional Heterogeneity: Identification of Competitive Phagocytosis

INTRODUCTION: Phagocytosis by neutrophils is a key process in the innate immune response against invading microorganisms. Despite reported heterogeneity in other neutrophils functions, little is known regarding differences in phagocytosis by individual cells. Therefore, we tested the hypothesis that...

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Autores principales: Hellebrekers, Pien, Hietbrink, Falco, Vrisekoop, Nienke, Leenen, Luke P. H., Koenderman, Leo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684128/
https://www.ncbi.nlm.nih.gov/pubmed/29170663
http://dx.doi.org/10.3389/fimmu.2017.01498
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author Hellebrekers, Pien
Hietbrink, Falco
Vrisekoop, Nienke
Leenen, Luke P. H.
Koenderman, Leo
author_facet Hellebrekers, Pien
Hietbrink, Falco
Vrisekoop, Nienke
Leenen, Luke P. H.
Koenderman, Leo
author_sort Hellebrekers, Pien
collection PubMed
description INTRODUCTION: Phagocytosis by neutrophils is a key process in the innate immune response against invading microorganisms. Despite reported heterogeneity in other neutrophils functions, little is known regarding differences in phagocytosis by individual cells. Therefore, we tested the hypothesis that heterogeneity is present in the neutrophil compartment in its potency to phagocytize bacteria. METHODS: Phagocytosis assays were performed in suspension with isolated neutrophils and Staphylococcus aureus expressing different fluorescent proteins at MOIs between 1 and 10. Repetitive addition of bacteria with different fluorescent proteins and MOIs was used to compare the phagocytic capacity of S. aureus-green fluorescent protein (GFP)-positive and negative neutrophils and exclude randomness. RESULTS: The percentage and mean fluorescence intensity (MFI) of S. aureus-GFP-positive neutrophils increased with higher MOIs. The increase in MFI was due to phagocytosis of multiple bacteria per neutrophil as was confirmed by confocal imaging. Sequential phagocytosis of GFP- and mCherry-expressing S. aureus showed a non-random process, as S. aureus-GFP-positive neutrophils preferentially phagocytized S. aureus-mCherry. CONCLUSION: All neutrophils were able to phagocytize S. aureus, but some were much more potent than others. Therefore, at physiologically relevant MOIs these potent phagocytizing neutrophils will outcompete the uptake of bacteria by less competent cells in a process we propose to name “competitive phagocytosis.”
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spelling pubmed-56841282017-11-23 Neutrophil Functional Heterogeneity: Identification of Competitive Phagocytosis Hellebrekers, Pien Hietbrink, Falco Vrisekoop, Nienke Leenen, Luke P. H. Koenderman, Leo Front Immunol Immunology INTRODUCTION: Phagocytosis by neutrophils is a key process in the innate immune response against invading microorganisms. Despite reported heterogeneity in other neutrophils functions, little is known regarding differences in phagocytosis by individual cells. Therefore, we tested the hypothesis that heterogeneity is present in the neutrophil compartment in its potency to phagocytize bacteria. METHODS: Phagocytosis assays were performed in suspension with isolated neutrophils and Staphylococcus aureus expressing different fluorescent proteins at MOIs between 1 and 10. Repetitive addition of bacteria with different fluorescent proteins and MOIs was used to compare the phagocytic capacity of S. aureus-green fluorescent protein (GFP)-positive and negative neutrophils and exclude randomness. RESULTS: The percentage and mean fluorescence intensity (MFI) of S. aureus-GFP-positive neutrophils increased with higher MOIs. The increase in MFI was due to phagocytosis of multiple bacteria per neutrophil as was confirmed by confocal imaging. Sequential phagocytosis of GFP- and mCherry-expressing S. aureus showed a non-random process, as S. aureus-GFP-positive neutrophils preferentially phagocytized S. aureus-mCherry. CONCLUSION: All neutrophils were able to phagocytize S. aureus, but some were much more potent than others. Therefore, at physiologically relevant MOIs these potent phagocytizing neutrophils will outcompete the uptake of bacteria by less competent cells in a process we propose to name “competitive phagocytosis.” Frontiers Media S.A. 2017-11-09 /pmc/articles/PMC5684128/ /pubmed/29170663 http://dx.doi.org/10.3389/fimmu.2017.01498 Text en Copyright © 2017 Hellebrekers, Hietbrink, Vrisekoop, Leenen and Koenderman. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Hellebrekers, Pien
Hietbrink, Falco
Vrisekoop, Nienke
Leenen, Luke P. H.
Koenderman, Leo
Neutrophil Functional Heterogeneity: Identification of Competitive Phagocytosis
title Neutrophil Functional Heterogeneity: Identification of Competitive Phagocytosis
title_full Neutrophil Functional Heterogeneity: Identification of Competitive Phagocytosis
title_fullStr Neutrophil Functional Heterogeneity: Identification of Competitive Phagocytosis
title_full_unstemmed Neutrophil Functional Heterogeneity: Identification of Competitive Phagocytosis
title_short Neutrophil Functional Heterogeneity: Identification of Competitive Phagocytosis
title_sort neutrophil functional heterogeneity: identification of competitive phagocytosis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684128/
https://www.ncbi.nlm.nih.gov/pubmed/29170663
http://dx.doi.org/10.3389/fimmu.2017.01498
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