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Neutrophils actively swell to potentiate rapid migration

While the involvement of actin polymerization in membrane protrusion is well-established, we have a more limited understanding of the role of transmembrane water flow in cell motility. Here we investigate the role of water influx in neutrophil migration. These cells undergo directed movement to site...

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Detalles Bibliográficos
Autores principales: Nagy, Tamas L, Strickland, Jack, Weiner, Orion D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245588/
https://www.ncbi.nlm.nih.gov/pubmed/37292824
http://dx.doi.org/10.1101/2023.05.15.540704
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author Nagy, Tamas L
Strickland, Jack
Weiner, Orion D
author_facet Nagy, Tamas L
Strickland, Jack
Weiner, Orion D
author_sort Nagy, Tamas L
collection PubMed
description While the involvement of actin polymerization in membrane protrusion is well-established, we have a more limited understanding of the role of transmembrane water flow in cell motility. Here we investigate the role of water influx in neutrophil migration. These cells undergo directed movement to sites of injury and infection. Chemoattractant exposure increases cell volume and potentiates neutrophil migration, but the causal link between these processes is not known. Using a genome-wide CRISPR screen, we identify the regulators of the chemoattractant-induced neutrophil swelling, including NHE1, AE2, PI3K-gamma, and CA2. Through NHE1 inhibition in primary human neutrophils, we show that cell swelling is both necessary and sufficient for rapid migration following chemoattractant stimulation. Our data demonstrate that cell swelling complements cytoskeletal inputs for chemoattractant-induced potentiation of migration.
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spelling pubmed-102455882023-06-08 Neutrophils actively swell to potentiate rapid migration Nagy, Tamas L Strickland, Jack Weiner, Orion D bioRxiv Article While the involvement of actin polymerization in membrane protrusion is well-established, we have a more limited understanding of the role of transmembrane water flow in cell motility. Here we investigate the role of water influx in neutrophil migration. These cells undergo directed movement to sites of injury and infection. Chemoattractant exposure increases cell volume and potentiates neutrophil migration, but the causal link between these processes is not known. Using a genome-wide CRISPR screen, we identify the regulators of the chemoattractant-induced neutrophil swelling, including NHE1, AE2, PI3K-gamma, and CA2. Through NHE1 inhibition in primary human neutrophils, we show that cell swelling is both necessary and sufficient for rapid migration following chemoattractant stimulation. Our data demonstrate that cell swelling complements cytoskeletal inputs for chemoattractant-induced potentiation of migration. Cold Spring Harbor Laboratory 2023-07-05 /pmc/articles/PMC10245588/ /pubmed/37292824 http://dx.doi.org/10.1101/2023.05.15.540704 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Nagy, Tamas L
Strickland, Jack
Weiner, Orion D
Neutrophils actively swell to potentiate rapid migration
title Neutrophils actively swell to potentiate rapid migration
title_full Neutrophils actively swell to potentiate rapid migration
title_fullStr Neutrophils actively swell to potentiate rapid migration
title_full_unstemmed Neutrophils actively swell to potentiate rapid migration
title_short Neutrophils actively swell to potentiate rapid migration
title_sort neutrophils actively swell to potentiate rapid migration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245588/
https://www.ncbi.nlm.nih.gov/pubmed/37292824
http://dx.doi.org/10.1101/2023.05.15.540704
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