TRPM2 ion channels steer neutrophils towards a source of hydrogen peroxide

Abstract Neutrophils must navigate accurately towards pathogens in order to destroy invaders and thus defend our bodies against infection. Here we show that hydrogen peroxide, a potent neutrophil chemoattractant, guides chemotaxis by activating calcium-permeable TRPM2 ion channels and generating an...

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Main Authors: Hassan Morad, Suaib Luqman, Chun-Hsiang Tan, Victoria Swann, Peter A. McNaughton
Format: Article
Language:English
Published: Nature Publishing Group 2021-04-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-88224-5
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spelling doaj-30cdafce157949a5a2be906a5b87c6f52021-05-02T11:31:23ZengNature Publishing GroupScientific Reports2045-23222021-04-0111111610.1038/s41598-021-88224-5TRPM2 ion channels steer neutrophils towards a source of hydrogen peroxideHassan Morad0Suaib Luqman1Chun-Hsiang Tan2Victoria Swann3Peter A. McNaughton4Wolfson Centre for Age-Related Diseases, King’s College LondonWolfson Centre for Age-Related Diseases, King’s College LondonWolfson Centre for Age-Related Diseases, King’s College LondonWolfson Centre for Age-Related Diseases, King’s College LondonWolfson Centre for Age-Related Diseases, King’s College LondonAbstract Neutrophils must navigate accurately towards pathogens in order to destroy invaders and thus defend our bodies against infection. Here we show that hydrogen peroxide, a potent neutrophil chemoattractant, guides chemotaxis by activating calcium-permeable TRPM2 ion channels and generating an intracellular leading-edge calcium “pulse”. The thermal sensitivity of TRPM2 activation means that chemotaxis towards hydrogen peroxide is strongly promoted by small temperature elevations, suggesting that an important function of fever may be to enhance neutrophil chemotaxis by facilitating calcium influx through TRPM2. Chemotaxis towards conventional chemoattractants such as LPS, CXCL2 and C5a does not depend on TRPM2 but is driven in a similar way by leading-edge calcium pulses. Other proposed initiators of neutrophil movement, such as PI3K, Rac and lyn, influence chemotaxis by modulating the amplitude of calcium pulses. We propose that intracellular leading-edge calcium pulses are universal drivers of the motile machinery involved in neutrophil chemotaxis.https://doi.org/10.1038/s41598-021-88224-5
collection DOAJ
language English
format Article
sources DOAJ
author Hassan Morad
Suaib Luqman
Chun-Hsiang Tan
Victoria Swann
Peter A. McNaughton
spellingShingle Hassan Morad
Suaib Luqman
Chun-Hsiang Tan
Victoria Swann
Peter A. McNaughton
TRPM2 ion channels steer neutrophils towards a source of hydrogen peroxide
Scientific Reports
author_facet Hassan Morad
Suaib Luqman
Chun-Hsiang Tan
Victoria Swann
Peter A. McNaughton
author_sort Hassan Morad
title TRPM2 ion channels steer neutrophils towards a source of hydrogen peroxide
title_short TRPM2 ion channels steer neutrophils towards a source of hydrogen peroxide
title_full TRPM2 ion channels steer neutrophils towards a source of hydrogen peroxide
title_fullStr TRPM2 ion channels steer neutrophils towards a source of hydrogen peroxide
title_full_unstemmed TRPM2 ion channels steer neutrophils towards a source of hydrogen peroxide
title_sort trpm2 ion channels steer neutrophils towards a source of hydrogen peroxide
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-04-01
description Abstract Neutrophils must navigate accurately towards pathogens in order to destroy invaders and thus defend our bodies against infection. Here we show that hydrogen peroxide, a potent neutrophil chemoattractant, guides chemotaxis by activating calcium-permeable TRPM2 ion channels and generating an intracellular leading-edge calcium “pulse”. The thermal sensitivity of TRPM2 activation means that chemotaxis towards hydrogen peroxide is strongly promoted by small temperature elevations, suggesting that an important function of fever may be to enhance neutrophil chemotaxis by facilitating calcium influx through TRPM2. Chemotaxis towards conventional chemoattractants such as LPS, CXCL2 and C5a does not depend on TRPM2 but is driven in a similar way by leading-edge calcium pulses. Other proposed initiators of neutrophil movement, such as PI3K, Rac and lyn, influence chemotaxis by modulating the amplitude of calcium pulses. We propose that intracellular leading-edge calcium pulses are universal drivers of the motile machinery involved in neutrophil chemotaxis.
url https://doi.org/10.1038/s41598-021-88224-5
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AT victoriaswann trpm2ionchannelssteerneutrophilstowardsasourceofhydrogenperoxide
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