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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2021-04-01
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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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