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Vitamin D3 regulates PM-driven primary human neutrophil inflammatory responses

Recent evidence has demonstrated that both acute and chronic exposure to particulate air pollution are risk factors for respiratory tract infections and increased mortality from sepsis. There is therefore an urgent need to establish the impact of ambient particulate matter (PM) on innate immune cell...

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Autores principales: Kewcharoenwong, Chidchamai, Khongmee, Aranya, Nithichanon, Arnone, Palaga, Tanapat, Prueksasit, Tassanee, Mudway, Ian S., Hawrylowicz, Catherine M., Lertmemongkolchai, Ganjana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516903/
https://www.ncbi.nlm.nih.gov/pubmed/37740033
http://dx.doi.org/10.1038/s41598-023-43252-1
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author Kewcharoenwong, Chidchamai
Khongmee, Aranya
Nithichanon, Arnone
Palaga, Tanapat
Prueksasit, Tassanee
Mudway, Ian S.
Hawrylowicz, Catherine M.
Lertmemongkolchai, Ganjana
author_facet Kewcharoenwong, Chidchamai
Khongmee, Aranya
Nithichanon, Arnone
Palaga, Tanapat
Prueksasit, Tassanee
Mudway, Ian S.
Hawrylowicz, Catherine M.
Lertmemongkolchai, Ganjana
author_sort Kewcharoenwong, Chidchamai
collection PubMed
description Recent evidence has demonstrated that both acute and chronic exposure to particulate air pollution are risk factors for respiratory tract infections and increased mortality from sepsis. There is therefore an urgent need to establish the impact of ambient particulate matter (PM) on innate immune cells and to establish potential strategies to mitigate against adverse effects. PM has previously been reported to have potential adverse effects on neutrophil function. In the present study, we investigated the impact of standard urban PM (SRM1648a, NIST) and PM(2.5) collected from Chiang Mai, Thailand, on human peripheral blood neutrophil functions, including LPS-induced migration, IL-8 production, and bacterial killing. Both NIST and the PM(2.5), being collected in Chiang Mai, Thailand, increased IL-8 production, but reduced CXCR2 expression and migration of human primary neutrophils stimulated with Escherichia coli LPS. Moreover, PM-pretreated neutrophils from vitamin D-insufficient participants showed reduced E. coli-killing activity. Furthermore, in vitro vitamin D3 supplementation attenuated IL-8 production and improved bacterial killing by cells from vitamin D-insufficient participants. Our findings suggest that provision of vitamin D to individuals with insufficiency may attenuate adverse acute neutrophilic responses to ambient PM.
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spelling pubmed-105169032023-09-24 Vitamin D3 regulates PM-driven primary human neutrophil inflammatory responses Kewcharoenwong, Chidchamai Khongmee, Aranya Nithichanon, Arnone Palaga, Tanapat Prueksasit, Tassanee Mudway, Ian S. Hawrylowicz, Catherine M. Lertmemongkolchai, Ganjana Sci Rep Article Recent evidence has demonstrated that both acute and chronic exposure to particulate air pollution are risk factors for respiratory tract infections and increased mortality from sepsis. There is therefore an urgent need to establish the impact of ambient particulate matter (PM) on innate immune cells and to establish potential strategies to mitigate against adverse effects. PM has previously been reported to have potential adverse effects on neutrophil function. In the present study, we investigated the impact of standard urban PM (SRM1648a, NIST) and PM(2.5) collected from Chiang Mai, Thailand, on human peripheral blood neutrophil functions, including LPS-induced migration, IL-8 production, and bacterial killing. Both NIST and the PM(2.5), being collected in Chiang Mai, Thailand, increased IL-8 production, but reduced CXCR2 expression and migration of human primary neutrophils stimulated with Escherichia coli LPS. Moreover, PM-pretreated neutrophils from vitamin D-insufficient participants showed reduced E. coli-killing activity. Furthermore, in vitro vitamin D3 supplementation attenuated IL-8 production and improved bacterial killing by cells from vitamin D-insufficient participants. Our findings suggest that provision of vitamin D to individuals with insufficiency may attenuate adverse acute neutrophilic responses to ambient PM. Nature Publishing Group UK 2023-09-22 /pmc/articles/PMC10516903/ /pubmed/37740033 http://dx.doi.org/10.1038/s41598-023-43252-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kewcharoenwong, Chidchamai
Khongmee, Aranya
Nithichanon, Arnone
Palaga, Tanapat
Prueksasit, Tassanee
Mudway, Ian S.
Hawrylowicz, Catherine M.
Lertmemongkolchai, Ganjana
Vitamin D3 regulates PM-driven primary human neutrophil inflammatory responses
title Vitamin D3 regulates PM-driven primary human neutrophil inflammatory responses
title_full Vitamin D3 regulates PM-driven primary human neutrophil inflammatory responses
title_fullStr Vitamin D3 regulates PM-driven primary human neutrophil inflammatory responses
title_full_unstemmed Vitamin D3 regulates PM-driven primary human neutrophil inflammatory responses
title_short Vitamin D3 regulates PM-driven primary human neutrophil inflammatory responses
title_sort vitamin d3 regulates pm-driven primary human neutrophil inflammatory responses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516903/
https://www.ncbi.nlm.nih.gov/pubmed/37740033
http://dx.doi.org/10.1038/s41598-023-43252-1
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