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Vitamin D3 regulates PM-driven primary human neutrophil inflammatory responses
Chidchamai Kewcharoenwong1,2, Aranya Khongmee2, Arnone Nithichanon2,3
1Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai, 50200, Thailand.
Scientific Reports
|September 22, 2023
Summary
Particulate matter (PM) air pollution impairs neutrophil function and bacterial killing. Vitamin D supplementation may mitigate these adverse effects in individuals with vitamin D insufficiency.
Area of Science:
- Immunology
- Environmental Health
- Toxicology
Background:
- Particulate matter (PM) air pollution is linked to respiratory infections and sepsis mortality.
- PM exposure may adversely affect neutrophil function, a key component of innate immunity.
- Strategies to mitigate PM's impact on immune cells are urgently needed.
Purpose of the Study:
- To investigate the effects of urban PM and PM2.5 on human neutrophil functions.
- To assess the role of vitamin D in modulating PM-induced neutrophil dysfunction.
- To explore vitamin D supplementation as a potential mitigation strategy.
Main Methods:
- Human peripheral blood neutrophils were exposed to standard urban PM (SRM1648a, NIST) and PM2.5 from Thailand.
- Neutrophil functions assessed included IL-8 production, CXCR2 expression, migration, and bacterial killing.
- Effects were evaluated in both sufficient and insufficient vitamin D states, with in vitro vitamin D3 supplementation.
Main Results:
- Both PM types increased IL-8 production but reduced CXCR2 expression and LPS-induced migration.
- PM-exposed neutrophils from vitamin D-insufficient individuals showed impaired E. coli killing.
- In vitro vitamin D3 supplementation improved bacterial killing and reduced IL-8 production in these cells.
Conclusions:
- Ambient PM exposure negatively impacts human neutrophil function, including migration and bacterial clearance.
- Vitamin D insufficiency exacerbates PM-induced neutrophil dysfunction.
- Vitamin D supplementation shows promise in attenuating adverse neutrophilic responses to PM.
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