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Air pollution aggravates renal ischaemia-reperfusion-induced acute kidney injury.

Authors :
Sanches TR
Parra AC
Sun P
Graner MP
Itto LYU
Butter LM
Claessen N
Roelofs JJ
Florquin S
Veras MM
Andrade MF
Saldiva PHN
Kers J
Andrade L
Tammaro A
Source :
The Journal of pathology [J Pathol] 2024 Aug; Vol. 263 (4-5), pp. 496-507. Date of Electronic Publication: 2024 Jun 27.
Publication Year :
2024

Abstract

Chronic kidney disease (CKD) has emerged as a significant global public health concern. Recent epidemiological studies have highlighted the link between exposure to fine particulate matter (PM <subscript>2.5</subscript> ) and a decline in renal function. PM <subscript>2.5</subscript> exerts harmful effects on various organs through oxidative stress and inflammation. Acute kidney injury (AKI) resulting from ischaemia-reperfusion injury (IRI) involves biological processes similar to those involved in PM <subscript>2.5</subscript> toxicity and is a known risk factor for CKD. The objective of this study was to investigate the impact of PM <subscript>2.5</subscript> exposure on IRI-induced AKI. Through a unique environmentally controlled setup, mice were exposed to urban PM <subscript>2.5</subscript> or filtered air for 12 weeks before IRI followed by euthanasia 48 h after surgery. Animals exposed to PM <subscript>2.5</subscript> and IRI exhibited reduced glomerular filtration, impaired urine concentration ability, and significant tubular damage. Further, PM <subscript>2.5</subscript> aggravated local innate immune responses and mitochondrial dysfunction, as well as enhancing cyclic GMP-AMP synthase-stimulator of interferon genes (cGAS-STING) pathway activation. This increased renal senescence and suppressed the anti-ageing protein klotho, leading to early fibrotic changes. In vitro studies using proximal tubular epithelial cells exposed to PM <subscript>2.5</subscript> and hypoxia/reoxygenation revealed heightened activation of the STING pathway triggered by cytoplasmic mitochondrial DNA, resulting in increased tubular damage and a pro-inflammatory phenotype. In summary, our findings imply a role for PM <subscript>2.5</subscript> in sensitising proximal tubular epithelial cells to IRI-induced damage, suggesting a plausible association between PM <subscript>2.5</subscript> exposure and heightened susceptibility to CKD in individuals experiencing AKI. Strategies aimed at reducing PM <subscript>2.5</subscript> concentrations and implementing preventive measures may improve outcomes for AKI patients and mitigate the progression from AKI to CKD. © 2024 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.<br /> (© 2024 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.)

Details

Language :
English
ISSN :
1096-9896
Volume :
263
Issue :
4-5
Database :
MEDLINE
Journal :
The Journal of pathology
Publication Type :
Academic Journal
Accession number :
38934262
Full Text :
https://doi.org/10.1002/path.6302