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Air pollution aggravates renal ischaemia-reperfusion-induced acute kidney injury.
- 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.)
- Subjects :
- Animals
Mice
Male
Air Pollution adverse effects
Disease Models, Animal
Kidney pathology
Kidney metabolism
Signal Transduction
Glomerular Filtration Rate
Acute Kidney Injury pathology
Acute Kidney Injury chemically induced
Acute Kidney Injury etiology
Acute Kidney Injury metabolism
Reperfusion Injury pathology
Particulate Matter adverse effects
Particulate Matter toxicity
Mice, Inbred C57BL
Subjects
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