Air pollution aggravates renal ischaemia–reperfusion‐induced acute kidney injury

Author:

Sanches Talita Rojas1ORCID,Parra Antonio Carlos1ORCID,Sun Peiqi2ORCID,Graner Mariana Pereira1ORCID,Itto Lucas Yuji Umesaki1ORCID,Butter Loes Maria2,Claessen Nike2,Roelofs Joris JTH23ORCID,Florquin Sandrine23ORCID,Veras Mariana Matera4ORCID,Andrade Maria de Fatima5ORCID,Saldiva Paulo Hilário Nascimento236ORCID,Kers Jesper236ORCID,Andrade Lucia1ORCID,Tammaro Alessandra2ORCID

Affiliation:

1. Laboratory of Basic Science in Renal Diseases (LIM‐12), Division of Nephrology School of Medicine, University of São Paulo São Paulo Brazil

2. Department of Pathology, Amsterdam Cardiovascular Science and Amsterdam Infection and Immunity Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands

3. Department of Pathology Leiden University Medical Centre Leiden The Netherlands

4. Laboratory of Environmental and Experimental Pathology (LIM‐5), Department of Pathology School of Medicine, University of São Paulo São Paulo Brazil

5. Institute of Astronomy, Geophysics and Atmospheric Sciences (IAG) University of São Paulo São Paulo Brazil

6. Biomolecular Systems Analytics, Van't Hoff Institute for Molecular Sciences (HIMS) University of Amsterdam Amsterdam The Netherlands

Abstract

AbstractChronic 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 (PM2.5) and a decline in renal function. PM2.5 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 PM2.5 toxicity and is a known risk factor for CKD. The objective of this study was to investigate the impact of PM2.5 exposure on IRI‐induced AKI. Through a unique environmentally controlled setup, mice were exposed to urban PM2.5 or filtered air for 12 weeks before IRI followed by euthanasia 48 h after surgery. Animals exposed to PM2.5 and IRI exhibited reduced glomerular filtration, impaired urine concentration ability, and significant tubular damage. Further, PM2.5 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 PM2.5 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 PM2.5 in sensitising proximal tubular epithelial cells to IRI‐induced damage, suggesting a plausible association between PM2.5 exposure and heightened susceptibility to CKD in individuals experiencing AKI. Strategies aimed at reducing PM2.5 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.

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Conselho Nacional de Desenvolvimento Científico e Tecnológico

ZonMw

Publisher

Wiley

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