
This study validated the use of deceased transplant donor kidneys to model acute kidney injury (AKI) and employed multi-omics and imaging approaches to characterize these kidneys. Consistent changes in injury and inflammatory markers were noted in donors with reduced kidney function. Analyses revealed associations between kidney cells and immune cells, linking them to inflammation. Eight metabolic pathways, including arachidonic acid metabolism, were upregulated with impaired function. Inhibition of cytosolic phospholipase A2 reduced injury and inflammation in vitro, highlighting potential therapeutic targets for AKI.
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