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ABSTRACT: Background
After kidney injury, macrophages transition from initial proinflammatory activation to a proreparative phenotype characterized by expression of arginase-1 (Arg1), mannose receptor 1 (Mrc1), and macrophage scavenger receptor 1 (Msr1). The mechanism by which these alternatively activated macrophages promote repair is unknown.Methods
We characterized the macrophage and renal responses after ischemia-reperfusion injury with contralateral nephrectomy in LysM-Cre;Arg1fl/fl mice and littermate controls and used in vitro coculture of macrophages and tubular cells to determine how macrophage-expressed arginase-1 promotes kidney repair.Results
After ischemia-reperfusion injury with contralateral nephrectomy, Arg1
SUBMITTER: Shin NS
PROVIDER: S-EPMC9161787 | biostudies-literature | 2022 Jun
REPOSITORIES: biostudies-literature