Heme Oxygenase-1 Regulates Myeloid Cell Trafficking in AKI
2015
Renal ischemia-reperfusion injury is mediated by a complex cascade of events, including the immune response, that occur secondary to injury to renal epithelial cells. We tested the hypothesis that heme oxygenase-1 (HO-1) expression, which is protective in ischemia-reperfusion injury, regulates trafficking of myeloid-derived immune cells in the kidney. Age-matched male wild-type (HO-1 +/+ ), HO-1–knockout (HO-1 −/− ), and humanized HO-1–overexpressing (HBAC) mice underwent bilateral renal ischemia for 10 minutes. Ischemia-reperfusion injury resulted in significantly worse renal structure and function and increased mortality in HO-1 −/− mice. In addition, there were more macrophages (CD45 + CD11b hi F4/80 lo ) and neutrophils (CD45 + CD11b hi MHCII − Gr-1 hi ) in HO-1 −/− kidneys than in sham and HO-1 +/+ control kidneys subjected to ischemia-reperfusion. However, ischemic injury resulted in a significant decrease in the intrarenal resident dendritic cell (DC; CD45 + MHCII + CD11b lo F4/80 hi ) population in HO-1 −/− kidneys compared with controls. Syngeneic transplant experiments utilizing green fluorescent protein–positive HO-1 +/+ or HO-1 −/− donor kidneys and green fluorescent protein–negative HO-1 +/+ recipients confirmed increased migration of the resident DC population from HO-1 −/− donor kidneys, compared to HO-1 +/+ donor kidneys, to the peripheral lymphoid organs. This effect on renal DC migration was corroborated in myeloid-specific HO-1 −/− mice subjected to bilateral ischemia. These mice also displayed impaired renal recovery and increased fibrosis at day 7 after injury. These results highlight an important role for HO-1 in orchestrating the trafficking of myeloid cells in AKI, which may represent a key pathway for therapeutic intervention.
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