Kuroda Yu, Ito Yoshiya, Nishizawa Nobuyuki, Tanabe Mina, Yamashita Atsushi, Hosono Kanako, Kamata Mariko, Satoh Masashi, Kumamoto Yusuke, Hiki Naoki, Amano Hideki
Department of Molecular Pharmacology, Graduate School of Medical Sciences, Kitasato University, Sagamihara, Japan; Department of Pharmacology, Kitasato University School of Medicine, Sagamihara, Japan; Department of Upper Gastrointestinal Surgery, Kitasato University School of Medicine, Sagamihara, Japan.
Department of Molecular Pharmacology, Graduate School of Medical Sciences, Kitasato University, Sagamihara, Japan; Department of Pharmacology, Kitasato University School of Medicine, Sagamihara, Japan.
Exp Cell Res. 2025 Aug 15;451(2):114728. doi: 10.1016/j.yexcr.2025.114728. Epub 2025 Aug 26.
Liver ischemia-reperfusion (IR) injury is a substantial form of damage that occurs during liver transplantation and resection surgeries. Steatotic livers are particularly susceptible to IR injury, but few strategies to effectively alleviate this issue in steatotic livers exist. Invariant natural killer T (iNKT) cells regulate IR injury in healthy livers as well as liver repair by interacting with macrophages. In this study, we explored the role of iNKT cell-macrophage crosstalk in IR injury in steatotic livers. High-fat diet (HFD)-fed macrophage-specific CD1d conditional knockout (Cd1d) and Cd1d control (Cont) mice were subjected to liver IR. HFD-fed CD1d mice showed mitigation of IR-induced liver damages with reduction of hepatic necrosis and inflammation along with promotion of liver repair. Flow cytometric analysis revealed that HFD-fed Cd1d mice showed increased hepatic reparative macrophages and interleukin (IL)-13-positive iNKT cells but decreased pro-inflammatory macrophages with IL-1β. IL-13 administration to HFD-fed Cont mice attenuated IR injury and accelerated liver recovery, which was associated with accumulation of hepatic macrophages skewed to a reparative phenotype. IL-13 promoted reparative macrophage polarization in bone marrow (BM)-derived Cd1d-deficient macrophages in vitro. Blockade of IL-13 in HFD-fed Cd1d mice aggravated IR injury. Overall, inhibiting iNKT cell-macrophage crosstalk attenuates steatotic liver IR injury and facilitates liver repair via IL-13-mediated reparative macrophage polarization. These findings provide new insights into therapeutic strategies to regulate the vulnerability of the steatotic liver to IR injury.
