Mcl-1 induction, which is a Bcl-2 family member and was regulated by AKT in hepatocytes (Supporting Fig. 6C,E),21 was diminished in Kupffer cell-depleted mice or ASMase−/− bone marrow-transplanted mice, whereas Bcl-XL or Bfl-1 were not affected. These results suggest that survival may be mediated by Mcl-1 at the downstream of AKT. The present study specifically addressed the role of Kupffer cells and of ASMase in the cholestatic liver injury. Our results demonstrate that depletion of Kupffer cells increased liver injury and susceptibility to TNF-α-induced hepatocyte apoptosis, and decreased hepatocyte regeneration and liver fibrosis with reduced AKT activation. Kupffer cell-derived ASMase
was crucial for the AKT activation. The results raise novel therapeutic possibilities for treating liver injury. After BDL, hepatocytes are exposed to elevated concentrations of bile acid, and hydrophobic selleck chemicals llc bile acids lead to hepatocyte cell death22 through various factors such as reactive oxygen species (ROS) generation from mitochondria23 and activation of Fas signaling in a ligand-independent manner by altering cellular trafficking of Fas.24 Indeed, expression of 4-hydroxy-2-nonenal (HNE), which is produced by
lipid peroxidation, was increased on 1 day after the surgery of BDL (data not shown). Because Kupffer cell depletion did not increase the initial liver damage by BDL (1 day after the surgery), it is likely that this damage is induced by a direct see more toxic effect of bile acid rather than subsequent immune responses because Kupffer cells are not activated in this early stage. The initial hepatocyte cell death stimulates subsequent inflammatory responses leading to further liver injury and fibrosis.25, 26 In BDL liver, the engulfment of apoptotic or necrotic body in Kupffer cells is observed,27 which leads to production of cytokines including TNF-α and TGF-β.9 Either a promotive9 or protective10 effect of Kupffer cells on BDL-induced liver injury have been reported. In the 上海皓元 present study, alendronate treatment, which depleted Kupffer cells in the livers, increased liver injury and reduced fibrosis 10 days after BDL, suggesting that Kupffer cells have a protective
effect on the subsequent damage of hepatocytes and a promotive effect on fibrosis in the late stage. The increase of liver injury is probably explained by the diminished Kupffer cell functions, including the phagocytosis of injured tissue and the production of protective factors for hepatocytes. The reduced fibrosis is most likely due to decreased fibrogenic cytokines from Kupffer cells. Cytokines including TGF-β and TGF-α are released from Kupffer cells,28 and HSCs are stimulated to induce collagen I α1 transcription by TGF-β.29 In the liver chronically injured by BDL, hepatocytes represented the survival and regenerative properties, and AKT was a critical factor for the survival and regeneration of the remaining viable hepatocytes.
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