Kupffer cell depletion by CI2MDP-liposomes alters hepatic cytokine expression and delays liver regeneration after partial hepatectomy

Background: Although Kupffer cells (KCs) are capable of producing important growth-stimulating cytokines, their role in liver regeneration following p artial hepatectomy (PH) remains poorly understood. Methods: In the present study liver regeneration was studied after KC-depletion by intravenous admi nistration of liposome-encapsulated dichloromethylene-diphosphonate (Cl2MDP )I a method known to physically eliminate KCs. Furthermore, splenectomy was performed one week prior to PH to exclude the effect of Cl2MDP-liposomes o n macrophage populations in the spleen. Results: KC-depletion was confirmed in cryostat liver sections stained with the monoclonal antibody ED2, a mar ker for resident tissue macrophages. Forty-eight hours after PH, the cumula tive hepatocyte DNA synthesis, as determined in liver sections by the hepat ocyte bromodeoxyuridine labeling index, was significantly decreased in KC-d epleted rats when compared to control-rats. The weight of the remnant liver , expressed as a percentage of the initial liver weight, was significantly less at 96 h after PH in KC-depleted rats. KC-depletion abolished the hepat ic interleukin-6 (IL-6) and interleukin-10 (IL-10) mRNA synthesis and decre ased hepatic expression of tumor necrosis factor-alpha (TNF-alpha), hepatoc yte growth factor (HGF) and transforming growth factor-beta(1) (TGF-beta 1) mRNA after PH, as was assessed by reverse-transcriptase polymerase chain r eaction (RT-PCR). Moreover, at 4 h after PH the systemic release of IL-6 wa s significantly decreased in KC-depleted rats. Conclusion: We conclude that KCs are important for hepatocyte regeneration after PH. Delayed liver rege neration in KC-depleted rats can be explained, at least in part, by an imba lanced hepatic cytokine expression, thereby suppressing important growth-st imulating cytokines.