Fibrin(ogen) drives repair after acetaminophen-induced liver injury via leukocyte αMβ2 integrin-dependent upregulation of Mmp12

Autor: John E. Froehlich, Nikita Joshi, Holly Cline-Fedewa, Anna V. Wojcicki, Matthew J. Flick, Brendan F. Johnson, Bradley P. Sullivan, Anna K. Kopec, James P. Luyendyk, Jessica L. Ray
Rok vydání: 2017
Předmět:
Zdroj: Journal of Hepatology. 66:787-797
ISSN: 0168-8278
DOI: 10.1016/j.jhep.2016.12.004
Popis: Background & Aims Acetaminophen (APAP)-induced liver injury is coupled with activation of the blood coagulation cascade and fibrin(ogen) accumulation within APAP-injured livers of experimental mice. We sought to define the role of fibrin(ogen) deposition in APAP-induced liver injury and repair. Methods Wild-type, fibrinogen-deficient mice, mutant mice with fibrin(ogen) incapable of binding leukocyte α M β 2 integrin (Fibγ 390-396A mice) and matrix metalloproteinase 12 (Mmp12)-deficient mice were fasted, injected with 300mg/kg APAP i.p. and evaluated at a range of time-points. Plasma and liver tissue were analyzed. Rescue of Fibγ 390-396A mice was carried out with exogenous Mmp12. To examine the effect of the allosteric leukocyte integrin α M β 2 activator leukadherin-1 (LA-1), APAP-treated mice were injected with LA-1. Results In wild-type mice, APAP overdose increased intrahepatic levels of high molecular weight cross-linked fibrin(ogen). Anticoagulation reduced early APAP hepatotoxicity (6h), but increased hepatic injury at 24h, implying a protective role for coagulation at the onset of repair. Complete fibrin(ogen) deficiency delayed liver repair after APAP overdose, evidenced by a reduction of proliferating hepatocytes (24h) and unresolved hepatocellular necrosis (48 and 72h). Fibγ 390-396A mice had decreased hepatocyte proliferation and increased multiple indices of liver injury, suggesting a mechanism related to fibrin(ogen)-leukocyte interaction. Induction of Mmp12, was dramatically reduced in APAP-treated Fibγ 390-396A mice. Mice lacking Mmp12 displayed exacerbated APAP-induced liver injury, resembling Fibγ 390-396A mice. In contrast, administration of LA-1 enhanced hepatic Mmp12 mRNA and reduced necrosis in APAP-treated mice. Further, administration of recombinant Mmp12 protein to APAP-treated Fibγ 390-396A mice restored hepatocyte proliferation. Conclusions These studies highlight a novel pathway of liver repair after APAP overdose, mediated by fibrin(ogen)-α M β 2 integrin engagement, and demonstrate a protective role of Mmp12 expression after APAP overdose. Lay summary Acetaminophen overdose leads to activation of coagulation cascade and deposition of high molecular weight cross-linked fibrin(ogen) species in the liver. Fibrin(ogen) is required for stimulating liver repair after acetaminophen overdose. The mechanism whereby fibrin(ogen) drives liver repair after acetaminophen overdose requires engagement of leukocyte α M β 2 integrin and subsequent induction of matrix metalloproteinase 12.
Databáze: OpenAIRE
Externí odkaz: