出版社：American Society for Biochemistry and Molecular Biology
摘要：Microsomal triglyceride transfer protein (MTTP) deficiency results in a syndrome of hypolipidemia and accelerated NAFLD. Animal models of decreased hepatic MTTP activity have revealed an unexplained dissociation between hepatic steatosis and hepatic insulin resistance. Here, we performed comprehensive metabolic phenotyping of liver-specific MTTP knockout (L- Mttp −/− ) mice and age-weight matched wild-type control mice. Young (10–12-week-old) L- Mttp −/− mice exhibited hepatic steatosis and increased DAG content; however, the increase in hepatic DAG content was partitioned to the lipid droplet and was not increased in the plasma membrane. Young L- Mttp −/− mice also manifested normal hepatic insulin sensitivity, as assessed by hyperinsulinemic-euglycemic clamps, no PKCε activation, and normal hepatic insulin signaling from the insulin receptor through AKT Ser/Thr kinase. In contrast, aged (10-month-old) L- Mttp −/− mice exhibited glucose intolerance and hepatic insulin resistance along with an increase in hepatic plasma membrane sn -1,2-DAG content and PKCε activation. Treatment with a functionally liver-targeted mitochondrial uncoupler protected the aged L- Mttp −/− mice against the development of hepatic steatosis, increased plasma membrane sn -1,2-DAG content, PKCε activation, and hepatic insulin resistance. Furthermore, increased hepatic insulin sensitivity in the aged controlled-release mitochondrial protonophore-treated L- Mttp −/− mice was not associated with any reductions in hepatic ceramide content. Taken together, these data demonstrate that differences in the intracellular compartmentation of sn -1,2-DAGs in the lipid droplet versus plasma membrane explains the dissociation of NAFLD/lipid-induced hepatic insulin resistance in young L- Mttp −/− mice as well as the development of lipid-induced hepatic insulin resistance in aged L- Mttp −/− mice.
关键词：lipids ; liver ; metabolic disease ; nonalcoholic fatty liver disease ; drug therapy ; liver microsomal triglyceride transfer protein ; diabetes ; liver-targeted mitochondrial uncoupler
