首页|Membrane-bound sn-1,2-diacylglycerols explain the dissociation of hepatic insulin resistance from hepatic steatosis in MTTP knockout mice

Membrane-bound sn-1,2-diacylglycerols explain the dissociation of hepatic insulin resistance from hepatic steatosis in MTTP knockout mice

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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 PKC epsilon 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 PKC epsilon 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, PKC epsilon 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.

lipidslivermetabolic diseasenonalcoholic fatty liver diseasedrug therapyliver microsomal triglyceride transfer proteindiabetesliver-targeted mitochondrial uncoupler

Abulizi, Abudukadier、Vatner, Daniel F.、Ye, Zhang、Wang, Yongliang、Camporez, Joao-Paulo、Zhang, Dongyan、Kahn, Mario、Lyu, Kun、Sirwi, Alaa、Cline, Gary W.、Hussain, M. Mahmood、Aspichueta, Patricia、Samuel, Varman T.、Shulman, Gerald I.

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Yale Sch Med, Dept Internal Med, New Haven, CT 06510 USA

Suny Downstate Med Ctr, Dept Cell Biol, Mineola, NY USA

Univ Basque Country UPV EHU, Fac Med & Nursing, Dept Physiol, Leioa, Spain

2020

Journal of lipid research.

Journal of lipid research.

ISSN:0022-2275
年,卷(期):2020.61(12)
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