Liver-specific Prkn knockout mice are more susceptible to diet-induced hepatic steatosis and insulin resistance.

ABSTRACT:

Objective

PARKIN is an E3 ubiquitin ligase that regulates mitochondrial quality control through a process called mitophagy. Recent human and rodent studies suggest that loss of hepatic mitophagy may occur during the pathogenesis of obesity-associated fatty liver and contribute to changes in mitochondrial metabolism associated with this disease. Whole-body Prkn knockout mice are paradoxically protected against diet-induced hepatic steatosis; however, liver-specific effects of Prkn deficiency cannot be discerned in this model due to pleotropic effects of germline Prkn deletion on energy balance and subsequent protection against diet-induced obesity. We therefore generated the first liver-specific Prkn knockout mouse strain (LKO) to directly address the role of hepatic Prkn.

Method

SUBMITTER: Edmunds LR 

PROVIDER: S-EPMC7399260 | biostudies-literature | 2020 Nov

REPOSITORIES: biostudies-literature