Role of ATG14 in the regulation of hepatic function

NIH RePORTER · NIH · R01 · $441,299 · view on reporter.nih.gov ↗

Abstract

Project Summary Nonalcoholic fatty liver disease (NAFLD) affects over 30% adults in the US. The NAFLD initially manifests as hepatic steatosis and progresses to nonalcoholic steatohepatitis (NASH), fibrosis, and even cirrhosis or hepatocellular carcinoma. Due to the progressive nature of the disease, it is crucial to understand the early pathogenic events of the NAFLD development. Among those early events, abnormal lipid metabolism is largely responsible for the hepatic steatosis that is manifested as extra triglyceride accumulation in the liver in the form of lipid droplets. Triglyceride homeostasis is a very dynamic process as it involves both biosynthesis and breakdown. The lipid droplet mobilization remains poorly understood. In this application, the research team will investigate the regulatory mechanisms of lipid droplet breakdown in cellular and animal models with a focus on a key autophagy regulator – autophagy related 14. It is expected that the proposed research will provide key mechanistic insights into the strategy for therapeutic intervention and treatment of NAFLD.

Key facts

NIH application ID
10143232
Project number
5R01DK120689-02
Recipient
INDIANA UNIVERSITY INDIANAPOLIS
Principal Investigator
X. Charlie Dong
Activity code
R01
Funding institute
NIH
Fiscal year
2021
Award amount
$441,299
Award type
5
Project period
2020-06-01 → 2024-03-31