Development and validation of a novel 3D human in vitro model of nonalcoholic steatohepatitis to be used for novel therapeutic screening and research on disease mechanism.

Period of Performance: 07/18/2017 - 03/31/2018

$222K

Phase 2 SBIR

Recipient Firm

Organovo, Inc.
SAN DIEGO, CA 92121
Principal Investigator

Abstract

ABSTRACT Nonalcoholic fatty liver disease (NAFLD) is a chronic condition that originates as lipid accumulation within hepatocytes (steatosis) and progresses into nonalcoholic steatohepatitis (NASH), characterized by lipid accumulation, inflammation, oxidative stress, and fibrosis. An estimated 100 million adults across the U.S. are thought to have NAFLD, with up to 20 million more estimated to have NASH. Left unchecked, the disease can advance to cirrhosis and hepatocellular carcinoma. Currently, NASH contributes to one third of hepatocellular carcinomas in the US and is the second leading cause of liver transplants in the US. NASH is often referred to as a ?silent? disease as most patients are asymptomatic until problems arise from cirrhosis and liver failure and diagnosis only possible via invasive liver biopsies. Despite well-defined morphological features and decades of intense research worldwide, the mechanisms of NAFLD progression as well as therapeutic approaches and non-invasive diagnostics are still resoundingly absent. Recently, Organovo developed ExVive? Human Liver Tissue, an in vitro 3D bioprinted liver model comprising primary human hepatocytes, hepatic stellates and endothelial cells that better mimics native human liver biology over extended time in culture. The technological advancement of 3D bioprinting enables controlled, reproducible fabrication of 3D liver tissues ex vivo from human cells, yielding a durable liver model with complex composition and architecture that retains metabolic competence and liver-specific functions for at least 4 weeks in culture. The current Fast Track SBIR application seeks to utilize ExVive? Human Liver Tissue to model the onset and progression of human NAFLD via nutrient overload in the first Phase, followed by induction of inflammation, oxidative stress and fibrosis to mimic human NASH in the second Phase. Importantly, in order to drive adoption, the steatosis and NASH models will be validated via comparisons of genomic data with clinically confirmed NAFLD patient data in collaboration with key opinion leader Dr. David Brenner, and verification of altered drug metabolism and disposition via CYP1A2 and 2C9 activities. Lastly, prevention of NAFLD progression and regression of NASH will be assessed via therapeutic modulation of disease phenotypes. Together, these in vitro models have the potential to significantly impact liver disease research by enabling the discovery of novel therapeutics, biomarkers to non-invasively delineate NASH from steatosis, and allow the safety assessment of drugs in a disease relevant background.