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(http://www.niehs.nih.gov//portfolio/index.cfm?do=portfolio.grantdetail&&grant_number=R01ES033898&format=word)
| Principal Investigator: Zacharewski, Timothy R. | |
|---|---|
| Institute Receiving Award | Michigan State University |
| Location | East Lansing, MI |
| Grant Number | R01ES033898 |
| Funding Organization | National Institute of Environmental Health Sciences |
| Award Funding Period | 03 Sep 2022 to 31 Aug 2025 |
| DESCRIPTION (provided by applicant): | Abstract: Non-alcoholic fatty liver disease (NAFLD) describes a spectrum of pathologies which typically involves simple, reversible hepatic fat accumulation (steatosis) progressing into steatohepatitis with fibrosis that increases the risk for more complex metabolic diseases. NAFLD prevalence is projected to increase from ~83 million in 2015 to ~101 million by 2030 in the US alone. Accumulating evidence suggests environmental contaminants play an underappreciated role in NAFLD development and progression. Many chemicals induce fatty liver, but the environmental contaminant, 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), and related compounds, exhibit the greatest potency. Most, if not all, of the effects induced by TCDD are mediated by the aryl hydrocarbon receptor (AHR). We have shown that TCDD induces the progression of steatosis to steatohepatitis (non- alcoholic steatohepatitis (NASH)) with fibrosis, however the underlying mechanisms are poorly understood beyond AHR activation and subsequent changes in gene expression. Our integration of preliminary RNAseq and metabolomics data suggests multiple AHR-mediated effects converge to cause to cause hepatotoxicity and the progression of NAFLD-like pathologies including the repression of hepatic fatty acid oxidation, increased bile acid levels, immune cell infiltration and decreased serum cobalamin (Cbl, aka Vitamin B12) levels. This proposal will test the hypothesis that AHR activation reprograms fatty acid metabolism causing the accumulation of toxic intermediates that contribute to hepatotoxicity and the progression of steatosis to steatohepatitis with fibrosis. In vivo and in vitro genetic and pharmacological approaches will be to further investigate the role of octenoyl-CoA, acrylyl-CoA and dicarboxylic acids (DCAs). Specific Aim 1 will use novel hepatocyte-specific AHR null mice to show that hepatic octenoyl-CoA, acrylyl-CoA and DCAs contribute to hepatotoxicity and NAFLD pathology severity. Specific Aim 2 will use (i) Cbl supplementation to protect against hepatotoxicity and NAFLF progression and (ii) Acod1 null mice to investigate the role of itaconate (Ita) in reducing Cbl levels. Specific Aim 3 will use human HepaRG cells to determine the relevance of AHR-mediated metabolic reprogramming and the accumulation of toxic intermediate metabolites. These results will establish a mechanism that involves AHR-mediated differential gene expression, metabolic reprograming and the biosynthesis of toxic metabolites that contribute to the hepatotoxicity and NAFLD progression. We will show that Cbl supplementation can protect against AHR-mediated hepatotoxicity. Cbl supplementation will also prove to be an effective countermeasure to protect exposed populations susceptible to AHR-mediated hepatotoxicity that may also be beneficial in the treatment and management of NAFLD. |
| Science Code(s)/Area of Science(s) |
Primary: 55 - Liver Secondary: 03 - Carcinogenesis/Cell Transformation |
| Publications | See publications associated with this Grant. |
| Program Officer | Carol Shreffler |