Publication Date

12-2019

Date of Final Oral Examination (Defense)

12-2-2019

Type of Culminating Activity

Dissertation

Degree Title

Doctor of Philosophy in Biomolecular Sciences

Department

Biology

Supervisory Committee Chair

Kristen A. Mitchell, Ph.D.

Supervisory Committee Member

Kenneth A. Cornell, Ph.D.

Supervisory Committee Member

Allan R. Albig, Ph.D.

Supervisory Committee Member

Daniel Fologea, Ph.D.

Supervisory Committee Member

Denise G. Wingett, Ph.D.

Abstract

Liver disease is a worldwide problem and the 9th leading cause of death in the United States. Common causes of liver disease include alcohol abuse, virus infection, and nonalcoholic fatty liver. Regardless of etiology, liver damage elicits inflammation and drives the activation of hepatic stellate cells (HSCs), which deposit collagen throughout the liver. During chronic injury, excessive collagen deposition, referred to as fibrosis or “scarring”, can progress to cirrhosis, cancer, and organ failure. Emerging evidence indicates a strong association between liver disease and exposure to environmental chemicals. This research investigated mechanisms by which exposure to the environmental contaminant 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) impacts liver disease. TCDD is representative of a family of chemicals that elicit toxicity through the aryl hydrocarbon receptor (AhR). A mouse model system was used in which liver damage was first induced with carbon tetrachloride, and TCDD was administered as a “second hit.” We used mice with the AhR selectively removed from either HSCs or hepatocytes. Results indicate that TCDD treatment exacerbated injury, inflammation and HSC activation through a mechanism that required AhR signaling in hepatocytes. Furthermore, TCDD treatment produced changes in gene expression consistent with a condition called non-alcoholic fatty liver disease. The results raise the intriguing possibility that exposure to environmental contaminants may facilitate liver disease progression in an already-injured liver.

DOI

10.18122/td/1632/boisestate

Included in

Toxicology Commons

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