This proposal will study the specific subpopulations of cells in the liver that are involved during the regeneration of damaged and diseased liver. A mouse model of the human hereditary disease tyrosinemia type I (HTI) will be used, this disease is characteristic of several inherited metabolic diseases in which one gene is absent. HTI is due to the loss of the enzyme fumarylacetoacetate hydrolase (FAH) resulting in progressive liver damage and a high frequency of hepatocellular cancer. It has been discovered that hepatocytes that express this enzyme possess a selective growth advantage over cells that do not express FAH in the liver. Isolation and transplantation of specific subpopulations of FAH expressing cells into the livers of FAH deficient mice should allow for the identification of specific liver cell subpopulations which are involved in liver regeneration. This proposal also studies the use of retroviral gene therapy by transducing cells in FAH deficient mice with a FAH expressing retrovirus and studying their selective growth advantage. These experiments, determining the regenerative subpopulation of liver cells and treatment of FAH deficient mice with retroviral gene therapy, could prove valuable in designing a treatment for human tyrosinemia and other liver and related metabolic diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32DK009429-03
Application #
2684049
Study Section
Medical Biochemistry Study Section (MEDB)
Program Officer
Hyde, James F
Project Start
1998-04-01
Project End
Budget Start
1998-04-01
Budget End
1998-09-30
Support Year
3
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Oregon Health and Science University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
009584210
City
Portland
State
OR
Country
United States
Zip Code
97239
Overturf, K; Al-Dhalimy, M; Finegold, M et al. (1999) The repopulation potential of hepatocyte populations differing in size and prior mitotic expansion. Am J Pathol 155:2135-43
Overturf, K; Al-Dhalimy, M; Manning, K et al. (1998) Ex vivo hepatic gene therapy of a mouse model of Hereditary Tyrosinemia Type I. Hum Gene Ther 9:295-304
Grompe, M; Overturf, K; al-Dhalimy, M et al. (1998) Therapeutic trials in the murine model of hereditary tyrosinaemia type I: a progress report. J Inherit Metab Dis 21:518-31
Overturf, K; al-Dhalimy, M; Ou, C N et al. (1997) Serial transplantation reveals the stem-cell-like regenerative potential of adult mouse hepatocytes. Am J Pathol 151:1273-80