The proposed research is directed at defining the cellular and molecular events underlying pathologic fibrosis in the liver. It builds on recent studies that have characterized the specific cell types within the liver that produce extracellular matrix. The data point to hepatic lipocytes (also known as Ito or fat-storing cells) as the major source of extracellular matrix proteins, particularly in liver injury, such as inflammation, where these cells undergo activation with proliferation and increased synthesis of matrix components. Because of their location in the Space of Disse, their impact on the biological function of extracellular matrix in the space of Disse is likely to be important. Of the array of changes exhibited by these cells in fibrosing injury, it is unclear which are central to the altered biologic effects of the pathologic matrix. Proteins that have been assigned cell-binding roles include laminin and fibronectin; thus, changes in their synthesis or conformation within the extracellular matrix could directly affect cell-matrix interaction and the expression of liver-specific functions by hepatocytes. In liver injury, lipocytes may produce variant forms of these proteins. The proposed work will characterize laminin synthesis by lipocytes with specific attention to the presence of putative cell-binding regions in the protein; it will similarly evaluate fibronectin expression, with quantitation of individual isoforms (at the mRNA level) that have been implicated in the injury response of tissues other than liver.
A third aim i s the isolation of laminin receptors from normal rat hepatocytes using a novel affinity matrix in which the biological activity of laminin is preserved. The project will provide the first detailed data on synthesis of laminin and fibronectin by hepatic lipocytes, in both the normal and activated state, in culture and in vivo. By characterizing at a molecular level key events associated with fibrosis, it will contribute importantly to efforts at prophylaxis or therapy for this prevalent and debilitating manifestation of liver disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK031198-11
Application #
3229935
Study Section
General Medicine A Subcommittee 2 (GMA)
Project Start
1982-07-01
Project End
1995-06-30
Budget Start
1992-07-22
Budget End
1993-06-30
Support Year
11
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Wang, Bruce; Dolinski, Brian M; Kikuchi, Noriko et al. (2007) Role of alphavbeta6 integrin in acute biliary fibrosis. Hepatology 46:1404-12
Kikuchi, Shojiro; Griffin, Courtney T; Wang, Shao-Shean et al. (2005) Role of CD44 in epithelial wound repair: migration of rat hepatic stellate cells utilizes hyaluronic acid and CD44v6. J Biol Chem 280:15398-404
Chang, Ming-Ling; Chen, Jeng-Chang; Alonso, Claudio R et al. (2004) Regulation of fibronectin splicing in sinusoidal endothelial cells from normal or injured liver. Proc Natl Acad Sci U S A 101:18093-8
George, J; Wang, S S; Sevcsik, A M et al. (2000) Transforming growth factor-beta initiates wound repair in rat liver through induction of the EIIIA-fibronectin splice isoform. Am J Pathol 156:115-24
Roulot, D; Sevcsik, A M; Coste, T et al. (1999) Role of transforming growth factor beta type II receptor in hepatic fibrosis: studies of human chronic hepatitis C and experimental fibrosis in rats. Hepatology 29:1730-8
George, J; Roulot, D; Koteliansky, V E et al. (1999) In vivo inhibition of rat stellate cell activation by soluble transforming growth factor beta type II receptor: a potential new therapy for hepatic fibrosis. Proc Natl Acad Sci U S A 96:12719-24
McDonagh, A F; Bissell, D M (1998) Porphyria and porphyrinology--the past fifteen years. Semin Liver Dis 18:3-15
Wang, Y J; Wang, S S; Bickel, M et al. (1998) Two novel antifibrotics, HOE 077 and Safironil, modulate stellate cell activation in rat liver injury: differential effects in males and females. Am J Pathol 152:279-87
Racine-Samson, L; Rockey, D C; Bissell, D M (1997) The role of alpha1beta1 integrin in wound contraction. A quantitative analysis of liver myofibroblasts in vivo and in primary culture. J Biol Chem 272:30911-7
Rockey, D C; Chung, J J (1995) Inducible nitric oxide synthase in rat hepatic lipocytes and the effect of nitric oxide on lipocyte contractility. J Clin Invest 95:1199-206

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