(Taken from the application) The University of Southern California Research Center for Liver Diseases, funded since 1995, has the goal of fostering and facilitating inter-disciplinary research in liver and digestive diseases. The center has 34 members and 13 affiliated members. The Biomedical Research Base consists of four major themes supported by 45 peer-reviewed grants totaling $6.5 million in annual direct costs. These themes include: a) viral hepatitis and liver cancer; b) liver injury: hepatotoxicity, inflammation, fibrosis; c) cell biology and transport; and d) metabolism, signal transduction and gene expression. Four core facilities support this research base: 1) Administrative Core which oversees the operations and budget of the center; the Center Director, Associate Director, Administrator and External Advisory Board oversee the utilization of the cores, the pilot/feasibility program, the Named New Investigator Award, and the enrichment program (seminar series and annual symposium); a Mathematical Analysis Modeling Subcore is available to center members through the Administrative Core; 2) Molecular Biology Core, composed of three major activities (supporting research in gene expression, techniques and equipment) and a Viral Vector Subcore to enhance gene delivery research; 3) Cell Biology Core divided into a Subcellular Organelle Core which provides membrane fractionation, highly enriched sinusoidal and canalicular plasma membrane vesicles, mitochondria and isolated perfused liver, and a Confocal Microscope Subcore for imaging of live and fixed cells; 4) Cell Culture Core divided into Parenchymal Subcore which provides isolated and primary cultured rat, mouse and human hepatocytes and various cell lines, and a Nonparenchymal Subcore which provides isolated and cultured Kupffer cells, hepatic stellate cells and sinusoidal endothelial cells. The center supports Pilot and Feasibility projects in diverse areas related to the themes of the Research Base. Current projects supported by the center include targeting gene therapy to the liver, abnormal liver development in retinoic acid receptor defective mice, the identification and characterization of nitric oxide synthase in liver mitochondria, and the identification of mutations in the epoxide hydrolase gene in human subjects with impaired hepatic uptake of bile acids. The USC Research Center for Liver Diseases is dedicated to attracting and promoting research aimed at understanding, preventing, and treating liver and digestive diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK048522-06
Application #
2901656
Study Section
Special Emphasis Panel (ZDK1-GRB-7 (M1))
Program Officer
Podskalny, Judith M,
Project Start
1995-03-01
Project End
2005-02-28
Budget Start
2000-05-15
Budget End
2001-02-28
Support Year
6
Fiscal Year
2000
Total Cost
$850,001
Indirect Cost
Name
University of Southern California
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
041544081
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
Chang, Huiyi H; Yeh, Jih-Chao; Ichiyama, Ronaldo M et al. (2018) Mapping and neuromodulation of lower urinary tract function using spinal cord stimulation in female rats. Exp Neurol 305:26-32
Chen, Chien-Yu; Chen, Jingyu; He, Lina et al. (2018) PTEN: Tumor Suppressor and Metabolic Regulator. Front Endocrinol (Lausanne) 9:338
Nakamura, Brooke N; Glazier, Alison; Kattah, Michael G et al. (2018) A20 regulates canonical wnt-signaling through an interaction with RIPK4. PLoS One 13:e0195893
Guo, Hao; Lee, Changrim; Shah, Mihir et al. (2018) A novel elastin-like polypeptide drug carrier for cyclosporine A improves tear flow in a mouse model of Sjögren's syndrome. J Control Release 292:183-195
Wu, Raymond; Murali, Ramachandran; Kabe, Yasuaki et al. (2018) Baicalein Targets GTPase-Mediated Autophagy to Eliminate Liver Tumor-Initiating Stem Cell-Like Cells Resistant to mTORC1 Inhibition. Hepatology 68:1726-1740
Ogasawara, Noriko; Poposki, Julie A; Klingler, Aiko I et al. (2018) IL-10, TGF-?, and glucocorticoid prevent the production of type 2 cytokines in human group 2 innate lymphoid cells. J Allergy Clin Immunol 141:1147-1151.e8
Edman, Maria C; Janga, Srikanth R; Meng, Zhen et al. (2018) Increased Cathepsin S activity associated with decreased protease inhibitory capacity contributes to altered tear proteins in Sjögren's Syndrome patients. Sci Rep 8:11044
Baulies, Anna; Montero, Joan; Matías, Nuria et al. (2018) The 2-oxoglutarate carrier promotes liver cancer by sustaining mitochondrial GSH despite cholesterol loading. Redox Biol 14:164-177
Ju, Yaping; Janga, Srikanth Reddy; Klinngam, Wannita et al. (2018) NOD and NOR mice exhibit comparable development of lacrimal gland secretory dysfunction but NOD mice have more severe autoimmune dacryoadenitis. Exp Eye Res 176:243-251
Peddi, Santosh; Pan, Xiaoli; MacKay, John Andrew (2018) Intracellular Delivery of Rapamycin From FKBP Elastin-Like Polypeptides Is Consistent With Macropinocytosis. Front Pharmacol 9:1184

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