The main objective of the Morphology Core is to support the Center Projects' pursuit for the Center's theme with high-quality and specialized morphologic services while achieving the net cost effectiveness. The types of services to be offered are classified into three categories: 1) standard staining of sections following paraffin embedding of tissue s(e.g. hematoxylin and eosin, sinus red for collagen); 2) special immunohistochemistry for frozen sections (e.g. inflammatory cells, cytokines, NF-kappaB); 3) image and morphometric analysis to provide standardized quantitative data. Samples which will be handled by the ore include liver (Research Project 1,2,3) and pancreas (Research Project 4) tissues, primary cultu4res of hepatocytes (Research Project 2), and isolated pancreatic acini (Pilot Project 1). Special staining procedures will be carried out on these samples after preparation of frozen sections, fixation, embedding, cutting, mounting on slides. In the case of cell culture, the cell will be permeabilized and immunostained. Immunofluorescent or immunoperoxidase staining will be performed using specific antibodies against cell constituents, cytokines, chemokines, and NF-kappaB. Quantitation of immunohistochemical staining will be performed by image analysis and/or densitometry. Blinded morphometric analysis for histologic assessment such as fat accumulation, necrosis, fibrosis will also be performed in a standardized fashion. Quality control is maintained at the proposed Core site, Anatomic Pathology Laboratory at Harbor-UCLA Medical Center, which is annually inspected and certified by the College of American Pathology and is under the directorship of the Core Director.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Specialized Center (P50)
Project #
5P50AA011999-04
Application #
6563242
Study Section
Project Start
2002-01-01
Project End
2002-12-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
4
Fiscal Year
2002
Total Cost
$178,517
Indirect Cost
Name
University of Southern California
Department
Type
DUNS #
041544081
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
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
Buxbaum, James; Quezada, Michael; Chong, Bradford et al. (2018) The Pancreatitis Activity Scoring System predicts clinical outcomes in acute pancreatitis: findings from a prospective cohort study. Am J Gastroenterol 113:755-764
Zhao, Qinglan; Wei, Yi; Pandol, Stephen J et al. (2018) STING Signaling Promotes Inflammation in Experimental Acute Pancreatitis. Gastroenterology 154:1822-1835.e2
Edderkaoui, Mouad; Chheda, Chintan; Soufi, Badr et al. (2018) An Inhibitor of GSK3B and HDACs Kills Pancreatic Cancer Cells and Slows Pancreatic Tumor Growth and Metastasis in Mice. Gastroenterology 155:1985-1998.e5
Khanova, Elena; Wu, Raymond; Wang, Wen et al. (2018) Pyroptosis by caspase11/4-gasdermin-D pathway in alcoholic hepatitis in mice and patients. Hepatology 67:1737-1753
Zheng, Han; You, Yang; Hua, Meiyun et al. (2018) Chlorophyllin Modulates Gut Microbiota and Inhibits Intestinal Inflammation to Ameliorate Hepatic Fibrosis in Mice. Front Physiol 9:1671
Lew, Daniel; Wu, Bechien U; Pandol, Stephen J et al. (2018) Disease Course Differences in Acute Pancreatitis Based on Etiology Using the Pancreatitis Activity Scoring System. Pancreas 47:e40-e41
Ogawa, Tomohiro; Li, Yuchang; Lua, Ingrid et al. (2018) Isolation of a unique hepatic stellate cell population expressing integrin ?8 from embryonic mouse livers. Dev Dyn 247:867-881
Tripathi, Anupriya; Debelius, Justine; Brenner, David A et al. (2018) The gut-liver axis and the intersection with the microbiome. Nat Rev Gastroenterol Hepatol 15:397-411
Waldron, Richard T; Su, Hsin-Yuan; Piplani, Honit et al. (2018) Ethanol Induced Disordering of Pancreatic Acinar Cell Endoplasmic Reticulum: An ER Stress/Defective Unfolded Protein Response Model. Cell Mol Gastroenterol Hepatol 5:479-497

Showing the most recent 10 out of 415 publications