The Liver-Intestinal Lipid Program Project (LILPP) consists of a group of closely related research projects all dealing with studies of bile acids, cholesterol, phospholipid and triglyceride metabolism and transport by the liver or intestines. The proposed program project consists of seven individual grant applications by independent investigators, with long standing interests in the metabolism of sterols, bile acids and/or other lipids. Four members of the program project are from the Division of Gastroenterology and the other four are from the School of Basic Health Sciences. The overall objective of the program project is to pool the resources and talents of individual investigators in order to further our understanding of hepatic and intestinal metabolism of lipids. The specific objectives of this proposal are to: a) elucidate the mechanisms of regulation of bile acid synthesis and secretion; b) determine the factors which regulate the size of """"""""metabolically active pool"""""""" of free cholesterol in the liver, which is the precursor source for bile acid synthesis and biliary cholesterol excretion; c) to provide a kinetic definition of the contribution of plasma free and esterified cholesterol from different lipoprotein fractions to bile acid synthesis and biliary cholesterol secretion in man (normal subjects and patients with different types of hyperlipidemia); d) to describe the mechanism of regulation of phospholipid and triglyceride synthesis in the liver; e) describe the role of hormones in the regulation of bile salt transport and secretion in the liver; f) to determine the role of bile salt in the intestinal absorption of Ca++ and Fe++ and effects of Ca++ on ileal bile salt absorption and g) to carry outbasic studies of intestinal microbial metabolism of bile acids. The Cell Culture-Molecular Biology Core laboratory, under the direction of Dr. Hylemon, will play a pivotal role in this program project. This core laboratory will offer modern technology not available to several investigators. This aspect of the LILPP will permit a number of P.I.'s a more indepth approach in their studies. Extensive collaborative studies between different investigators have already been initiated and a number of others are in planning phase.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Program Projects (P01)
Project #
5P01DK038030-04
Application #
3095436
Study Section
Special Emphasis Panel (ADDK)
Project Start
1986-12-01
Project End
1991-11-30
Budget Start
1989-12-01
Budget End
1990-11-30
Support Year
4
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Virginia Commonwealth University
Department
Type
Schools of Medicine
DUNS #
City
Richmond
State
VA
Country
United States
Zip Code
23298
Ridlon, Jason M; Hylemon, Phillip B (2012) Identification and characterization of two bile acid coenzyme A transferases from Clostridium scindens, a bile acid 7?-dehydroxylating intestinal bacterium. J Lipid Res 53:66-76
Zhou, Huiping (2011) HIV protease inhibitors induce endoplasmic reticulum stress and disrupt barrier integrity in intestinal epithelial cells. Methods Enzymol 490:107-19
Zha, Weibin; Liang, Guang; Xiao, Jian et al. (2010) Berberine inhibits HIV protease inhibitor-induced inflammatory response by modulating ER stress signaling pathways in murine macrophages. PLoS One 5:e9069
Wu, Xudong; Sun, Lixin; Zha, Weibin et al. (2010) HIV protease inhibitors induce endoplasmic reticulum stress and disrupt barrier integrity in intestinal epithelial cells. Gastroenterology 138:197-209
Ridlon, Jason M; Kang, Dae-Joong; Hylemon, Phillip B (2010) Isolation and characterization of a bile acid inducible 7alpha-dehydroxylating operon in Clostridium hylemonae TN271. Anaerobe 16:137-46
Chen, Li; Jarujaron, Sirikalaya; Wu, Xudong et al. (2009) HIV protease inhibitor lopinavir-induced TNF-alpha and IL-6 expression is coupled to the unfolded protein response and ERK signaling pathways in macrophages. Biochem Pharmacol 78:70-7
Rodriguez-Agudo, Daniel; Ren, Shunlin; Wong, Eric et al. (2008) Intracellular cholesterol transporter StarD4 binds free cholesterol and increases cholesteryl ester formation. J Lipid Res 49:1409-19
Wu, Xudong; Zhang, Luyong; Gurley, Emily et al. (2008) Prevention of free fatty acid-induced hepatic lipotoxicity by 18beta-glycyrrhetinic acid through lysosomal and mitochondrial pathways. Hepatology 47:1905-15
Kang, Dae-Joong; Ridlon, Jason M; Moore 2nd, Doyle Ray et al. (2008) Clostridium scindens baiCD and baiH genes encode stereo-specific 7alpha/7beta-hydroxy-3-oxo-delta4-cholenoic acid oxidoreductases. Biochim Biophys Acta 1781:16-25
Ren, Shunlin; Li, Xiaobo; Rodriguez-Agudo, Daniel et al. (2007) Sulfated oxysterol, 25HC3S, is a potent regulator of lipid metabolism in human hepatocytes. Biochem Biophys Res Commun 360:802-8

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