Background: Cholesterol and bile acids have been implicated in playing important roles in several major diseases of """"""""Western Society"""""""" including: arteriosclerosis, cholesterol gallstone disease, cholestatic liver diseases, and colon cancer. The overall goal of this renewal application is aimed at a more detailed understanding of how the body regulates bile acid and cholesterol homeostasis, liver/intestinal physiology and determining if secondary bile acids are involved in the risk of cholesterol gallstone disease. The overall goal will be accomplished through the following specific aims: a) determine which cell signaling pathways are activated by bile acids in primary hepatocytes and which are important in regulating genes involved in cholesterol metabolism and phospholipid transport; b) determine if JNK-1 and JNK2 null mice are defective in cholesterol homeostatic mechanisms and if bile acid activated cell signaling pathways """"""""cross-talk"""""""" with bile acid activated nuclear receptors e.g., FXR (Dent, Hylemon); c) characterize in detail the FTF/HNF-4 site in the sterol 12alpha-hydroxylase (CYP8bl) promoter and elucidate the molecular mechanism by which FTF/SHP specifically regulates CYP8b1 transcription; d) characterize the molecular mechanism involved in the SREBP-2 mediated suppression of the CYP8B1 promoter; e) characterize the significance and physiological role SREB-2-mediated suppression of CYP8b1 (Gil); f) determine the role of steroidogenic acute regulatory (StAR) protein and other intracellular cholesterol transport proteins (SCP-2, MLN64) play in the regulation of bile acid synthesis in the liver; g) determine if StAR is expressed in the liver (Pandak,Gil); h) determine the 3 dimensional (3D) structure and catalytic mechanism of bile acid 7alpha and 7beta-dehydratase from Clostridium scindens; i) express, purify, and characterize a novel 3-oxo-delta4steroid oxidoreductase from C. scindens; j) clone, sequence, and analyze the bai operon from Clostridium hylemonae TN271; k) isolate, characterize, and identify cholic acid 7alpha-dehydroxylating bacteria from cholesterol gallstone patients with high (>30%) deoxycholic acid and controls; and I) determine if gallstone patients are colonized by unique species of 7alpha-dehydroxylating bacteria. (Hylemon, Heuman).

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Program Projects (P01)
Project #
5P01DK038030-17
Application #
6665224
Study Section
Special Emphasis Panel (ZDK1-GRB-1 (M1))
Program Officer
Serrano, Jose
Project Start
1986-12-01
Project End
2007-08-31
Budget Start
2003-09-01
Budget End
2004-08-31
Support Year
17
Fiscal Year
2003
Total Cost
$929,594
Indirect Cost
Name
Virginia Commonwealth University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
105300446
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
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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
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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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