Despite considerable advances in our understanding of the etiology of arteriosclerosis, about 30% cardiovascular disease (CVD) cannot be explained by traditional risk factors. Hyperhomocysteinemia (HHcy) is an important non-lipid CVD risk factor for which the underlying mechanism is unknown. We have previously proposed that Hcy promotes atherosclerosis by stimulating vascular smooth muscle cell proliferation and by inhibiting endothelial cell growth. To address the role of HHcy in an atherogenic background, we recently generated double knockout (KO) mice with targeted deletions of the genes for apolipoprotein E (apoE) and cystathionine b-synthase (CBS), which converts Hcy to cystathionine. Deletion of the CBS gene in apoE-/- mice resulted severe HHcy, which was associated with increased aortic lesions even in the absence of dietary manipulation. We therefore hypothesize that Hcy is a causative factor of atherosclerosis and causes macrophage activation and endothelial dysfunction. This project will study these hypothesis utilizing four linked specific aims. First, in Aim 1, experiments will evaluate HHcy atherosclerosis by examining early disease in aortic sinus in CBS/apoE double KO mice, and by studying post-injury atherosclerosis in CBS KO mice. Second, in Aim 2, studies are proposed to determine the effect of HHcy on macrophage function by bone marrow transplantation and by macrophage phagocytosis assay in the double KO mice. Third, in Aim 3, studies will characterize HHcy endothelial dysfunction and identify the mechanistic basis. Finally, in Aim 4, experiments will study atherosclerosis, functions of macrophage and endothelium following HHcy lowering therapy. We believe that the overall integrative approaches proposed will provide valuable new information to establish the links between Hcy and atherosclerosis.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL077288-06
Application #
7450953
Study Section
Vascular Cell and Molecular Biology Study Section (VCMB)
Program Officer
Ershow, Abby
Project Start
2004-07-15
Project End
2010-06-30
Budget Start
2008-07-01
Budget End
2010-06-30
Support Year
6
Fiscal Year
2008
Total Cost
$361,697
Indirect Cost
Name
Temple University
Department
Pharmacology
Type
Schools of Medicine
DUNS #
057123192
City
Philadelphia
State
PA
Country
United States
Zip Code
19122
Cueto, Ramon; Zhang, Lixiao; Shan, Hui Min et al. (2018) Identification of homocysteine-suppressive mitochondrial ETC complex genes and tissue expression profile - Novel hypothesis establishment. Redox Biol 17:70-88
Cheng, Zhongjian; Shen, Xinggui; Jiang, Xiaohua et al. (2018) Hyperhomocysteinemia potentiates diabetes-impaired EDHF-induced vascular relaxation: Role of insufficient hydrogen sulfide. Redox Biol 16:215-225
Xu, Yanjie; Xia, Jixiang; Liu, Suxuan et al. (2017) Endocytosis and membrane receptor internalization: implication of F-BAR protein Carom. Front Biosci (Landmark Ed) 22:1439-1457
Yang, Jiyeon; Fang, Pu; Yu, Daohai et al. (2016) Chronic Kidney Disease Induces Inflammatory CD40+ Monocyte Differentiation via Homocysteine Elevation and DNA Hypomethylation. Circ Res 119:1226-1241
Mai, Jietang; Nanayakkara, Gayani; Lopez-Pastrana, Jahaira et al. (2016) Interleukin-17A Promotes Aortic Endothelial Cell Activation via Transcriptionally and Post-translationally Activating p38 Mitogen-activated Protein Kinase (MAPK) Pathway. J Biol Chem 291:4939-54
Xi, Hang; Zhang, Yuling; Xu, Yanjie et al. (2016) Caspase-1 Inflammasome Activation Mediates Homocysteine-Induced Pyrop-Apoptosis in Endothelial Cells. Circ Res 118:1525-39
Liu, Suxuan; Xiong, Xinyu; Thomas, Sam Varghese et al. (2016) Analysis for Carom complex, signaling and function by database mining. Front Biosci (Landmark Ed) 21:856-72
Xie, Liping; Feng, Haihua; Li, Sha et al. (2016) SIRT3 Mediates the Antioxidant Effect of Hydrogen Sulfide in Endothelial Cells. Antioxid Redox Signal 24:329-43
Yin, Ying; Li, Xinyuan; Sha, Xiaojin et al. (2015) Early hyperlipidemia promotes endothelial activation via a caspase-1-sirtuin 1 pathway. Arterioscler Thromb Vasc Biol 35:804-16
Monroy, M Alexandra; Fang, Jianhua; Li, Shan et al. (2015) Chronic kidney disease alters vascular smooth muscle cell phenotype. Front Biosci (Landmark Ed) 20:784-95

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