Coronary artery disease (CAD), the direct result of atherosclerosis, is the most common cause of death in people over the age of 65. Although, statins have been used to lower LDL and retard disease progression, these drugs have modest impact on lesion burden as reflected by the degree of regression seen in the REVERSAL and recent ASTEROID studies and the still substantial rates of heart attacks in large-scale clinical trials of these drugs. By understanding the factors that lead to plaque regression, better treatment options may be developed for many at risk, especially the older population, who already carry a heavy plaque burden. My supervisor, Dr. Edward Fisher, has led the development of in-vivo regression models using surgical and genetic approaches to the standard models of atherosclerosis progression. Using laser capture microscopy to capture foam cells, important mediators in plaque pathophysiology, we studied gene expression changes specifically in these cells in plaques. We showed that CCR7, an established maturation marker for dendritic cells that promotes their emigration from tissues to lymph nodes, was functionally required to promote regression in intermediate lesions, the type that most resembles the ones most prone to rupture and cause an acute myocardial infarction in people. Since members of the aging population with CAD have these lesions, we propose to 1) establish the functional requirement for CCR7 in regression by using a different in vivo approach and 2) determine the molecular mechanisms inducing CCR7 gene expression. Ultimately, the results obtained from the proposed studies may represent a novel path towards achieving regression of atherosclerosis in the aging, a population expanding due to the average life-span increasing. Coronary artery disease (CAD), the direct result of atherosclerosis, is an age-related disorder with a tremendous impact on public health. Although retarding the progression is important, this will not eliminate the huge plaque burden already present in the elderly. With regression models and the tools to analyze them on a molecular level, there is the exciting potential to identify factors that can be manipulated to accelerate regression in patients at risk for CAD, most of whom are members of the older population. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Individual Predoctoral NRSA for M.D./Ph.D. Fellowships (ADAMHA) (F30)
Project #
5F30AG029748-02
Application #
7570666
Study Section
Special Emphasis Panel (ZRG1-F10-H (20))
Program Officer
Kohanski, Ronald A
Project Start
2007-02-12
Project End
2011-02-11
Budget Start
2008-03-15
Budget End
2009-02-11
Support Year
2
Fiscal Year
2008
Total Cost
$45,972
Indirect Cost
Name
New York University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
Feig, Jonathan E; Feig, Jessica L; Dangas, George D (2016) The role of HDL in plaque stabilization and regression: basic mechanisms and clinical implications. Coron Artery Dis 27:592-603
Feig, Jonathan E (2014) Regression of atherosclerosis: insights from animal and clinical studies. Ann Glob Health 80:13-23
Feig, Jonathan E; Hewing, Bernd; Smith, Jonathan D et al. (2014) High-density lipoprotein and atherosclerosis regression: evidence from preclinical and clinical studies. Circ Res 114:205-13
Ramsey, Stephen A; Vengrenyuk, Yuliya; Menon, Prashanthi et al. (2014) Epigenome-guided analysis of the transcriptome of plaque macrophages during atherosclerosis regression reveals activation of the Wnt signaling pathway. PLoS Genet 10:e1004828
Feig, Jonathan E; Fisher, Edward A (2013) Laser capture microdissection for analysis of macrophage gene expression from atherosclerotic lesions. Methods Mol Biol 1027:123-35
Rong, James X; Blachford, Courtney; Feig, Jonathan E et al. (2013) ACAT inhibition reduces the progression of preexisting, advanced atherosclerotic mouse lesions without plaque or systemic toxicity. Arterioscler Thromb Vasc Biol 33:4-12
Wanschel, Amarylis; Seibert, Tara; Hewing, Bernd et al. (2013) Neuroimmune guidance cue Semaphorin 3E is expressed in atherosclerotic plaques and regulates macrophage retention. Arterioscler Thromb Vasc Biol 33:886-93
Feig, Jonathan E; Feig, Jessica L (2012) Macrophages, dendritic cells, and regression of atherosclerosis. Front Physiol 3:286
Feig, Jonathan E; Vengrenyuk, Yuliya; Reiser, Vladimir et al. (2012) Regression of atherosclerosis is characterized by broad changes in the plaque macrophage transcriptome. PLoS One 7:e39790
Feig, Jonathan E; Parathath, Sajesh; Rong, James X et al. (2011) Reversal of hyperlipidemia with a genetic switch favorably affects the content and inflammatory state of macrophages in atherosclerotic plaques. Circulation 123:989-98

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