Cardiovascular disease is a leading cause of morbidity and mortality in the United States. Atherosclerosis is an inflammatory disease of the large and mid-sized arteries that promotes the development of cardiovascular disease through plaque formation, restricted blood flow, and ultimately thrombotic events. Chronic exposure of the arterial endothelium to elevated (and potentially modified) serum cholesterol leads to the hallmarks of pathology; including altered blood flow patterns, endothelial activation, and recruitment of blood monocytes. Infiltrating monocytes differentiate into lipid-laden plaque macrophages and contribute to the necrotic core that is a hallmark of advanced lesions. Research has focused on the role of monocytes in the maintenance of atherosclerotic plaques however; relatively few resources have been dedicated to investigating the role of tissue-resident mononuclear phagocytes (MNPs), which reside in the aortic arch. Resident MNPs reside in the nascent aorta at birth in locations where plaques have propensity to develop, and the cells are even present there in animals not susceptible to disease. My preliminary studies definitively show these cells are macrophage lineage cells, not dendritic cells as previously reported and may facilitate the onset of early plaque by importing the first quantitative load of cholesterol into the intima. Thus, these cells may be pivotal in regulating atherosclerotic plaque burden. However, technical approaches to determine if intimal resident macrophages persist in plaques and carry out distinct roles have not emerged to address this possibility. I have established protocols to track and modulate the resident intimal macrophage population independent of infiltrating blood-derived precursors like monocytes. I find that resident macrophages are the first cells to take up lipid in the aortic wall and persist through plaque development. Resident macrophages reside inside regions known to develop into necrotic core, and also form a ?boarder? around the plaque itself. Further, I have developed approaches to track proliferation of macrophages within the plaque, as well as use new technologies to isolate intimal macrophages without contamination from monocytes or adventitial macrophages. Primarily using a combination of fixed- and live-imaging approaches in murine atherosclerotic plaque and taking advantage of new mouse models, I will test the hypothesis that resident aortic intimal macrophages, independent of recruited monocyte-derived macrophages, play a unique and important role in atherosclerotic plaque development. To test my hypothesis, I will assess the role of proliferation and motility in the plaques, address the differential roles of resident versus recruited monocytes in disease progression, and further develop intravital approaches to understand how interactions between monocytes and intimal macrophages may contribute to disease severity. If true, the implications of this study would greatly clarify and alter how the field might target macrophages or circulating monocytes to manage atherosclerotic disease.

Public Health Relevance

Atherosclerosis is an underlying disease associated with most cardiovascular diseases including stroke, high blood pressure, and thrombosis. Atherosclerosis is driven by chronic exposure to elevated serum cholesterol levels which leads activation of vascular endothelium, deposition of lipid and inflammatory cells within the intimal layer of the artery, creating an atherosclerotic plaque. Macrophages are central mediators of disease progression within the plaque, primarily through uptake of cholesterol and production pro-inflammatory cytokines. Given the centrality of macrophages to disease, it is necessary to understand from where macrophages originate (tissue resident versus recruited), genetic profiles associated with maturing plaque macrophages, and arrangement and localization of macrophages within differing regions of the atherosclerotic plaque. These insights will be valuable for developing therapeutics for attenuating inflammatory responses in atherosclerosis.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Career Transition Award (K99)
Project #
1K99HL138163-01A1
Application #
9526863
Study Section
NHLBI Mentored Transition to Independence Review Committee (MTI)
Program Officer
Huang, Li-Shin
Project Start
2018-03-09
Project End
2020-02-29
Budget Start
2018-03-09
Budget End
2019-02-28
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Washington University
Department
Pathology
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Williams, Jesse W; Martel, Catherine; Potteaux, Stephane et al. (2018) Limited Macrophage Positional Dynamics in Progressing or Regressing Murine Atherosclerotic Plaques-Brief Report. Arterioscler Thromb Vasc Biol 38:1702-1710
Williams, Jesse W; Giannarelli, Chiara; Rahman, Adeeb et al. (2018) Macrophage Biology, Classification, and Phenotype in Cardiovascular Disease: JACC Macrophage in CVD Series (Part 1). J Am Coll Cardiol 72:2166-2180