This project will test the hypothesis that reactive oxygen species (ROS) accumulation in aortic smooth muscle cells (SMCs) mediates the aortopathy in patients with bicuspid aortic valve (BAV). The interdisciplinary investigative team possesses a unique composition of expertise and has devised a novel approach to prove that ROS accumulation in BAV-ascending aortic aneurysm (TAA) specimens leads to de-differentiation of SMCs, abnormal extracellular matrix (ECM) composition and architecture and altered biomechanical strength of the aortic wall. The hypothesis is supported by the team's strong preliminary data demonstrating ROS accumulation, reduced cell viability in the presence of ROS, diminished oxidative stress responses, de- differentiation of SMCs, disrupted matrix architecture and altered biomechanical tensile and delamination strengths in the ascending aorta of BAV patients compared with tricuspid aortic valve (TAV)-TAA and non- aneurysmal patients. The innovative strategy is accomplished in a two-aim approach: 1) Define what changes in SMC phenotype, ECM composition and architecture, and biomechanical tensile and delamination strengths are associated with ROS accumulation in BAV aortopathy and 2) Prove that ROS accumulation in aortic SMCs mediates the BAV aortopathy. This study will exploit 1) the PI's extensive tissue bank of human ascending aortic specimens and primary SMCs isolated from the following patient cohorts: a) BAV-TAA compared with b) non-aneurysmal BAV, c) TAV-TAA, and d) non-aneurysmal TAV normal; and 2) the team's established scaffold-based 3-D tissue culture model. ROS will be evaluated using the investigators' expertise in electron paramagnetic resonance spin trapping and confocal microscopy of fluorescence-based ROS probes. Innovative assessment of ECM composition and architecture will be achieved using multi-photon microscopy with second harmonic generation to define alignment of collagen and elastin fibers, histological detection of collagen and elastin, and quantification of MMP activity. The team's pioneering techniques for studying blood vessel biomechanics will be utilized throughout the research design. This study will, for the first time, define and prove that ROS mechanisms mediate the BAV aortopathy. The results will potentiate significant long-term clinical benefits including the development of improved diagnostic tools for earlier detection and better surveillance of the BAV aortopathy and the discovery of pharmacologic therapies directed at modulation of ROS in the aortic wall to prevent aneurysm formation in BAV patients.

Public Health Relevance

Bicuspid aortic valve (BAV) occurs in 1-2% of the population. The ascending aortas of BAV patients are uniformly larger in diameter compared to age- and sex-matched controls, and 45% percent of individuals requiring surgery to replace the ascending aorta because of thoracic aortic aneurysm or dissection have the congenital defect of BAV. Due to a lack of understanding of BAV-associated aortopathy at the cellular and molecular level, care of BAV patients has been limited to surgery only after the end-stage development of aneurysm or dissection thus resulting in a significant clinical problem worldwide: the hospital mortality rate after ascending aortic dissection is over 23% with and over 60% without surgical intervention representing the fifteenth leading cause of death in the United States. Discovery of the mechanism mediating BAV aortopathy will potentiate significant long-term clinical benefits including 1) the development of improved diagnostic tools for earlier detection and better surveillance and 2) the discovery of pharmacologic therapies to preserve aortic wall architecture and integrity to prevent aneurysm formation in BAV patients.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
4R01HL109132-05
Application #
9058113
Study Section
Bioengineering, Technology and Surgical Sciences Study Section (BTSS)
Program Officer
Tolunay, Eser
Project Start
2012-05-01
Project End
2017-04-30
Budget Start
2016-05-01
Budget End
2017-04-30
Support Year
5
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of Pittsburgh
Department
Surgery
Type
Schools of Medicine
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Thunes, James R; Phillippi, Julie A; Gleason, Thomas G et al. (2018) Structural modeling reveals microstructure-strength relationship for human ascending thoracic aorta. J Biomech 71:84-93
Billaud, Marie; Hill, Jennifer C; Richards, Tara D et al. (2018) Medial Hypoxia and Adventitial Vasa Vasorum Remodeling in Human Ascending Aortic Aneurysm. Front Cardiovasc Med 5:124
Venkatesh, Premakumari; Phillippi, Julie; Chukkapalli, Sasanka et al. (2017) Aneurysm-Specific miR-221 and miR-146a Participates in Human Thoracic and Abdominal Aortic Aneurysms. Int J Mol Sci 18:
Hall, Alexander; Chan, Patrick; Sheets, Kevin et al. (2017) Nanonet force microscopy for measuring forces in single smooth muscle cells of the human aorta. Mol Biol Cell 28:1894-1900
Phillippi, Julie A; Hill, Jennifer C; Billaud, Marie et al. (2017) Bicuspid Aortic Valve Morphotype Correlates With Regional Antioxidant Gene Expression Profiles in the Proximal Ascending Aorta. Ann Thorac Surg 104:79-87
Billaud, Marie; Phillippi, Julie A; Kotlarczyk, Mary P et al. (2017) Elevated oxidative stress in the aortic media of patients with bicuspid aortic valve. J Thorac Cardiovasc Surg 154:1756-1762
Fercana, George R; Yerneni, Saigopalakrishna; Billaud, Marie et al. (2017) Perivascular extracellular matrix hydrogels mimic native matrix microarchitecture and promote angiogenesis via basic fibroblast growth factor. Biomaterials 123:142-154
Billaud, Marie; Donnenberg, Vera S; Ellis, Bradley W et al. (2017) Classification and Functional Characterization of Vasa Vasorum-Associated Perivascular Progenitor Cells in Human Aorta. Stem Cell Reports 9:292-303
Thunes, James R; Pal, Siladitya; Fortunato, Ronald N et al. (2016) A structural finite element model for lamellar unit of aortic media indicates heterogeneous stress field after collagen recruitment. J Biomech 49:1562-1569
Tsamis, Alkiviadis; Phillippi, Julie A; Koch, Ryan G et al. (2016) Extracellular matrix fiber microarchitecture is region-specific in bicuspid aortic valve-associated ascending aortopathy. J Thorac Cardiovasc Surg 151:1718-1728.e5

Showing the most recent 10 out of 19 publications