Myocardial infarction or chronic cardiomyopathies can cause irreversible damage to the cardiac tissue. Recent evidence for multipotent cardiovascular stem cells has raised expectations that these cells may be engaged to heal the injured myocardium. However, the biological properties of cardiovascular stem cells are poorly understood, we know little about how disease limits the regenerative potential of stem cells and, we lack pharmaceuticals to guide stem cells toward forming new cardiac tissue. To address these issues, the Vanderbilt University Hub proposes three interacting projects (P1-P3), a Hub Core and a Consortium-wide Bioinformatics Core. PI will focus on the role of adult progenitor cells in normal cardiac homeostasis and after ischemic injury. P2 will explore the regenerative potential of endocardial progenitor cells. Whereas P3 will investigate how the disease environment affects the fate of progenitor cells in the heart. We have designed a pilot study to screen small molecular libraries for compounds that Induce endocardial and myocardial differentiation. Positive hits will be evaluated for effects on cardiac stem cells and myocardial repair. The Hub structure also incorporates a Core for standardized mouse models of myocardial injury and assessment of cardiac histology and function. Finally, we propose a Bioinformatics Core to organize Consortium data into a Stem Cell database to accelerate discovery, strength the connections between Consortium partners and facilitate the dissemination of information to the scientific community and the public. The Vanderbilt Hub will create a dynamic and interactive network of investigators to advance our knowledge about the biology of cardiovascular progenitor cells and their role in cardiac tissue repair. The proposed experiments will lead to novel molecular and cellular tools for the therapy of cardiovascular diseases.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01HL100398-04
Application #
8264177
Study Section
Special Emphasis Panel (ZHL1-CSR-J (S1))
Program Officer
Skarlatos, Sonia
Project Start
2009-09-30
Project End
2016-04-30
Budget Start
2012-05-01
Budget End
2013-04-30
Support Year
4
Fiscal Year
2012
Total Cost
$1,158,300
Indirect Cost
$444,562
Name
Vanderbilt University Medical Center
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Ryzhov, Sergey; Robich, Michael P; Roberts, Daniel J et al. (2018) ErbB2 promotes endothelial phenotype of human left ventricular epicardial highly proliferative cells (eHiPC). J Mol Cell Cardiol 115:39-50
Bylund, Jeffery B; Trinh, Linh T; Awgulewitsch, Cassandra P et al. (2017) Coordinated Proliferation and Differentiation of Human-Induced Pluripotent Stem Cell-Derived Cardiac Progenitor Cells Depend on Bone Morphogenetic Protein Signaling Regulation by GREMLIN 2. Stem Cells Dev 26:678-693
Kirabo, Annet; Ryzhov, Sergey; Gupte, Manisha et al. (2017) Neuregulin-1? induces proliferation, survival and paracrine signaling in normal human cardiac ventricular fibroblasts. J Mol Cell Cardiol 105:59-69
Markham, Larry W; Brinkmeyer-Langford, Candice L; Soslow, Jonathan H et al. (2017) GRMD cardiac and skeletal muscle metabolism gene profiles are distinct. BMC Med Genomics 10:21
Stephenson, Matthew K; Lenihan, Sean; Covarrubias, Roman et al. (2016) Scanning Electron Microscopy of Macerated Tissue to Visualize the Extracellular Matrix. J Vis Exp :
Bylund, Jeffery B; Hatzopoulos, Antonis K (2016) Differentiation of Atrial Cardiomyocytes from Pluripotent Stem Cells Using the BMP Antagonist Grem2. J Vis Exp :
Sysa-Shah, Polina; Tocchetti, Carlo G; Gupta, Manveen et al. (2016) Bidirectional cross-regulation between ErbB2 and ?-adrenergic signalling pathways. Cardiovasc Res 109:358-73
Favreau-Lessard, Amanda J; Ryzhov, Sergey; Sawyer, Douglas B (2016) Novel Biological Therapies Targeting Heart Failure: Myocardial Rejuvenation. Heart Fail Clin 12:461-71
Galindo, Cristi L; Soslow, Jonathan H; Brinkmeyer-Langford, Candice L et al. (2016) Translating golden retriever muscular dystrophy microarray findings to novel biomarkers for cardiac/skeletal muscle function in Duchenne muscular dystrophy. Pediatr Res 79:629-36
Rath, Rutwik; Lee, Jung Bok; Tran, Truc-Linh et al. (2016) Biomimetic microstructure morphology in electrospun fiber mats is critical for maintaining healthy cardiomyocyte phenotype. Cell Mol Bioeng 9:107-115

Showing the most recent 10 out of 45 publications