Project Grant R01HL173543

Award Date 5/15/25
Completion Date 3/31/29
Dollars Obligated $640K
Federal Grant Program
93.837
Assistance Type
Project Grant
Place of Performance
Cleveland, OH 44195, USA
Similar Awards
This Project Grant award from the National Heart, Lung, and Blood Institute (NHLBI), under the Cardiovascular Diseases Research program (CFDA 93.837), will support research to uncover effective strategies for mitigating the detrimental effects of cardiac fibrosis in diseases like dilated cardiomyopathy (DCM). The $159,512 award will fund the validation and description of the anti-fibrotic mechanisms of two drug compounds, CGS15943 and AM404, in a mouse model of LMNA-related DCM. The research...
The National Heart, Lung, and Blood Institute (NHLBI) awarded a $587,749 Project Grant under the Cardiovascular Diseases Research program (CFDA 93.837) to the Regents of the University of Minnesota. The objective of this 4-year grant, with a performance period from July 1, 2024 to April 30, 2028, is to investigate the role of endoplasmic reticulum-mitochondria contact sites in right ventricular fibrosis. The research aims to establish the molecular mechanisms by which C-Src-dependent...
This federal Project Grant award, valued at $616,000.00 and funded by the National Heart, Lung, and Blood Institute (NHLBI) under the Cardiovascular Diseases Research program (CFDA 93.837), supports research at Northwestern University to investigate the role of mitochondrial metabolism in alveolar epithelial cell differentiation and the development of lung fibrosis. The funded project aims to determine whether an increased mitochondrial NADH/NAD+ ratio and activation of the integrated stress...
The federal Project Grant award R01HL174940, totaling $785,198, was provided by the National Heart, Lung, and Blood Institute (NHLBI) under the Cardiovascular Diseases Research grant program (CFDA 93.837). The grant supports research to investigate the role of chaperone-mediated autophagy (CMA) in regulating the function and phenotypic transitions of fibroblasts and myofibroblasts during cardiac tissue repair and remodeling following myocardial infarction. The project aims to study how CMA...
The National Heart, Lung, and Blood Institute (NHLBI) awarded the University of Alabama at Birmingham (UAB) a $561,392 Project Grant under the Cardiovascular Diseases Research program (CFDA 93.837) to investigate the role of RNA methylation in cardiac fibrosis and heart failure progression. The key objectives of this 4-year research project are to: 1) Investigate the direct link between the RNA methyltransferase METTL3 activation and cardiac fibrosis progression using a fibroblast-specific...
The National Heart, Lung, and Blood Institute (NHLBI) awarded a $756,947 Project Grant under the Cardiovascular Diseases Research program (CFDA 93.837) to the University of Utah. The funding will support a 4-year research project to "Assess Myocardial Fibrosis with Spin Locked MRI". The key objectives are to: 1) Study the value of different T1rho MRI techniques and conventional MRI methods in preclinical models of diffuse and focal myocardial fibrosis; 2) Develop and validate new...
This Project Grant award from the National Heart, Lung, and Blood Institute (NHLBI), under the Cardiovascular Diseases Research program (CFDA 93.837), will provide $655,636 to the Texas Heart Institute (THI) to investigate cardiac fibroblast mechanisms in single ventricle disease (CVD) and heart failure. The key objectives are to gain insights into CVD pathology and uncover new therapeutic targets, with the long-term goal of promoting productive heart repair in failing CVD hearts. The research...
This Project Grant award from the National Heart, Lung, and Blood Institute (NHLBI), part of the National Institutes of Health, under the Cardiovascular Diseases Research federal grant program (CFDA 93.837), will fund research to investigate the effects of neprilysin inhibition on myocardial interstitial fibrosis, a key contributor to heart failure with preserved ejection fraction (HFPEF). The $195,480 award will support a 5-year study led by Dr. Cunningham at Brigham and Women's Hospital, a...
The National Heart, Lung, and Blood Institute (NHLBI) awarded a $170,555 Project Grant under the Cardiovascular Diseases Research program (CFDA 93.837) to The Washington University in St. Louis. The grant, awarded on July 24, 2024, will fund research to investigate the feasibility of using chimeric antigen receptor (CAR) T cells targeting fibroblast activation protein (FAP) as a novel therapy for cardiac fibrosis. The project aims to delineate the effects of FAP CAR T cells on myocardial...
This Project Grant award from the National Heart, Lung, and Blood Institute (NHLBI), under the Cardiovascular Diseases Research federal grant program (CFDA 93.837), provides $125,250 to The General Hospital Corporation (Massachusetts General Hospital) to conduct a 2-year research project. The project, led by Dr. James Rhee, will investigate the role of the cytokine FAM3D in regulating cardiac fibrosis and inflammation in heart failure. The research aims to elucidate how FAM3D affects cardiac...

This federal Project Grant award from the National Heart, Lung, and Blood Institute (NHLBI), under the Cardiovascular Diseases Research program (CFDA 93.837), is supporting research to investigate the role of mitochondrial signaling between cardiomyocytes and cardiac fibroblasts in the pathogenesis of cardiac fibrosis. The $639,621 award to the Cleveland Clinic Lerner College of Medicine of Case Western Reserve University will fund a 4-year research project to test the hypothesis that intact mitochondria serve as transcellular signaling conduits between cardiomyocytes and fibroblasts, promoting myofibroblast differentiation and contributing to cardiac fibrosis. The research employs a range of ex vivo tools, reagents, and genetically engineered mouse models to examine the regulation of mitochondrial release from cardiomyocytes, the necessity and sufficiency of fibroblast mitochondrial uptake in driving myofibroblast differentiation, and the underlying signaling pathways involved. This work aims to advance the understanding of cardiomyocyte-fibroblast crosstalk and its role in cardiac fibrosis, with potential implications for developing new therapeutic strategies.

Generated 6/17/25, 4:58 AM