Role of TGFbeta Ligand Function in the Development and Pathogenesis of Cardiovascular Disease
A special issue of Journal of Cardiovascular Development and Disease (ISSN 2308-3425). This special issue belongs to the section "Basic and Translational Cardiovascular Research".
Deadline for manuscript submissions: closed (31 December 2022) | Viewed by 2596
Special Issue Editors
Interests: transforming growth factor; cardiovascular development; valve development; valvular heart disease; aortic aneurysm; aortic calcification
Special Issues, Collections and Topics in MDPI journals
Interests: abdominal aortic aneurysm
Interests: aortic valve; heart valve diseases; vascular surgery; aneurysm cardiac surgery; aortic diseases; atherosclerotic vascular diseases; cardiovascular surgery; coronary artery bypass surgery; endovascular surgery
Special Issues, Collections and Topics in MDPI journals
Special Issue Information
Dear Colleagues,
We welcome review and original article contributions that increase our understanding of the transforming growth factor beta (TGFB) pathway in cardiovascular development and disease. TGFB ligands (TGFB1,2,3) are multifunctional growth factors and cytokines that are produced in latent form by most cardiac cell types during cardiovascular development and in adult cardiovascular tissues. All TGFB ligands bind to the TGFBR1 and TGFBR2 receptor complex. Downstream signaling occurs through phosphorylation and nuclear translocation of SMAD2 and SMAD3 in conjunction with SMAD4. In addition, the TGFB ligand–receptor complex also activates non-canonical pathways involving the MAP kinase pathway (TAK, p38, ERK1/2 MAPK). TGFB-regulated gene expression controls cell differentiation, cell growth, apoptosis, cell migration, and extracellular matrix production and remodeling during cardiovascular development and pathogenesis of cardiovascular disease. Genetic mutations in TGFB2 and TGFB3 cause congenital heart disease, bicuspid aortic valve, mitral valve disease, and aortic aneurysm and dissection in patients of Loeys–Dietz syndrome. Increased TGFB1 expression is associated with cardiomyopathy, mitral valve prolapse, and aortic aneurysm in Marfan syndrome. Increased TGFB signaling is found in cardiac fibrosis, cardiac hypertrophy, myocardial infarction and heart failure, hypertension, atherosclerosis, arterial calcification, and thoracic and abdominal aortic aneurysms. Thus, understanding the cell-specific role and molecular and biochemical mechanisms of TGFβ ligands will lead to safer and more effective therapy for cardiovascular disease. Consequently, we invite author contributions that advance our current understanding of TGFβ signaling in cardiovascular development and cardiovascular disease. We suggest the following themes for this Special Issue:
- TGFβ in cardiovascular development;
- TGFβ in aortopathy: thoracic and abdominal aneurysm, arterial calcification, atherosclerosis;
- TGFβ in bicuspid aortic valve, mitral valve disease, aortic valve calcification, aortic stenosis;
- TGFβ in cardiac hypertrophy, cardiac fibrosis, heart failure;
- TGFβ in hypertension and atherosclerosis;
- TGFβ signaling mechanism using in vitro cell and tissue culture models;
- Novel models of TGFβ signaling in the cardiovascular system;
TGFβ-based therapies of cardiovascular disease and cardiotoxicity.
Dr. Mohamad Azhar
Dr. Chetan Hans
Dr. Nimrat Grewal
Guest Editors
Manuscript Submission Information
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Keywords
- transforming growth factor beta
- TGFB1
- TGFB2
- TGFB3
- aortic valve
- aneurysm
- mitral valve
- congenital heart disease
- fibrosis
- hypertrophy
- hypertension
- atherosclerosis
- peripheral artery disease
- heart failure
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