Ontology highlight
ABSTRACT: Background
Aortic stenosis due to deleterious remodeling of the aortic valve is a health concern since it can be corrected only by valve replacement due to the poor knowledge of cellular mechanisms involved. Fibroblastic valvular interstitial cells (VICs) play a central role in valve leaflet stiffness by trans-differentiation into osteoblast-like cells leading to calcification. The TRPM4 (transient receptor potential melastatin 4) cation channel was shown to participate in cardiac fibroblast remodeling. It is also involved in radiation-induced aortic valve remodeling in vivo in mice. We hypothesized that TRPM4 might participate in human VIC transition to osteoblastic phenotype.Methods
Human aortic valves were collected from patients undergoing surgical valve replacement. Is
SUBMITTER: Aize M
PROVIDER: S-EPMC12132880 | biostudies-literature | 2025 Apr
REPOSITORIES: biostudies-literature