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- W2291511527 abstract "Aortic valve stenosis is a heart disease prevalent in the elderly characterized by valvular calcification, fibrosis, and inflammation, but its exact pathogenesis remains unclear. Previously, aortic valve stenosis was thought to be caused by chronic passive and degenerative changes associated with aging. However, recent studies have demonstrated that atherosclerotic processes and inflammation can induce valvular calcification and bone deposition, leading to valvular stenosis. In particular, the most abundant cell type in cardiac valves, valvular interstitial cells, can differentiate into myofibroblasts and osteoblast-like cells, leading to valvular calcification and stenosis. Differentiation of valvular interstitial cells can be trigged by inflammatory stimuli from several immune cell types, including macrophages, dendritic cells, T cells, B cells, and mast cells. This review indicates that crosstalk between immune cells and valvular interstitial cells plays an important role in the development of aortic valve stenosis." @default.
- W2291511527 created "2016-06-24" @default.
- W2291511527 creator A5039945599 @default.
- W2291511527 creator A5081063564 @default.
- W2291511527 date "2016-01-01" @default.
- W2291511527 modified "2023-10-10" @default.
- W2291511527 title "Involvement of Immune Cell Network in Aortic Valve Stenosis: Communication between Valvular Interstitial Cells and Immune Cells" @default.
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- W2291511527 doi "https://doi.org/10.4110/in.2016.16.1.26" @default.
- W2291511527 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4770097" @default.
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