cardiovascular system
• at 3 weeks of age, 36% of mice show increased KLF2 expression in the endothelial cells, suggesting increased shear stress in the endothelial layer of aortic valves
• at 6 months of age, cellular features of diseased valves are consistent with a change toward a secretory valvular interstitial cell (VIC) phenotype
• however, no calcification is observed up to 9 months of age
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• partial fusion at the annulus of the aortic valve leaflets shows increased collagen deposition at the hinges covering the raphe
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• dysfunctional aortic valves exhibit thickened commissures
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• dysfunctional aortic valves have a reduced opening, occasionally in a 'fish mouth' pattern with only two visible leaflets, resembling a functional fused bicuspid aortic valve (BAV)-like phenotype
• aortic valves appear denser with localized accumulation of melanocyte clusters in the leaflets; the extracellular matrix (ECM) appears disorganized throughout the leaflets
• in the hinge regions, valves show smaller collagen type I fibers, cells reminiscent of osteoblasts and increased cellular debris
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• at 3 months of age, 38% of mice show aortic valve regurgitation and/or severe aortic stenosis
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• at 6 months of age, aortic valves tend to be thicker with cellular debris, small bundles of collagen fibers and abundant proteoglycans, esp. at the leaflet tip
• aortic valves are significantly thickened by 9 months
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• aortic valves are thickened at the hinge regions of the leaflets
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• mice exhibit progressive aortic valve dysfunction characterized by regurgitation and/or aortic stenosis
• at 3 months of age, ~20% of mice show abnormal blood flow in systole and increased systolic aortic pressure
• aortic peak pressures are significantly increased at 6 and 9 months of age
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• at 3 months of age, 27% of mice show aortic regurgitation in diastole; 38% of mice show aortic valve regurgitation and/or severe aortic stenosis
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Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
aortic valve disease | DOID:62 | J:287334 |