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ABSTRACT: Objective
Calcific aortic valve disease (CAVD) is a significant cause of morbidity and mortality, which affects ≈1% of the US population and is characterized by calcific nodule formation and stenosis of the valve. Klotho-deficient mice were used to study the molecular mechanisms of CAVD as they develop robust aortic valve (AoV) calcification. Through microarray analysis of AoV tissues from klotho-deficient and wild-type mice, increased expression of the gene encoding cyclooxygenase 2 (COX2; Ptgs2) was found. COX2 activity contributes to bone differentiation and homeostasis, thus the contribution of COX2 activity to AoV calcification was assessed.Approach and results
In klotho-deficient mice, COX2 expression is increased throughout regions of valve calcification and is induc
SUBMITTER: Wirrig EE
PROVIDER: S-EPMC4979542 | biostudies-literature | 2015 Apr
REPOSITORIES: biostudies-literature