Critical Involvement of Calcium-Dependent Cytosolic Phospholipase A2α in Aortic Valve Interstitial Cell Calcification

被引:10
作者
Bonetti, Antonella [1 ]
Allegri, Lorenzo [2 ]
Baldan, Federica [2 ]
Contin, Magali [1 ]
Battistella, Claudio [3 ]
Damante, Giuseppe [2 ]
Marchini, Maurizio [1 ]
Ortolani, Fulvia [1 ]
机构
[1] Univ Udine, Dept Med, Histol & Electron Microscopy Unit, I-133100 Udine, Italy
[2] Univ Udine, Dept Med, Genet Unit, I-133100 Udine, Italy
[3] Univ Udine, Dept Med, Stat Unit, I-133100 Udine, Italy
关键词
cytosolic phospholipase A2 alpha; aortic valve calcification; aortic valve interstitial cell cultures; dexamethasone; ultrastructure; NONSPECIFIC ALKALINE-PHOSPHATASE; PROSTAGLANDIN E-2 GENERATION; SMOOTH-MUSCLE-CELLS; A(2); EXPRESSION; RELEASE; INDUCTION; STENOSIS; DIFFERENTIATION; MINERALIZATION;
D O I
10.3390/ijms21176398
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The involvement of calcium-dependent cytosolic phospholipase A2 alpha (cPLA2 alpha) in aortic valve calcification is not exhaustively elucidated. Here, cPLA2 alpha expression in aortic valve interstitial cell (AVIC) pro-calcific cultures simulating either metastatic or dystrophic calcification was estimated by qPCR, Western blotting, and counting of cPLA2 alpha-immunoreactive cells, with parallel ultrastructural examination of AVIC calcific degeneration. These evaluations also involved pro-calcific AVIC cultures treated with cPLA2 alpha inhibitor dexamethasone. cPLA2 alpha over-expression resulted for both types of pro-calcific AVIC cultures. Compared to controls, enzyme content was found to increase by up to 300% and 186% in metastatic and dystrophic calcification-like cultures, respectively. Increases in mRNA amounts were also observed, although they were not as striking as those in enzyme content. Moreover, cPLA2 alpha increases were time-dependent and strictly associated with mineralization progression. Conversely, drastically lower levels of enzyme content resulted for the pro-calcific AVIC cultures supplemented with dexamethasone. In particular, cPLA2 alpha amounts were found to decrease by almost 88% and 48% in metastatic and dystrophic calcification-like cultures, respectively, with mRNA amounts showing a similar trend. Interestingly, these drastic decreases in cPLA2 alpha amounts were paralleled by drastic decreases in mineralization degrees, as revealed ultrastructurally. In conclusion, cPLA2 alpha may be regarded as a crucial co-factor contributing to AVIC mineralization in vitro, thus being an attractive potential target for designing novel therapeutic strategies aimed to counteract onset or progression of calcific aortic valve diseases.
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页码:1 / 13
页数:13
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