首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Critical Involvement of Calcium-Dependent Cytosolic Phospholipase A2α in Aortic Valve Interstitial Cell Calcification
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Critical Involvement of Calcium-Dependent Cytosolic Phospholipase A2α in Aortic Valve Interstitial Cell Calcification

机译:钙依赖性胞质磷脂脂酶A2α在主动脉瓣间质细胞钙化中的临界累及

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摘要

The involvement of calcium-dependent cytosolic phospholipase A2α (cPLA2α) in aortic valve calcification is not exhaustively elucidated. Here, cPLA2α 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 cPLA2α-immunoreactive cells, with parallel ultrastructural examination of AVIC calcific degeneration. These evaluations also involved pro-calcific AVIC cultures treated with cPLA2α inhibitor dexamethasone. cPLA2α 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, cPLA2α 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, cPLA2α 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 cPLA2α amounts were paralleled by drastic decreases in mineralization degrees, as revealed ultrastructurally. In conclusion, cPLA2α 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.
机译:钙依赖性细胞溶质磷脂酶A2α(CPLA2α)在主动脉瓣膜钙化中的累积并未被详尽地阐明。这里,通过QPCR,Western印迹和计数CPLA2α-免疫反应细胞估算模拟转移性或营养钙化钙化的主动脉瓣间质细胞(AVIC)钙化培养物中的CPLA2α表达,具有平行的超微结构检查AVIC钙化变性的平行超微结构检查。这些评估还涉及用CPLA2α抑制剂地塞米松治疗的亲钙化腺培养物。 CPLA2α过表达导致两种类型的亲核化培养物。与对照相比,发现酶含量分别在转移性和营养不良钙化培养物中增加了高达300%和186%。也观察到mRNA量的增加,尽管它们与酶含量的含量不那么引人注目。此外,CPLA2α的增加是时间依赖性的,并且与矿化进展严格相关。相反,较低的酶含量水平较低,导致补充用地塞米松的亲钙化腺培养物。特别地,发现CPLA2α的量分别在转移和营养不良钙化培养物中降低近88%和48%,具有mRNA量显示出类似的趋势。有趣的是,CPLA2α的这些激烈减少量在矿化程度下的激烈减少平行,如超微结构的透露。总之,CPLA2α可以被认为是有助于在体外有助于AVIC矿化的关键因素,因此是设计新的治疗策略的有吸引力的潜在目标,旨在抵消钙化主动脉瓣疾病的发作或进展。

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