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Identification of side- and shear-dependent microRNAs regulating porcine aortic valve pathogenesis

机译:鉴别副和剪切依赖性微小RNA调节猪主动脉瓣发病机制

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Aortic valve (AV) calcification is an inflammation driven process that occurs preferentially in the fibrosa. To explore the underlying mechanisms, we investigated if key microRNAs (miRNA) in the AV are differentially expressed due to disturbed blood flow (oscillatory shear (OS)) experienced by the fibrosa compared to the ventricularis. To identify the miRNAs involved, endothelial-enriched RNA was isolated from either side of healthy porcine AVs for microarray analysis. Validation using qPCR confirmed significantly higher expression of 7 miRNAs (miR-100, -130a, -181a/b, -199a-3p, -199a-5p, and -214) in the fibrosa versus the ventricularis. Upon bioinformatics analysis, miR-214 was selected for further investigation using porcine AV leaflets in an ex vivo shear system. Fibrosa and ventricularis sides were exposed to either oscillatory or unidirectional pulsatile shear for 2 days and 3 &7 days in regular and osteogenic media, respectively. Higher expression of miR-214, increased thickness of the fibrosa, and calcification was observed when the fibrosa was exposed to OS compared to the ventricularis. Silencing of miR-214 by anti-miR-214 in whole AV leaflets with the fibrosa exposed to OS significantly increased the protein expression of TGFβ1 and moderately increased collagen content but did not affect AV calcification. Thus, miR-214 is identified as a side- and shear-dependent miRNA that regulates key mechanosensitive gene in AV such as TGFβ1.
机译:主动脉瓣(AV)钙化是一种炎症驱动过程,其优先在纤维组中发生。为了探索潜在的机制,我们研究了AV中的键微小RNA(miRNA)是否由于纤维组经历的血流(振荡剪切(OS))与纤维组织的血流(振荡剪切(OS))进行差异表达。为了鉴定所涉及的miRNA,从健康猪AVS的任一侧分离内皮富集的RNA用于微阵列分析。使用QPCR的验证在纤维组中证实了7 miRNA(miR-100,-130a,-181a / b,-199a-3p,-199a -19a-5p和-214)的显着更高的表达。在生物信息学分析时,选择MIR-214用于在离体剪切系统中使用猪AV小叶进行进一步研究。在规则和骨质培养基中,将纤维组和腔室侧面暴露于振荡或单向脉冲剪切2天和3天和3天。 miR-214的表达更高,纤维纤维厚度增加,并且当与心室相比,当纤维组暴露于OS时,观察到纤维杆的厚度和钙化。通过暴露于OS暴露于OS的纤维组的整个AV传单中的抗miR-214沉默显着提高了TGFβ1的蛋白表达和中度增加的胶原含量,但不影响AV钙化。因此,miR-214被鉴定为副和剪切依赖性miRNA,其调节AV等TGFβ1中的关键机械敏感基因。

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