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狭窄三尖瓣和二叶式主动脉瓣患者主动脉局部差异的蛋白质组学研究。

Locally different proteome in aortas from patients with stenotic tricuspid and bicuspid aortic valves†.

机构信息

Department of Translational Medical Sciences, Università della Campania "L. Vanvitelli", Naples, Italy.

Cardiovascular Division, King's British Heart Foundation Centre, King's College London, London, UK.

出版信息

Eur J Cardiothorac Surg. 2019 Sep 1;56(3):458-469. doi: 10.1093/ejcts/ezz032.

Abstract

OBJECTIVES

We aimed to compare the intracellular proteome of ascending aortas from patients with stenotic bicuspid (BAV) and tricuspid aortic valves (TAV) to identify BAV-specific pathogenetic mechanisms of aortopathy and to verify the previously reported asymmetric expression of BAV aortopathy [concentrated at the convexity (CVX)] in its 'ascending phenotype' form.

METHODS

Samples were collected from the CVX and concavity sides of non-aneurysmal ascending aortas in 26 TAV and 26 BAV patients undergoing stenotic aortic valve replacement. Aortic lysates were subjected to cellular protein enrichment by subfractionation, and to proteome comparison by 2-dimensional fluorescence difference in-gel electrophoresis. Differentially regulated protein spots were identified by liquid chromatography-tandem mass spectrometry and analysed in silico. Selected results were verified by immunofluorescence and reverse transcription-polymerase chain reaction.

RESULTS

In BAV samples, 52 protein spots were differentially regulated versus TAV samples at the CVX and 10 spots at the concavity: liquid chromatography-tandem mass spectrometry identified 35 and 10 differentially regulated proteins, respectively. Charge trains of individual proteins (e.g. annexins) suggested the presence of post-translational modifications possibly modulating their activity. At the CVX, 37 of the 52 different protein spots showed decreased expression in BAV versus TAV. The affected biological pathways included those involved in smooth muscle cell contractile phenotype, metabolism and cell stress.

CONCLUSIONS

The observed differential proteomics profiles may have a significant impact on the pathogenesis of the aortopathy, pointing the way for further studies. At a preaneurysmal stage, an aorta with BAV shows more protein expression changes and potentially more post-translational modifications at the CVX of the ascending aorta than at the concavity, compared to that of TAV.

摘要

目的

我们旨在比较狭窄的二叶式主动脉瓣(BAV)和三叶式主动脉瓣(TAV)患者升主动脉的细胞内蛋白质组,以确定 BAV 主动脉病变的特定发病机制,并验证先前报道的 BAV 主动脉病变的不对称表达[集中在凸面(CVX)]在其“升主动脉表型”形式中。

方法

从 26 例 TAV 和 26 例 BAV 患者接受狭窄主动脉瓣置换术的非动脉瘤性升主动脉的 CVX 和凹面侧采集样本。主动脉裂解物通过亚部分分级进行细胞蛋白质富集,并通过 2 维荧光差异凝胶电泳进行蛋白质组比较。通过液相色谱-串联质谱法和计算机分析鉴定差异调节的蛋白质斑点。通过免疫荧光和逆转录聚合酶链反应验证选定的结果。

结果

在 BAV 样本中,CVX 处有 52 个蛋白质斑点与 TAV 样本差异调节,凹面处有 10 个斑点:液相色谱-串联质谱法分别鉴定出 35 个和 10 个差异调节蛋白。个体蛋白质的电荷轨迹(例如膜联蛋白)表明存在可能调节其活性的翻译后修饰。在 CVX 处,与 TAV 相比,52 个不同蛋白质斑点中的 37 个在 BAV 中表达下调。受影响的生物学途径包括涉及平滑肌细胞收缩表型、代谢和细胞应激的途径。

结论

观察到的差异蛋白质组学图谱可能对主动脉病变的发病机制有重大影响,为进一步研究指明了方向。在未发生动脉瘤的阶段,与 TAV 相比,BAV 的升主动脉 CVX 处的蛋白质表达变化和潜在的翻译后修饰更多,而凹面处则更多。

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