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血管损伤生物标志物的蛋白质组学鉴定

Proteomic identification of biomarkers of vascular injury.

作者信息

Huang Ngan F, Kurpinski Kyle, Fang Qizhi, Lee Randall J, Li Song

出版信息

Am J Transl Res. 2011 Feb;3(2):139-48. Epub 2010 Nov 21.

Abstract

Predictive biomarkers may be beneficial for detecting, diagnosing, and assessing the risk of restenosis and vascular injury. We utilized proteomic profiling to identify protein markers in the blood following vascular injury, and corroborated the differential protein expression with immunological approaches. Rats underwent carotid artery injury, and plasma was collected after 2 or 5 weeks. Proteomic profiling was carried out by two-dimensional differential in-gel electrophoresis. The differentially expressed plasma proteins were identified by mass spectroscopy and confirmed by immunoblotting. Proteomic profiling by two-dimensional differential in-gel electrophoresis and mass spectroscopy revealed plasma proteins that were differentially expressed at 2 weeks after injury. Among the proteins identified included vitamin D binding protein (VDBP), aldolase A (aldo A), and apolipoproteinE (apoE). Immunoblotting results validated a significant reduction in these proteins in the plasma at 2 or 5 weeks after vascular injury, in comparison to control animals without vascular injury. These findings suggest that VDBP, aldo A, and apoE may be biomarkers for vascular injury, which will have important prognostic and diagnostic implications.

摘要

预测性生物标志物可能有助于检测、诊断和评估再狭窄及血管损伤的风险。我们利用蛋白质组分析来识别血管损伤后血液中的蛋白质标志物,并通过免疫学方法证实差异蛋白质表达。对大鼠进行颈动脉损伤,在2周或5周后收集血浆。通过二维差异凝胶电泳进行蛋白质组分析。通过质谱鉴定差异表达的血浆蛋白,并通过免疫印迹进行确认。二维差异凝胶电泳和质谱分析的蛋白质组分析揭示了损伤后2周差异表达的血浆蛋白。鉴定出的蛋白质包括维生素D结合蛋白(VDBP)、醛缩酶A(aldo A)和载脂蛋白E(apoE)。免疫印迹结果证实,与未发生血管损伤的对照动物相比,血管损伤后2周或5周时这些蛋白质在血浆中的含量显著降低。这些发现表明,VDBP、aldo A和apoE可能是血管损伤的生物标志物,这将具有重要的预后和诊断意义。

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