Cheow Esther Sok Hwee, Cheng Woo Chin, Lee Chuen Neng, de Kleijn Dominique, Sorokin Vitaly, Sze Siu Kwan
From the ‡School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive, Singapore 637551;
§Department of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, and Cardiovascular Research Institute, Singapore 119228;
Mol Cell Proteomics. 2016 Aug;15(8):2628-40. doi: 10.1074/mcp.M115.055731. Epub 2016 May 27.
Myocardial infarction (MI) triggers a potent inflammatory response via the release of circulatory mediators, including extracellular vesicles (EVs) by damaged cardiac cells, necessary for myocardial healing. Timely repression of inflammatory response are critical to prevent and minimize cardiac tissue injuries, nonetheless, progression in this aspect remains challenging. The ability of EVs to trigger a functional response upon delivery of carried bioactive cargos, have made them clinically attractive diagnostic biomarkers and vectors for therapeutic interventions. Using label-free quantitative proteomics approach, we compared the protein cargo of plasma EVs between patients with MI and from patients with stable angina (NMI). We report, for the first time, the proteomics profiling on 252 EV proteins that were modulated with >1.2-fold after MI. We identified six up-regulated biomarkers with potential for clinical applications; these reflected post-infarct pathways of complement activation (Complement C1q subcomponent subunit A (C1QA), 3.23-fold change, p = 0.012; Complement C5 (C5), 1.27-fold change, p = 0.087), lipoprotein metabolism (Apoliporotein D (APOD), 1.86-fold change, p = 0.033; Apolipoprotein C-III (APOCC3), 2.63-fold change, p = 0.029) and platelet activation (Platelet glycoprotein Ib alpha chain (GP1BA), 9.18-fold change, p < 0.0001; Platelet basic protein (PPBP), 4.72-fold change, p = 0.027). The data have been deposited to the ProteomeXchange with identifier PXD002950. This novel biomarker panel was validated in 43 patients using antibody-based assays (C1QA (p = 0.005); C5 (p = 0.0047), APOD (p = 0.0267); APOC3 (p = 0.0064); GP1BA (p = 0.0031); PPBP (p = 0.0465)). We further present that EV-derived fibrinogen components were paradoxically down-regulated in MI, suggesting that a compensatory mechanism may suppress post-infarct coagulation pathways, indicating potential for therapeutic targeting of this mechanism in MI. Taken together, these data demonstrated that plasma EVs contain novel diagnostic biomarkers and therapeutic targets that can be further developed for clinical use to benefit patients with coronary artery diseases (CADs).
心肌梗死(MI)通过循环介质的释放引发强烈的炎症反应,这些介质包括受损心脏细胞释放的细胞外囊泡(EVs),这对心肌愈合是必要的。及时抑制炎症反应对于预防和最小化心脏组织损伤至关重要,然而,在这方面的进展仍然具有挑战性。EVs在递送携带的生物活性货物时引发功能反应的能力,使其成为临床上有吸引力的诊断生物标志物和治疗干预载体。使用无标记定量蛋白质组学方法,我们比较了MI患者和稳定型心绞痛(NMI)患者血浆EVs的蛋白质货物。我们首次报告了对252种在MI后调节倍数>1.2倍的EV蛋白的蛋白质组学分析。我们鉴定出六种具有临床应用潜力的上调生物标志物;这些反映了梗死后期补体激活途径(补体C1q亚成分亚基A(C1QA),变化倍数3.23,p = 0.012;补体C5(C5),变化倍数1.27,p = 0.087)脂蛋白代谢(载脂蛋白D(APOD),变化倍数1.86,p = 0.033;载脂蛋白C-III(APOCC3),变化倍数2.63,p = 0.029)和血小板激活(血小板糖蛋白Ibα链(GP1BA),变化倍数9.18,p < 0.0001;血小板碱性蛋白(PPBP),变化倍数4.72,p = 0.027)。数据已存入ProteomeXchange,标识符为PXD002950。这个新的生物标志物面板在43名患者中使用基于抗体的检测方法进行了验证(C1QA(p = 0.005);C5(p = 0.0047),APOD(p = 0.0267);APOC3(p = 0.0064);GP1BA(p = 0.0031);PPBP(p = 0.0465))。我们进一步表明,EV衍生的纤维蛋白原成分在MI中反常地下调,这表明一种补偿机制可能抑制梗死后的凝血途径,这表明在MI中针对该机制进行治疗靶向的潜力。综上所述,这些数据表明血浆EVs包含新的诊断生物标志物和治疗靶点,可进一步开发用于临床,使冠状动脉疾病(CADs)患者受益。