Suppr超能文献

通过蛋白质组学分析寻找新型心血管生物标志物。

Quest for novel cardiovascular biomarkers by proteomic analysis.

作者信息

Vivanco Fernando, Martín-Ventura Jose L, Duran Mari Carmen, Barderas Maria G, Blanco-Colio Luis, Dardé Verónica M, Mas Sebastián, Meilhac Olivier, Michel Jean B, Tuñón Jose, Egido Jesús

机构信息

Department of Immunology, Vascular Research Laboratory, Fundación Jiménez Diaz, Autónoma University, Avenida Reyes Católicos 2, 28040 Madrid, Spain.

出版信息

J Proteome Res. 2005 Jul-Aug;4(4):1181-91. doi: 10.1021/pr0500197.

Abstract

Atherosclerosis, and the resulting coronary heart disease and stroke, is the most common cause of death in developed countries. Atherosclerosis is an inflammatory process that results in the development of complex lesions or plaques that protrude into the arterial lumen. Plaque rupture and thrombosis result in the acute clinical complications of myocardial infarction (MI) and stroke. Although certain risk factors (dyslipidemias, diabetes, hypertension) and humoral markers of plaque vulnerability (C-reactive protein, interleukin-6, 10 and 18, CD40L) have been identified, a highly sensitive and specific biomarker or protein profile, which could provide information on the stability/vulnerability of atherosclerotic lesions, remains to be identified. In this review, we report several proteomic approaches which have been applied to circulating or resident cells, atherosclerotic plaques or plasma, in the search for new proteins that could be used as cardiovascular biomarkers. First, an example using a differential proteomic approach (2-DE and MS) comparing the secretome from control mammary arteries and atherosclerotic plaques is displayed. Among the different proteins identified, we showed that low levels of HSP-27 could be a potential marker of atherosclerosis. Second, we have revised several studies performed in cells involved in the pathogenesis of atherosclerosis (foam cells and smooth muscle cells). Another approach consists of performing proteomic analysis on circulating cells or plasma, which will provide a global view of the whole body response to atherosclerotic aggression. Circulating cells can bear information reflecting directly an inflammatory or pro-coagulant state related to the pathology. As an illustration, we report that circulating monocytes and plasma in patients with acute coronary syndromes has disclosed that mature Cathepsin D is increased both in the plasma and monocytes of these patients. Finally, the problems of applying proteomic approach directly to plasma will be discussed. The purpose of this review is to provide the reader with an overview of different proteomic approaches that can be used to identify new biomarkers in vascular diseases.

摘要

动脉粥样硬化以及由此引发的冠心病和中风,是发达国家最常见的死亡原因。动脉粥样硬化是一种炎症过程,会导致形成突出于动脉管腔的复杂病变或斑块。斑块破裂和血栓形成会引发心肌梗死(MI)和中风等急性临床并发症。尽管已经确定了某些危险因素(血脂异常、糖尿病、高血压)以及斑块易损性的体液标志物(C反应蛋白、白细胞介素-6、10和18、CD40L),但仍有待确定一种能够提供动脉粥样硬化病变稳定性/易损性信息的高灵敏度和特异性生物标志物或蛋白质谱。在本综述中,我们报告了几种蛋白质组学方法,这些方法已应用于循环细胞或驻留细胞、动脉粥样硬化斑块或血浆,以寻找可作为心血管生物标志物的新蛋白质。首先,展示了一个使用差异蛋白质组学方法(二维电泳和质谱)比较对照乳腺动脉和动脉粥样硬化斑块分泌组的例子。在鉴定出的不同蛋白质中,我们发现低水平的热休克蛋白-27可能是动脉粥样硬化的潜在标志物。其次,我们回顾了在参与动脉粥样硬化发病机制的细胞(泡沫细胞和平滑肌细胞)中进行的几项研究。另一种方法是对循环细胞或血浆进行蛋白质组学分析,这将提供全身对动脉粥样硬化侵袭反应的整体视图。循环细胞可以携带直接反映与该病理相关的炎症或促凝状态的信息。例如,我们报告急性冠状动脉综合征患者的循环单核细胞和血浆显示,这些患者的血浆和单核细胞中成熟组织蛋白酶D均增加。最后,将讨论直接将蛋白质组学方法应用于血浆的问题。本综述的目的是为读者提供不同蛋白质组学方法概述,这些方法可用于识别血管疾病中的新生物标志物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验