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Towards a Comprehensive Understanding of Platelet Activation and Platelet-monocyte Interaction: Multiple Proteomic Approaches in the Study of Atherosclerosis

机译:旨在全面了解血小板激活和血小板单核细胞相互作用:多种蛋白质组学方法研究动脉粥样硬化

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Multiple proteomic methods have been developed and applied on a model system studying platelet-monocyte interaction in the context of atherosclerosis. Monocyteactivated by platelet releasate leads to a systematic proteomic change over a long span of time. This includes short -term phosp horylation of signaling proteins, e.g. Rho GTPases, increased Reactive Oxygen Species production mediated by NADPH Oxidase and long-term up -regulation of membrane and glycoproteins with various biolo gical functions. This systematic proteomic approach will be applied on more complex systems in the future, e.g. platelet -monocyte aggregate, to achieve better understanding of the mechanism behind atherosclerosis leading to the discovery of potential drug target.
机译:已经开发了多种蛋白质组学方法,并应用于在动脉粥样硬化的背景下研究血小板单核细胞相互作用的模型系统。通过血小板释放的单核激活导致长跨度的系统蛋白质组学变化。这包括信号传导蛋白的短期 - Mposp Horlation,例如, rho GTP酶,NADPH氧化酶介导的反应性氧物种的增加和长期上调 - 具有各种Biolo GICIC功能的膜和糖蛋白的长期。这种系统蛋白质组学方法将在未来更复杂的系统上应用,例如,血小板 - 单胞细胞骨料,以更好地了解动脉粥样硬化后面的机制,导致潜在药物目标的发现。

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