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血小板受体的程序性自体裂解

Programmed autologous cleavage of platelet receptors.

作者信息

Berndt M C, Karunakaran D, Gardiner E E, Andrews R K

机构信息

Department of Immunology, Monash University, Alfred Medical Research and Education Precinct, Melbourne, Vic., Australia.

出版信息

J Thromb Haemost. 2007 Jul;5 Suppl 1:212-9. doi: 10.1111/j.1538-7836.2007.02484.x.

Abstract

Platelet adhesion receptors play a critical role in vascular pathophysiology, and control platelet adhesion, activation and aggregation in hemostasis, thrombotic disease and atherogenesis. One of the key emerging mechanisms for regulating platelet function is the programmed autologous cleavage of platelet receptors. Induced by ligand binding or platelet activation, proteolysis at extracellular (ectodomain shedding) or intracellular (cytoplasmic domain deactivation) sites down-regulates the adheso-signaling function of receptors, thereby controlling not only platelet responsiveness, but in the case of ectodomain shedding, liberating soluble ectodomain fragments into plasma where they constitute potential modulators or markers. This review discusses the underlying mechanisms for dual proteolytic pathways of receptor regulation, and the impact of these pathways on thrombus formation and stability in vivo.

摘要

血小板黏附受体在血管病理生理学中发挥关键作用,并在止血、血栓形成疾病和动脉粥样硬化形成过程中控制血小板的黏附、激活和聚集。调节血小板功能的一个关键新兴机制是血小板受体的程序性自体裂解。由配体结合或血小板激活诱导,在细胞外(胞外域脱落)或细胞内(胞质域失活)位点的蛋白水解下调受体的黏附信号功能,从而不仅控制血小板反应性,而且在胞外域脱落的情况下,将可溶性胞外域片段释放到血浆中,在那里它们构成潜在的调节剂或标志物。本综述讨论了受体调节的双重蛋白水解途径的潜在机制,以及这些途径对体内血栓形成和稳定性的影响。

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