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止血的新基础。

New fundamentals in hemostasis.

机构信息

Einthoven Laboratroy for Experimental Vascular Medicine, Leiden University Medical Center, Leiden, The Netherlands.

出版信息

Physiol Rev. 2013 Jan;93(1):327-58. doi: 10.1152/physrev.00016.2011.

Abstract

Hemostasis encompasses the tightly regulated processes of blood clotting, platelet activation, and vascular repair. After wounding, the hemostatic system engages a plethora of vascular and extravascular receptors that act in concert with blood components to seal off the damage inflicted to the vasculature and the surrounding tissue. The first important component that contributes to hemostasis is the coagulation system, while the second important component starts with platelet activation, which not only contributes to the hemostatic plug, but also accelerates the coagulation system. Eventually, coagulation and platelet activation are switched off by blood-borne inhibitors and proteolytic feedback loops. This review summarizes new concepts of activation of proteases that regulate coagulation and anticoagulation, to give rise to transient thrombin generation and fibrin clot formation. It further speculates on the (patho)physiological roles of intra- and extravascular receptors that operate in response to these proteases. Furthermore, this review provides a new framework for understanding how signaling and adhesive interactions between endothelial cells, leukocytes, and platelets can regulate thrombus formation and modulate the coagulation process. Now that the key molecular players of coagulation and platelet activation have become clear, and their complex interactions with the vessel wall have been mapped out, we can also better speculate on the causes of thrombosis-related angiopathies.

摘要

止血包括血液凝固、血小板激活和血管修复等受到严格调控的过程。在受伤后,止血系统会激活大量血管和血管外受体,与血液成分协同作用,封闭对血管和周围组织造成的损伤。有助于止血的第一个重要组成部分是凝血系统,而第二个重要组成部分则始于血小板激活,血小板激活不仅有助于止血栓的形成,还有助于加速凝血系统。最终,凝血和血小板激活会被血液中的抑制剂和蛋白水解反馈环关闭。这篇综述总结了调节凝血和抗凝的蛋白酶激活的新概念,从而引发短暂的凝血酶生成和纤维蛋白凝块形成。它进一步推测了在这些蛋白酶作用下,血管内和血管外受体的(病理)生理作用。此外,这篇综述为理解内皮细胞、白细胞和血小板之间的信号和黏附相互作用如何调节血栓形成和调节凝血过程提供了一个新的框架。既然凝血和血小板激活的关键分子已经明确,并且它们与血管壁的复杂相互作用也已经被描绘出来,我们也可以更好地推测与血栓相关的血管病变的原因。

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