Au Amanda E, Josefsson Emma C
a The Walter and Eliza Hall Institute of Medical Research, Cancer & Haematology Division , 1G Royal Parade, Melbourne , Australia.
b Department of Medical Biology , The University of Melbourne , Melbourne , Australia.
Platelets. 2017 Jun;28(4):342-353. doi: 10.1080/09537104.2016.1203401. Epub 2016 Aug 5.
Extracellular proteolysis of platelet plasma membrane proteins is an event that ensues platelet activation. Shedding of surface receptors such as glycoprotein (GP) Ibα, GPV and GPVI as well as externalized proteins P-selectin and CD40L releases soluble ectodomain fragments that are subsequently detectable in plasma. This results in the irreversible functional downregulation of platelet receptor-mediated adhesive interactions and the generation of biologically active fragments. In this review, we describe molecular insights into the regulation of platelet receptor and ligand shedding in health and disease. The scope of this review is specially focused on GPIbα, GPV, GPVI, P-selectin and CD40L where we: (1) describe the basic physiological regulation of expression and shedding of these proteins in hemostasis illustrate alterations in receptor expression during (2) apoptosis and (3) ex vivo storage relevant for blood banking purposes; (4) discuss considerations to be made when analyzing and interpreting shedding of platelet membrane proteins and finally; (5) collate clinical evidence that quantify these platelet proteins during disease.
血小板质膜蛋白的细胞外蛋白水解是血小板激活后发生的一个事件。糖蛋白(GP)Ibα、GPV和GPVI等表面受体以及外化蛋白P-选择素和CD40L的脱落会释放可溶性胞外域片段,随后可在血浆中检测到。这导致血小板受体介导的黏附相互作用发生不可逆的功能下调,并产生生物活性片段。在本综述中,我们描述了在健康和疾病状态下血小板受体和配体脱落调控的分子见解。本综述的范围特别聚焦于GPIbα、GPV、GPVI、P-选择素和CD40L,我们在其中:(1)描述这些蛋白质在止血过程中表达和脱落的基本生理调控;(2)说明细胞凋亡期间受体表达的变化;(3)阐述与血库目的相关的体外储存过程中的变化;(4)讨论分析和解释血小板膜蛋白脱落时应考虑的因素;最后(5)整理在疾病期间对这些血小板蛋白进行定量的临床证据。