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血小板活化过程中α-颗粒内容物的释放。

Release of α-granule contents during platelet activation.

作者信息

Smith Christopher W

机构信息

Institute of Cardiovascular Sciences, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, B15 2TT, Birmingham, UK.

出版信息

Platelets. 2022 May 19;33(4):491-502. doi: 10.1080/09537104.2021.1913576. Epub 2021 Sep 25.

Abstract

Upon activation, platelets release a plethora of factors which help to mediate their dynamic functions in hemostasis, inflammation, wound healing, tumor metastasis and angiogenesis. The majority of these bioactive molecules are released from α-granules, which are unique to platelets, and contain an incredibly diverse repertoire of cargo including; integral membrane proteins, pro-coagulant molecules, chemokines, mitogenic, growth and angiogenic factors, adhesion proteins, and microbicidal proteins. Clinically, activation of circulating platelets has increasingly been associated with various disease states. Biomarkers indicating the level of platelet activation in patients can therefore be useful tools to evaluate risk factors to predict future complications and determine treatment strategies or evaluate antiplatelet therapy. The irreversible nature of α-granule secretion makes it ideally suited as a marker of platelet activation. This review outlines the release and contents of platelet α-granules, as well as the membrane bound, and soluble α-granule cargo proteins that can be used as biomarkers of platelet activation.

摘要

激活后,血小板会释放大量因子,这些因子有助于介导其在止血、炎症、伤口愈合、肿瘤转移和血管生成中的动态功能。这些生物活性分子大多从α-颗粒释放,α-颗粒是血小板特有的,包含种类极其多样的货物,包括:整合膜蛋白、促凝血分子、趋化因子、有丝分裂原、生长和血管生成因子、黏附蛋白以及杀菌蛋白。临床上,循环血小板的激活越来越多地与各种疾病状态相关。因此,指示患者血小板激活水平的生物标志物可作为评估风险因素以预测未来并发症、确定治疗策略或评估抗血小板治疗的有用工具。α-颗粒分泌的不可逆性使其非常适合作为血小板激活的标志物。本综述概述了血小板α-颗粒的释放和内容物,以及可作为血小板激活生物标志物的膜结合和可溶性α-颗粒货物蛋白。

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