Division of Hematology and Transfusion Medicine, Lund University, Lund, Sweden.
Sanquin Research, Department of Experimental Immunohematology, Landsteiner Laboratory, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Transfus Med Rev. 2020 Oct;34(4):209-220. doi: 10.1016/j.tmrv.2020.09.005. Epub 2020 Sep 19.
Platelets are the primary cellular mediators of hemostasis and this function firmly acquaints them with a variety of inflammatory processes. For example, platelets can act as circulating sentinels by expressing Toll-like receptors (TLR) that bind pathogens and this allows platelets to effectively kill them or present them to cells of the immune system. Furthermore, activated platelets secrete and express many pro- and anti-inflammatory molecules that attract and capture circulating leukocytes and direct them to inflamed tissues. In addition, platelets can directly influence adaptive immune responses via secretion of, for example, CD40 and CD40L molecules. Platelets are also the source of most of the microvesicles in the circulation and these miniscule elements further enhance the platelet's ability to communicate with the immune system. More recently, it has been demonstrated that platelets and their parent cells, the megakaryocytes (MK), can also uptake, process and present both foreign and self-antigens to CD8+ T-cells conferring on them the ability to directly alter adaptive immune responses. This review will highlight several of the non-hemostatic attributes of platelets that clearly and rightfully place them as integral players in immune reactions.
血小板是止血的主要细胞介质,这一功能使它们与各种炎症过程紧密相关。例如,血小板可以通过表达 Toll 样受体 (TLR) 来充当循环中的哨兵,这些受体可以与病原体结合,从而使血小板能够有效地杀死它们或将其呈现给免疫系统的细胞。此外,激活的血小板会分泌和表达许多促炎和抗炎分子,这些分子可以吸引并捕获循环中的白细胞,并将其引导至炎症组织。此外,血小板还可以通过分泌例如 CD40 和 CD40L 分子来直接影响适应性免疫反应。血小板也是循环中大多数微泡的来源,这些微小的元素进一步增强了血小板与免疫系统进行通信的能力。最近,已经证明血小板及其母细胞巨核细胞 (MK) 也可以摄取、加工和呈现外来和自身抗原给 CD8+ T 细胞,赋予它们直接改变适应性免疫反应的能力。这篇综述将重点介绍血小板的几种非止血特性,这些特性明确地将它们置于免疫反应的重要参与者地位。