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血小板通过抑制巨噬细胞依赖的炎症反应来保护机体免受感染性休克的影响,这种作用是通过环氧化酶 1 信号通路实现的。

Platelets protect from septic shock by inhibiting macrophage-dependent inflammation via the cyclooxygenase 1 signalling pathway.

机构信息

Division of Cardiovascular Medicine, Department of Internal Medicine, Saha Cardiovascular Center, University of Kentucky, Lexington, Kentucky 40536, USA.

出版信息

Nat Commun. 2013;4:2657. doi: 10.1038/ncomms3657.

Abstract

Although it has long been known that patients with sepsis often have thrombocytopenia and that septic patients with severe thrombocytopenia have a poor prognosis and higher mortality, the role of platelets in the pathogenesis of sepsis is poorly understood. Here we report a protective role of platelets in septic shock. We show that experimental thrombocytopenia induced by intraperitoneal injection of an anti-glycoprotein Ibα monoclonal antibody increases mortality and aggravates organ failure, whereas transfusion of platelets reduces mortality in lipopolysaccharide-induced endotoxemia and a bacterial infusion mouse sepsis model. Plasma concentrations of proinflammatory cytokines TNF-α and IL-6 are elevated by thrombocytopenia and decreased by platelet transfusion in septic mice. Furthermore, we identify that platelets protect from septic shock by inhibiting macrophage-dependent inflammation via the COX1/PGE₂/EP4-dependent pathway. Thus, these findings demonstrate a previously unappreciated role for platelets in septic shock and suggest that platelet transfusion may be effective in treating severely septic patients.

摘要

虽然人们早就知道败血症患者常伴有血小板减少症,而且严重血小板减少症的败血症患者预后不良、死亡率更高,但血小板在败血症发病机制中的作用仍不清楚。在这里,我们报告了血小板在感染性休克中的保护作用。我们发现,通过腹腔注射抗糖蛋白 Ibα 单克隆抗体诱导的实验性血小板减少症会增加死亡率并加重器官衰竭,而血小板输注则可降低脂多糖诱导的内毒素血症和细菌输注小鼠败血症模型中的死亡率。在感染性休克的小鼠中,血小板减少症会升高促炎细胞因子 TNF-α 和 IL-6 的血浆浓度,而血小板输注则会降低其浓度。此外,我们发现血小板通过 COX1/PGE₂/EP4 依赖性途径抑制巨噬细胞依赖性炎症,从而起到保护作用。因此,这些发现表明血小板在感染性休克中具有以前未被认识的作用,并提示血小板输注可能对治疗严重感染性休克的患者有效。

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