首页> 外文期刊>PLoS One >P38 mitogen activated protein kinase inhibitor improves platelet in vitro parameters and in vivo survival in a SCID mouse model of transfusion for platelets stored at cold or temperature cycled conditions for 14 days
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P38 mitogen activated protein kinase inhibitor improves platelet in vitro parameters and in vivo survival in a SCID mouse model of transfusion for platelets stored at cold or temperature cycled conditions for 14 days

机译:P38丝裂原激活蛋白激酶抑制剂改善了血小板体外参数,体内存活中的SCID小鼠输血模型,用于储存在寒冷或温度循环条件下的血小板14天

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Platelets for transfusion are stored at room temperature (20–24°C) up to 7 days but decline in biochemical and morphological parameters during storage and can support bacterial proliferation. This decline is reduced with p38MAPK inhibitor, VX-702. Storage of platelets in the cold (4–6°C) can reduce bacterial proliferation but platelets get activated and have reduced circulation when transfused. Thermocycling (cold storage with brief periodic warm ups) reduces some of the effects of cold storage. We evaluated in vitro properties and in vivo circulation in SCID mouse model of human platelet transfusion of platelets stored in cold or thermocycled for 14 days with and without VX-702. Apheresis platelet units (N = 15) were each aliquoted into five storage bags and stored under different conditions: room temperature; cold temperature; thermocycled temperature; cold temperature with VX-702; thermocycled temperature with VX-702. Platelet in vitro parameters were evaluated at 1, 7 and 14 days. On day 14, platelets were infused into SCID mice to assess their retention in circulation by flow cytometry. VX-702 reduced negative platelet parameters associated with cold and thermocycled storage such as an increase in expression of activation markers CD62, CD63 and of phosphatidylserine (marker of apoptosis measured by Annexin binding) and lowered the rise in lactate (marker of increase in anaerobic metabolism). However, VX-702 did not inhibit agonist-induced platelet aggregation indicating that it does not interfere with platelet hemostatic function. In vivo, VX-702 improved initial recovery and area under the curve in circulation of human platelets infused into a mouse model that has been previously validated against a human platelet infusion clinical trial. In conclusion, inhibition of p38MAPK during 14-days platelet storage in cold or thermocycling conditions improved in vitro platelet parameters and platelet circulation in the mouse model indicating that VX-702 may improve cell physiology and clinical performance of human platelets stored in cold conditions.
机译:输血的血小板在室温(20-24°C)上储存,最多7天,但储存过程中的生化和形态学参数下降,并且可以支持细菌增殖。使用P38MAPK抑制剂VX-702降低了这种下降。在寒冷(4-6°C)中血小板储存可以降低细菌增殖,但血小板被激活并在输出时减少循环。热循环(带有短暂的定期预热的冷库)减少了冷库的一些影响。我们在体外性质和体内循环进行了分类,SCID小鼠模型中的人血小板输注血小板的血小板输注,储存在冷或热循环14天,无VX-702。将血小板单位(n = 15)各自等分为五个储存袋并在不同的条件下储存:室温;寒冷;热循环温度; VX-702的寒冷温度;具有VX-702的热循环温度。在1,7和14天内评估血小板体外参数。在第14天,将血小板注入SCID小鼠以评估流式细胞术循环的保留。 Vx-702减少了与冷和热循环储存相关的负血小板参数,例如激活标记CD62,CD63和磷脂酰丝氨酸的表达的增加(通过膜蛋白结合测量的细胞凋亡的标志物),降低了乳酸的升高(厌氧代谢增加的标志物增加)。然而,VX-702没有抑制激动剂诱导的血小板聚集,表明它不会干扰血小板止血功能。在体内,VX-702改善了曲线下的初始恢复和面积,以预先对人类血小板输注临床试验验证的鼠标模型的人血小板循环。总之,抑制了在冷或热环循环条件下的血小板储存期间P38MAPK的抑制改善了小鼠模型中的体外血小板参数和血小板循环,表明VX-702可以改善储存在寒冷条件下的人血小板的细胞生理学和临床表现。

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