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作 者:杨玲玲[1] 石丽萍[1] 龚晓燕[1] 陈立[1] 任芙蓉[1]
机构地区:[1]北京市红十字血液中心安全输血室,100088
出 处:《北京医学》2015年第2期157-159,共3页Beijing Medical Journal
基 金:首都卫生发展科研专项(首发2011-1019-01)
摘 要:目的测定冷藏(4℃)保存48 h后血小板膜糖蛋白GPⅠbα末端糖基脱落情况。方法分别以一定浓度梯度的FITC-s WGA、FITC-RCA-1、FITC-ECA标记血小板,应用流式细胞仪检测,确定最佳工作浓度。检测冷藏保存48 h后血小板GPⅠbα末端唾液酸基及次末端半乳糖基脱落情况。结果 FITC-s WGA、FITC-RCA-1、FITC-ECA工作浓度分别为2μg/ml、2μg/ml、30μg/ml时标记效果好。冷藏保存48 h后GPⅠbα末端唾液酸基及次末端半乳糖基脱落较22℃常规保存明显增加,分别增至(156±18)%及(123±13)%,差异有统计学意义(P<0.01)。结论冷藏保存48 h可致血小板膜糖蛋白GPⅠbα末端糖基脱落增加。Objective To measure the exposed residues of platelet membrane glycoprotein GPⅠbαwith flow cy-tometry (FCM) after refrigerating 48 h. Methods A series of concentration was set, and the optimal working concentration of FITC-sWGA, FITC-RCA-1, FITC-ECA was determined respectively. The platelet membrane GPⅠbαterminal exposed residues were analyzed after 22℃ preservation and 4℃ refrigeration respectively. Results FITC-sWGA, FITC-RCA-1 and FITC-ECA worked well at 2μg/ml, 2μg/ml and 30μg/ml respectively. Refrigeration led to increasing of GPⅠbαterminal sugar radicals shedding, terminal sialic acid group shedding increased to (156±18)%(P〈0.01), and penultimate galactose group shedding increased to (123 ±13)%(P〈0.01). Conclusion Refrigerating platelets for 48 h leads to in-creasing of platelet GPⅠbαsubunit terminal sugar radicals shedding.
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