The source of HLA molecules on platelets: Does platelets adsorb soluble HLA molecules from their environment?

IF 0.4 Q4 PEDIATRICS
T. Dargahi, F. Yari, N. Rezaei
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引用次数: 0

Abstract

Background: The origin and function of human leukocyte antigen (HLA) class I molecules on platelets are still highly arguable. Given the differences in the results of the previous studies in this regard, the lack of research in recent years, and the clinical importance of HLA class I molecules, the absorption capacity of platelets for soluble HLA class I molecules was studied in this investigation. Materials and Methods: In this experimental study, HLA-A2 antigen was purified from a B cell precursor leukemia cell line (Nalm-6) by cell membrane protein solubilization and usage of HLA-A2 affinity column. Platelet concentrates (PCs) were received from Tehran Blood Transfusion Center. Eighteen bags of HLA-A2-negative PCs were prepared randomly and treated with various concentrations of the purified HLA antigen (100, 500, and 1000 ng/ml) for 48 to 72 hours. Subsequently, the HLA-A2 levels were evaluated on platelets by flow cytometery technique. Data were evaluated using repeated measure ANOVA.P-values less than 0.05 were considered significant. Results: The results of this study showed that the purified protein was an HLA molecule (HLA-A2).  After the treatment of platelets and HLA molecules, platelets inability was shown for the attracting of HLA molecules. This finding was true in both media of RPMI and plasma. The differences between the case (HLA-treated platelets) and control (untreated platelets) were not significant (p-values> 0.05). Conclusion: Platelets were unable to significantly adsorb exogenous HLA antigens from their environment. Further studies are needed to unravel the nature and origin of HLA molecules on platelets.
HLA分子在血小板上的来源:血小板是否从其环境中吸附可溶性HLA分子?
背景:人类白细胞抗原(HLA) I类分子在血小板上的起源和功能仍然有很大的争议。鉴于以往在这方面的研究结果存在差异,加之近年来研究的缺失,以及HLA I类分子在临床中的重要性,本研究对血小板对可溶性HLA I类分子的吸收能力进行了研究。材料与方法:本实验采用细胞膜蛋白增溶法,利用HLA-A2亲和柱,从B细胞前体白血病细胞株(Nalm-6)中纯化HLA-A2抗原。从德黑兰输血中心收到血小板浓缩物(PCs)。随机制备HLA- a2阴性PCs 18袋,分别用不同浓度纯化HLA抗原(100、500、1000 ng/ml)处理48 ~ 72小时。随后,用流式细胞术评估血小板HLA-A2水平。采用重复测量方差分析对数据进行评价。p值小于0.05被认为是显著的。结果:本研究结果表明,纯化蛋白为HLA- a2分子。经血小板和HLA分子处理后,显示血小板无法吸引HLA分子。这一发现在RPMI和血浆介质中都是正确的。病例组(hla处理过的血小板)与对照组(未处理过的血小板)的差异无统计学意义(p值0.05)。结论:血小板不能明显吸附环境中的外源HLA抗原。需要进一步的研究来揭示血小板上HLA分子的性质和起源。
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来源期刊
CiteScore
0.80
自引率
33.30%
发文量
33
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