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循环微泡在骨髓增生异常综合征中促凝作用较弱且携带不同的微小RNA。

Circulating microvesicles are less procoagulant and carry different miRNA cargo in myelodysplasia.

作者信息

Enjeti Anoop K, Ariyarajah Anita, D'Crus Angel, Riveros Carlos, Seldon Michael, Lincz Lisa F

机构信息

Haematology Department, Calvary Mater Newcastle, Australia; School of Medicine and Public Health, University of Newcastle, Australia; Pathology North-Hunter, NSW, Australia; Hunter Medical Research Institute, New Lambton, Australia; Hunter Cancer Research Alliance, NSW, Australia.

Haematology Department, Calvary Mater Newcastle, Australia.

出版信息

Blood Cells Mol Dis. 2019 Feb;74:37-43. doi: 10.1016/j.bcmd.2018.11.001. Epub 2018 Nov 7.

DOI:10.1016/j.bcmd.2018.11.001
PMID:30454964
Abstract

BACKGROUND AND AIMS

Myelodysplasia (MDS) is characterised by abnormal haematopoiesis and increased risk of bleeding. Microvesicles (MV) play a key role in coagulation and their impact in MDS is unknown.

METHODS

Platelet free plasma from 35 red-cell transfusion-dependent MDS patients and 15 controls were analysed. Pro-coagulant function was assessed by the XaCT assay and by thrombin generation (ETP). Total MV were enumerated by nano-tracking analysis. MV subsets were quantified by flow cytometry after staining with specific antibodies for various endovascular cell types. Small RNA was quantitated and sequenced. The MV measurements were correlated with MDS clinical risk scores and level of transfusion dependence.

RESULTS

The pro-coagulant function of MV was significantly lower in MDS. All the MV subtypes, as measured by flow cytometric markers, were also significantly lower. The small RNA and miRNA cargo were significantly higher in MDS. The miRNA profile showed that mir-28 and mir-LETD7 were under expressed whilst mir-584J and mir-4485 were over expressed in MV from MDS.

CONCLUSIONS

Circulating MV in MDS show reduced pro-coagulant functional activity, reduced subtypes by flow cytometry and significantly different miRNA content. However, the levels or subtypes of MV did not predict the clinical phenotype or level of transfusion dependence.

摘要

背景与目的

骨髓增生异常综合征(MDS)的特征是造血异常和出血风险增加。微泡(MV)在凝血过程中起关键作用,但其在MDS中的影响尚不清楚。

方法

分析了35例依赖红细胞输血的MDS患者和15例对照者的无血小板血浆。通过XaCT试验和凝血酶生成(ETP)评估促凝血功能。通过纳米跟踪分析对总MV进行计数。在用针对各种血管内皮细胞类型的特异性抗体染色后,通过流式细胞术对MV亚群进行定量。对小RNA进行定量和测序。将MV测量结果与MDS临床风险评分和输血依赖程度相关联。

结果

MDS中MV的促凝血功能显著降低。通过流式细胞术标记物测量的所有MV亚型也显著降低。MDS中的小RNA和miRNA含量显著更高。miRNA谱显示,在MDS的MV中,mir-28和mir-LETD7表达不足,而mir-584J和mir-4485表达过度。

结论

MDS中的循环MV显示促凝血功能活性降低,流式细胞术检测的亚型减少,且miRNA含量存在显著差异。然而,MV的水平或亚型并不能预测临床表型或输血依赖程度。

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