输血相关性急性肺损伤中血红素诱导的嗜中性粒细胞活化的自噬调节与microRNA表达相关

Ren-In You , Ching-Liang Ho , Ming-Shen Dai , Hsiu-Man Hung , Chu-Shun Chen , Tsu-Yi Chao
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引用次数: 2

摘要

输血相关性急性肺损伤(TRALI)是输血治疗后死亡的主要原因。TRALI的发病机制与肺中性粒细胞活化有关,引起内皮损伤和毛细血管渗漏,从而引起中性粒细胞外渗。血红素相关分子来源于红细胞的溶血成分,被认为是一种刺激物,在TRALI诱导中性粒细胞活化。为了研究TRALI中性粒细胞转录后的变化,我们在中性粒细胞中进行了血红素相关分子诱导的活性氧产生作为模型。从肝素化的外周血中分离中性粒细胞,用血红素相关分子刺激。刺激后,通过鲁米诺测定、流式细胞术和实时聚合酶链反应分析中性粒细胞的活性氧生成、脱颗粒、吞噬活性和miRNA表达谱。探讨了靶向NADPH氧化酶和自噬的miRNA在中性粒细胞活化TRALI中的表达。mirna的表达谱将是疾病严重程度和患者输血分级的有用预测因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Autophagy regulation in heme-induced neutrophil activation is associated with microRNA expression on transfusion-related acute lung injury

Transfusion-related acute lung injury (TRALI) is the leading cause of death after transfusion therapy. The pathogenesis of TRALI is associated with neutrophil activation in the lungs, causing endothelial damage and capillary leakage, and thus neutrophil extravasation. Heme-related molecules derived from the hemolysis of red blood cell components have been recognized as a stimulator, inducing neutrophil activation at TRALI. To investigate post-transcriptional changes of the neutrophil at TRALI, we performed heme-related molecules induced reactive oxygen species production in the neutrophil as a model. Neutrophils were isolated from heparinized peripheral blood and stimulated with heme-related molecules. After stimulation, reactive oxygen species production, degranulation, phagocytosis activity, and miRNA expression profile of neutrophil were analyzed by luminol assay, flow cytometry, and real-time polymerase chain reaction. The expression of miRNA targeting NADPH oxidase and autophagy in the neutrophil activation of TRALI was explored. The expression profile of miRNAs will be a useful predictor of disease severity and for the grading of patients for transfusion.

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