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Sickle cell disease biochip: a functional red blood cell adhesion assay for monitoring sickle cell disease

机译:镰状细胞病生物芯片:用于监测镰状细胞病的功能性红细胞粘附测定

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摘要

Sickle cell disease (SCD) afflicts millions of people worldwide and is associated with considerable morbidity and mortality. Chronic and acute vaso-occlusion are the clinical hallmarks of SCD and can result in pain crisis, widespread organ damage, and early movtality. Even though the molecular underpinnings of SCD were identified more than 60 years ago, there are no molecular or biophysical markers of disease severity that are feasibly measured in the clinic. Abnormal cellular adhesion to vascular endothelium is at the root of vaso-occlusion. However, cellular adhesion is not currently evaluated clinically. Here, we present a clinically applicable microfluidic device (SCD biochip) that allows serial quantitative evaluation of red blood cell (RBC) adhesion to endothelium-associated protein immobilized microchannels, in a closed and preprocessing-free system. With the SCD biochip, we have analyzed blood samples from more than 100 subjects and have shown associations between the measured RBC adhesion to endothelium associated proteins (fibronectin and laminin) and individual RBC characteristics, including hemoglobin content, fetal hemoglobin concentration, plasma lactate dehydrogenase level, and reticulocyte count. The SCD biochip is a functional adhesion assay, reflecting quantitative evaluation of RBC adhesion, which could be used at baseline, during crises, relative to various long-term complications, and before and after therapeutic interventions.
机译:镰状细胞病(SCD)困扰着全球数百万人,并与相当高的发病率和死亡率有关。慢性和急性血管闭塞是SCD的临床标志,可导致疼痛危机,广泛的器官损伤和早期活动。尽管SCD的分子基础已在60年前被发现,但尚无可在临床上测量出的疾病严重程度的分子或生物物理标志物。细胞对血管内皮的异常粘附是血管闭塞的根源。但是,目前尚无临床评估细胞粘附的方法。在这里,我们介绍了一种临床适用的微流控设备(SCD生物芯片),它允许在封闭且无预处理的系统中对红细胞(RBC)对与内皮相关蛋白固定的微通道的粘附进行系列定量评估。使用SCD生物芯片,我们分析了100多个受试者的血液样本,并显示了测量的RBC对内皮相关蛋白(纤连蛋白和层粘连蛋白)的粘附力与单个RBC特性之间的关联,包括血红蛋白含量,胎儿血红蛋白浓度,血浆乳酸脱氢酶水平和网状细胞计数。 SCD生物芯片是一种功能性粘附测定,反映了RBC粘附的定量评估,可用于基线,危机期间,相对于各种长期并发症以及治疗干预前后。

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