Assessing the Vascular Deformability of Erythrocytes and Leukocytes: From Micropipettes to Microfluidics

M. Scott, K. Matthews, Hongshen Ma
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引用次数: 3

Abstract

Among the most crucial rheological characteristics of blood cells within the vasculature is their ability to undergo the shape change (i.e., deform). The signifi-cance of cellular deformability is readily apparent based solely on the disparate mean size of human erythrocytes (~8 μ m) and leukocytes (10–25 μ m) compared to the minimum luminal size of capillaries (4–5 μ m) and splenic interendothelial clefts (0.5–1.0 μ m) they must transit. Changes in the deformability of either cell will result in their premature mechanical clearance as well as an enhanced possibility of intravascular lysis. In this chapter, we will demonstrate how microfluidic devices can be used to examine the vascular deformability of erythrocytes and agranular leukocytes. Moreover, we will compare microfluidic assays with previous studies utilizing micropipettes, ektacytometry and micropore cell transit times. As will be discussed, microfluidics-based devices offer a low-cost, high throughput alternative to these previous, and now rather ancient, technologies.
评估红细胞和白细胞的血管变形能力:从微移液管到微流体
在脉管系统中,血细胞最重要的流变特性是它们能够经历形状变化(即变形)。细胞变形能力的重要性是显而易见的,仅仅基于人红细胞(~8 μ m)和白细胞(10-25 μ m)的平均大小与毛细血管(4-5 μ m)和脾内皮间裂隙(0.5-1.0 μ m)的最小管腔大小的不同。这两种细胞变形能力的改变将导致它们过早的机械清除,并增加血管内溶解的可能性。在本章中,我们将演示如何使用微流体装置来检查红细胞和颗粒白细胞的血管变形性。此外,我们将比较微流控分析与先前使用微移液管、分光光度法和微孔细胞传递时间的研究。正如将讨论的那样,基于微流体的设备提供了一种低成本,高通量的替代方案,以取代这些以前的,现在相当古老的技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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