一种简便、无损的红血球浓缩物颗粒分离方法的研制。

Journal of extracellular biology Pub Date : 2025-01-17 eCollection Date: 2025-01-01 DOI:10.1002/jex2.70028
Marine Ghodsi, Anne-Sophie Cloos, Anaïs Lotens, Marine De Bueger, Patrick Van Der Smissen, Patrick Henriet, Nicolas Cellier, Christophe E Pierreux, Tomé Najdovski, Donatienne Tyteca
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引用次数: 0

摘要

红细胞浓缩物中的细胞外囊泡释放反映了积存病变的渐进性积累,可以作为血液中心除溶血外常规实施的一种新措施。然而,目前还没有标准化的隔离方案。在之前的一篇文章中,我们开发了一种可重复的基于超离心的方案(20,000 × g方案),该方案允许根据红细胞的囊泡水平将红细胞浓缩物分为三组。由于该方案不能满足常规要求,本研究的目标是开发一种更简单的方法,该方法基于低速离心(2000 × g方案)和有限的红细胞浓缩物体积,以匹配来自质量控制采样管的非破坏性采样。尽管存在主要以白蛋白和脂蛋白形式存在的污染物,但用2000 × g方案分离的材料含有红血球衍生的囊泡结构。它具有可重复性,可以预测20,000 × g方案获得的细胞外囊泡的数量,并且在6周的法定有效期内比溶血更好地区分三个囊泡队列。然而,通过减少红细胞浓缩物体积以适应质控管的体积,颗粒产率大大降低。因此,调整了离心时间和相对离心力(1000 × g协议),允许在不同时间的不同泡泡队列中,从主单元采样的大小体积之间恢复相似的颗粒数量和组成。在质量控制管和母袋中取样的小体积样品之间,用1000 × g协议进行了类似的观察。总之,我们的研究为使用2000 × g协议(适用于带有质量控制采样管的1000 × g协议)在血液中心进行颗粒测量铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of an easy non-destructive particle isolation protocol for quality control of red blood cell concentrates.

The extracellular vesicle release in red blood cell concentrates reflects progressive accumulation of storage lesions and could represent a new measure to be implemented routinely in blood centres in addition to haemolysis. Nevertheless, there is currently no standardized isolation protocol. In a previous publication, we developed a reproducible ultracentrifugation-based protocol (20,000 × g protocol) that allows to classify red blood cell concentrates into three cohorts according to their vesiculation level. Since this protocol was not adapted to meet routine requirements, the goal of this study was to develop an easier method based on low-speed centrifugation (2,000 × g protocol) and limited red blood cell concentrate volumes to match with a non-destructive sampling from the quality control sampling tubing. Despite the presence of contaminants, mainly in the form of albumin and lipoproteins, the material isolated with the 2,000 × g protocol contained red blood cell-derived vesicular structures. It was reproducible, could predict the number of extracellular vesicles obtained with the 20,000 × g protocol and better discriminated between the three vesiculation cohorts than haemolysis at the legal expiry date of 6 weeks. However, by decreasing red blood cell concentrate volumes to fit with the volume in the quality control tubing, particle yield was highly reduced. Therefore, centrifugation time and relative centrifugal force were adapted (1,000 × g protocol), allowing for the recovery of a similar particle number and composition between small and large volumes sampled from the main unit, in different vesiculation cohorts over time. A similar observation was made with the 1,000 × g protocol between small volumes sampled from the quality control tubing and the mother-bag. In conclusion, our study paves the way for the use of the 2,000 × g protocol (adapted to a 1,000 × g protocol with the quality control sampling tubing) for particle measurement in blood centres.

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