供体池大小对再生医学中血小板裂解液来源的细胞外囊泡变异性的影响。

Extracellular vesicles and circulating nucleic acids Pub Date : 2024-05-29 eCollection Date: 2024-01-01 DOI:10.20517/evcna.2024.05
Andreu Miquel Amengual-Tugores, Carmen Ráez-Meseguer, Maria Antònia Forteza-Genestra, Javier Calvo, Antoni Gayà, Marta Monjo, Joana Maria Ramis
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引用次数: 0

摘要

目的:本研究的目的是通过伤口愈合试验,确定血小板裂解液衍生的细胞外囊泡(pEV)在从血小板浓缩物(PC,来自5个供体)或多个血小板浓缩物(MPC,即50个供体)中分离时的特征和功能的变异性。方法:在类似gmp的条件下,在洁净室采用排色色谱(SEC)分离pEV。通过蛋白质浓度、纳米颗粒跟踪分析(NTA)、透射电子显微镜(TEM)和使用MACSPlex™阵列进行EV表面分析的流式细胞术来评估从PC (PC-EV)或MPC (MPC-EV)获得的pEV之间的差异特征。在细胞培养中,通过代谢活性和LDH活性测定以及处理24小时后的伤口愈合试验来确定分离的pEV的功能。结果:无论是从PC分离还是从MPC分离,pEV特征评估均无显著差异。在功能方面,从PC(5个供体)分离的pEV池获得了更高的伤口愈合百分比。在比较来自PC(5名供者)或MPC(50名供者)的pEV的所有评估变量时,没有发现变异系数(CV)的差异。结论:我们的研究结果表明,在MPC-EV和PC-EV的分析变量中没有显著差异,挑战了更大的pEV分离供体池的必要性。值得注意的是,我们的结果表明,与血小板浓缩物不同,不需要大量供体来降低pEV的变异性,这表明仅5个供体就可以提供一致和可靠的治疗产品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of donor pool size on the variability of platelet lysate-derived extracellular vesicles for regenerative medicine.

Aim: The objective of the present study was to determine the variability of platelet lysate-derived extracellular vesicles (pEV), in terms of characteristics and functionality through wound healing assays, when isolated either from platelet concentrates (PC, obtained from 5 donors) or from multiple PC (MPC, that is 50 donors). Methods: pEV were isolated under GMP-like conditions in a clean room using Size Exclusion Chromatography (SEC). The differential characteristics between pEV obtained from PC (PC-EV) or MPC (MPC-EV) were evaluated by means of protein concentration, Nanoparticle Tracking Analysis (NTA), Transmission Electron Microscopy (TEM), and flow cytometry using the MACSPlex™ arrays for surface analysis profiling of EV. The functionality of the isolated pEV was determined in cell culture by metabolic activity and LDH activity determination and through a wound healing assay after 24 h treatment. Results: No significant differences were observed in the pEV characteristics evaluated, whether isolated from PC or MPC. As regards functionality, a higher wound closure percentage was obtained in those pEV pools isolated from PC (5 donors). No differences in the coefficient of variation (CV) were found when comparing all the evaluated variables of pEV derived either from PC (5 donors) or from MPC (50 donors). Conclusion: Our findings challenge the necessity of a larger donor pool for pEV isolation, revealing no significant variations in the analyzed variables of MPC-EV and PC-EV. Notably, our results suggest that, unlike platelet concentrates, a high number of donors is not required to reduce the variability of pEV, showing that the pool of only 5 donors can provide a consistent and reliable therapeutic product.

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