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一种用于实时研究前血小板形成和快速释放血小板的均匀剪切速率微流控生物反应器。

A uniform-shear rate microfluidic bioreactor for real-time study of proplatelet formation and rapidly-released platelets.

作者信息

Martinez Andres F, McMahon Richard D, Horner Marc, Miller William M

机构信息

Dept. of Chemical and Biological Engineering, Northwestern University, Evanston, IL, 60208.

Master of Biotechnology Program, Northwestern University, Evanston, IL, 60208.

出版信息

Biotechnol Prog. 2017 Nov;33(6):1614-1629. doi: 10.1002/btpr.2563. Epub 2017 Oct 13.

DOI:10.1002/btpr.2563
PMID:28960897
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5745287/
Abstract

Platelet transfusions, with profound clinical importance in blood clotting and wound healing, are entirely derived from human volunteer donors. Hospitals rely on a steady supply of donations, but these methods are limited by a 5-day shelf life, the potential risk of contamination, and differences in donor/recipient histocompatibility. These challenges invite the opportunity to generate platelets ex vivo. Although much progress has been made in generating large numbers of culture-derived megakaryocytes (Mks, the precursor cells to platelets), stimulating a high percentage of Mks to undergo platelet release remains a major challenge. Recent studies have demonstrated the utility of shear forces to enhance platelet release from cultured Mks. In this study, we performed a computational fluid dynamics (CFD) analysis of several published platelet microbioreactor systems, and used the results to develop a new 7-µm slit bioreactor-with well-defined flow patterns and uniform shear profiles. This uniform-shear-rate bioreactor (USRB-7µm) permits real-time visualization of the proplatelet (proPLT) formation process and the rapid-release of individual platelet-like-particles (PLPs), which has been observed in vivo, but not previously reported for platelet bioreactors. We showed that modulating shear forces and flow patterns had an immediate and significant impact on PLP generation. Surprisingly, using a single flow instead of dual flows led to an unexpected six-fold increase in PLP production. By identifying particularly effective operating conditions within a physiologically relevant environment, this USRB-7µm will be a useful tool for the study and analysis of proPLT/PLP formation that will further understanding of how to increase ex vivo platelet release. © 2017 American Institute of Chemical Engineers Biotechnol. Prog., 33:1614-1629, 2017.

摘要

血小板输注在血液凝固和伤口愈合中具有极其重要的临床意义,其完全来源于人类志愿者捐赠者。医院依赖稳定的捐赠供应,但这些方法受到5天保质期、污染的潜在风险以及供体/受体组织相容性差异的限制。这些挑战促使人们有机会在体外生成血小板。尽管在生成大量培养来源的巨核细胞(Mks,血小板的前体细胞)方面已经取得了很大进展,但刺激高比例的Mks进行血小板释放仍然是一个重大挑战。最近的研究表明,剪切力有助于增强培养的Mks释放血小板。在本研究中,我们对几个已发表的血小板微生物反应器系统进行了计算流体动力学(CFD)分析,并利用结果开发了一种新的7微米狭缝生物反应器,其具有明确的流动模式和均匀的剪切分布。这种均匀剪切速率生物反应器(USRB-7μm)能够实时可视化前血小板(proPLT)的形成过程以及单个类血小板颗粒(PLP)的快速释放,这一现象在体内已被观察到,但此前在血小板生物反应器中尚未有报道。我们发现,调节剪切力和流动模式对PLP生成有直接且显著的影响。令人惊讶的是,使用单一流体而非双流体导致PLP产量意外增加了六倍。通过在生理相关环境中确定特别有效的操作条件,这种USRB-7μm将成为研究和分析proPLT/PLP形成的有用工具,有助于进一步了解如何增加体外血小板释放。©2017美国化学工程师学会生物技术进展,33:1614 - 1629,2017。

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