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PMID: 28960897 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

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

Biotechnology progress ·Vol. 33 ·No. 6 ·2017-00-00 ·页码 1614-1629

Martinez AF, McMahon RD, Horner M, Miller WM

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.

Keywords
CFD cell therapies megakaryocytes microfluidic bioreactor platelets
MeSH 主题词
Bioreactors Blood Platelets/chemistry,metabolism Cells, Cultured Computational Biology Humans Hydrodynamics Megakaryocytes/metabolism Microfluidics/methods Platelet Transfusion Shear Strength
作者与单位
共 4 位作者,点击展开单位 / ORCID
Martinez Andres F
Dept. of Chemical and Biological Engineering, Northwestern University, Evanston, IL, 60208.
McMahon Richard D
Master of Biotechnology Program, Northwestern University, Evanston, IL, 60208.
Horner Marc
ANSYS, Inc., Evanston, IL, 60201.
Miller William M ORCID
Dept. of Chemical and Biological Engineering, Master of Biotechnology Program, Northwestern University, Evanston, IL, 60208.
Article Info
Journal
Biotechnology progress
Abbr.
Biotechnol Prog
ISSN
1520-6033
Published
2017-00-00
电子出版
2017-00-13
页码
1614-1629
Language
English
Country/Region
United States
NLM ID
8506292
基金资助
NHLBI NIH HHS · R01 HL130760 · United States
NIGMS NIH HHS · T32 GM008449 · United States
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