Exosomes Produced from 3D Cultures of MSCs by Tangential Flow Filtration Show Higher Yield and Improved Activity

微泡 间充质干细胞 外体 微载波 细胞生物学 干细胞 胞外囊泡 纳米粒子跟踪分析 细胞培养 微泡 化学 体外 细胞外小泡 生物 生物物理学 小RNA 生物化学 基因 遗传学
作者
Reka A. Haraszti,Rachael Miller,Matteo Stoppato,Yves Y. Sere,Andrew H. Coles,Marie-Cécile Didiot,Rachel Wollacott,Ellen Sapp,Michelle L. Dubuke,Xuni Li,Scott A. Shaffer,Marian DiFiglia,Xiawei Wei,Neil Aronin,Anastasia Khvorova
出处
期刊:Molecular Therapy [Elsevier BV]
卷期号:26 (12): 2838-2847 被引量:274
标识
DOI:10.1016/j.ymthe.2018.09.015
摘要

Exosomes can deliver therapeutic RNAs to neurons. The composition and the safety profile of exosomes depend on the type of the exosome-producing cell. Mesenchymal stem cells are considered to be an attractive cell type for therapeutic exosome production. However, scalable methods to isolate and manufacture exosomes from mesenchymal stem cells are lacking, a limitation to the clinical translation of exosome technology. We evaluate mesenchymal stem cells from different sources and find that umbilical cord-derived mesenchymal stem cells produce the highest exosome yield. To optimize exosome production, we cultivate umbilical cord-derived mesenchymal stem cells in scalable microcarrier-based three-dimensional (3D) cultures. In combination with the conventional differential ultracentrifugation, 3D culture yields 20-fold more exosomes (3D-UC-exosomes) than two-dimensional cultures (2D-UC-exosomes). Tangential flow filtration (TFF) in combination with 3D mesenchymal stem cell cultures further improves the yield of exosomes (3D-TFF-exosomes) 7-fold over 3D-UC-exosomes. 3D-TFF-exosomes are seven times more potent in small interfering RNA (siRNA) transfer to neurons compared with 2D-UC-exosomes. Microcarrier-based 3D culture and TFF allow scalable production of biologically active exosomes from mesenchymal stem cells. These findings lift a major roadblock for the clinical utility of mesenchymal stem cell exosomes.
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