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
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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