生物
单元格排序
小RNA
诱导多能干细胞
细胞生物学
电池类型
免疫磁选
细胞
分子生物学
祖细胞
转染
计算生物学
干细胞
细胞培养
流式细胞术
胚胎干细胞
遗传学
基因
作者
Yuta Tsujisaka,Takeshi Hatani,Chikako Okubo,Ryô Itô,Azuma Kimura,Megumi Narita,Kazuhisa Chonabayashi,Shunsuke Funakoshi,Antonio Lucena-Cacace,Tarō Toyoda,Kenji Osafune,Takeshi Kimura,Hirohide Saito,Yoshinori Yoshida
标识
DOI:10.1016/j.stemcr.2022.05.003
摘要
For regenerative cell therapies using pluripotent stem cell (PSC)-derived cells, large quantities of purified cells are required. Magnetic-activated cell sorting (MACS) is a powerful approach to collect target antigen-positive cells; however, it remains a challenge to purify various cell types efficiently at large scale without using antibodies specific to the desired cell type. Here we develop a technology that combines microRNA (miRNA)-responsive mRNA switch (miR-switch) with MACS (miR-switch-MACS) to purify large amounts of PSC-derived cells rapidly and effectively. We designed miR-switches that detect specific miRNAs expressed in target cells and controlled the translation of a CD4-coding transgene as a selection marker for MACS. For the large-scale purification of induced PSC-derived cardiomyocytes (iPSC-CMs), we transferred miR-208a-CD4 switch-MACS and obtained purified iPSC-CMs efficiently. Moreover, miR-375-CD4 switch-MACS highly purified pancreatic insulin-producing cells and their progenitors expressing Chromogranin A. Overall, the miR-switch-MACS method can efficiently purify target PSC-derived cells for cell replacement therapy.
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