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使用 microRNA 开关和磁激活细胞分选大规模纯化人诱导多能干细胞衍生细胞。

Purification of human iPSC-derived cells at large scale using microRNA switch and magnetic-activated cell sorting.

机构信息

Center for iPS Cell Research and Application, Kyoto University, Kyoto 606-8507, Japan; Department of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Center for iPS Cell Research and Application, Kyoto University, Kyoto 606-8507, Japan.

出版信息

Stem Cell Reports. 2022 Jul 12;17(7):1772-1785. doi: 10.1016/j.stemcr.2022.05.003. Epub 2022 Jun 9.

Abstract

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.

摘要

对于使用多能干细胞 (PSC) 衍生细胞的再生细胞疗法,需要大量纯化的细胞。磁激活细胞分选 (MACS) 是一种收集靶抗原阳性细胞的有效方法;然而,在不使用针对所需细胞类型的抗体的情况下,高效地大规模纯化各种细胞类型仍然是一个挑战。在这里,我们开发了一种将 microRNA (miRNA) 反应性 mRNA 开关 (miR-switch) 与 MACS 结合的技术 (miR-switch-MACS),以快速有效地纯化大量 PSC 衍生细胞。我们设计了 miR-switches,以检测靶细胞中表达的特定 miRNAs,并控制 CD4 编码转基因的翻译,作为 MACS 的选择标记。为了大规模纯化诱导的 PSC 衍生心肌细胞 (iPSC-CMs),我们转导了 miR-208a-CD4 开关-MACS,并有效地获得了纯化的 iPSC-CMs。此外,miR-375-CD4 开关-MACS 高度纯化了表达嗜铬粒蛋白 A 的胰腺胰岛素产生细胞及其祖细胞。总的来说,miR-switch-MACS 方法可有效地纯化用于细胞替代治疗的靶 PSC 衍生细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f10/9287667/5cb12221a956/fx1.jpg

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