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MicroRNA-302 开关可识别并清除未分化的人类多能干细胞。

MicroRNA-302 switch to identify and eliminate undifferentiated human pluripotent stem cells.

机构信息

Department of Life Science Frontiers, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.

Department of Clinical Application, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.

出版信息

Sci Rep. 2016 Sep 9;6:32532. doi: 10.1038/srep32532.

Abstract

The efficiency of pluripotent stem cell differentiation is highly variable, often resulting in heterogeneous populations that contain undifferentiated cells. Here we developed a sensitive, target-specific, and general method for removing undesired cells before transplantation. MicroRNA-302a-5p (miR-302a) is highly and specifically expressed in human pluripotent stem cells and gradually decreases to basal levels during differentiation. We synthesized a new RNA tool, miR-switch, as a live-cell reporter mRNA for miR-302a activity that can specifically detect human induced pluripotent stem cells (hiPSCs) down to a spiked level of 0.05% of hiPSCs in a heterogeneous population and can prevent teratoma formation in an in vivo tumorigenicity assay. Automated and selective hiPSC-elimination was achieved by controlling puromycin resistance using the miR-302a switch. Our system uniquely provides sensitive detection of pluripotent stem cells and partially differentiated cells. In addition to its ability to eliminate undifferentiated cells, miR-302a switch also holds great potential in investigating the dynamics of differentiation and/or reprograming of live-cells based on intracellular information.

摘要

多能干细胞分化的效率高度可变,通常导致含有未分化细胞的异质群体。在这里,我们开发了一种在移植前去除不需要的细胞的敏感、靶向和通用方法。微 RNA-302a-5p(miR-302a)在人多能干细胞中高度特异性表达,并在分化过程中逐渐降低到基础水平。我们合成了一种新的 RNA 工具,miR-switch,作为 miR-302a 活性的活细胞报告 mRNA,可特异性检测异质群体中低至 0.05% 的人诱导多能干细胞(hiPSC),并可防止体内致瘤性试验中的畸胎瘤形成。通过使用 miR-302a 开关控制嘌呤霉素抗性,可以实现自动和选择性的 hiPSC 消除。我们的系统独特地提供了对多能干细胞和部分分化细胞的敏感检测。除了能够消除未分化细胞外,miR-302a 开关还具有在基于细胞内信息的活细胞分化和/或重编程中进行灵敏检测的巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b618/5016789/9391b50a3dde/srep32532-f5.jpg

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