Wile Brian M, Ban Kiwon, Yoon Young-Sup, Bao Gang
1] Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia, USA. [2].
1] Division of Cardiology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, USA. [2].
Nat Protoc. 2014 Oct;9(10):2411-24. doi: 10.1038/nprot.2014.154. Epub 2014 Sep 18.
Molecular beacons (MBs) are dual-labeled oligonucleotides that fluoresce only in the presence of complementary mRNA. The use of MBs to target specific mRNAs allows sorting of specific cells from a mixed cell population. In contrast to existing approaches that are limited by available surface markers or selectable metabolic characteristics, the MB-based method enables the isolation of a wide variety of cells. For example, the ability to purify specific cell types derived from pluripotent stem cells (PSCs) is important for basic research and therapeutics. In addition to providing a general protocol for MB design, validation and nucleofection into cells, we describe how to isolate a specific cell population from differentiating PSCs. By using this protocol, we have successfully isolated cardiomyocytes differentiated from mouse or human PSCs (hPSCs) with ∼ 97% purity, as confirmed by electrophysiology and immunocytochemistry. After designing MBs, their ordering and validation requires 2 weeks, and the isolation process requires 3 h.
分子信标(MBs)是一种双标记寡核苷酸,仅在存在互补mRNA时才会发出荧光。利用MBs靶向特定mRNA能够从混合细胞群体中筛选出特定细胞。与受可用表面标志物或可选择代谢特征限制的现有方法不同,基于MBs的方法能够分离多种细胞。例如,从多能干细胞(PSC)中纯化特定细胞类型的能力对于基础研究和治疗学而言至关重要。除了提供MB设计、验证及导入细胞的核转染通用方案外,我们还描述了如何从分化的PSC中分离特定细胞群体。通过使用该方案,我们已成功分离出从小鼠或人PSC(hPSC)分化而来的心肌细胞,经电生理学和免疫细胞化学证实,其纯度约为97%。设计MBs后,订购和验证需要2周时间,分离过程需要3小时。