Novel surface-enhanced Raman scattering-based assays for ultra-sensitive detection of human pluripotent stem cells

被引:27
|
作者
Han, Jingjia [1 ,2 ]
Qian, Ximei [3 ,4 ]
Wu, Qingling [1 ,2 ,3 ,4 ]
Jha, Rajneesh [1 ,2 ]
Duan, Jinshuai [6 ]
Yang, Zhou [6 ]
Maher, Kevin O. [1 ,2 ]
Nie, Shuming [3 ,4 ,5 ]
Xu, Chunhui [1 ,2 ,3 ,4 ]
机构
[1] Emory Univ, Sch Med, Dept Pediat, Div Pediat Cardiol, Atlanta, GA 30322 USA
[2] Childrens Healthcare Atlanta, Atlanta, GA 30322 USA
[3] Emory Univ, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30322 USA
[4] Georgia Inst Technol, Atlanta, GA 30322 USA
[5] Nanjing Univ, Coll Engn & Appl Sci, Nanjing 210093, Jiangsu, Peoples R China
[6] Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Human pluripotent stem cell; Differentiation; Flow cytometry; Nanoparticle; SERS assay; TERATOMA FORMATION; BIOMEDICAL APPLICATIONS; NANOPARTICLES; CARDIOMYOCYTES; ELIMINATION; SERS; DIFFERENTIATION; TUMORIGENICITY; INHIBITION; MATURATION;
D O I
10.1016/j.biomaterials.2016.07.033
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Human pluripotent stem cells (hPSCs) are a promising cell source for regenerative medicine, but their derivatives need to be rigorously evaluated for residual stem cells to prevent teratoma formation. Here, we report the development of novel surface-enhanced Raman scattering (SERS)-based assays that can detect trace numbers of undifferentiated hPSCs in mixed cell populations in a highly specific, ultra sensitive, and time-efficient manner. By targeting stem cell surface markers SSEA-5 and TRA-1-60 individually or simultaneously, these SERS assays were able to identify as few as I stem cell in 106 cells, a sensitivity (0.0001%) which was 2000 to 15,000-fold higher than that of flow cytometry assays. Using the SERS assay, we demonstrate that the aggregation of hPSC-based cardiomyocyte differentiation cultures into 3D spheres significantly reduced SSEA-5+ and TRA-1-60+ cells compared with parallel 2D cultures. Thus, SERS may provide a powerful new technology for quality control of hPSC-derived products for preclinical and clinical applications. (C) 2016 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.orgilicenses/by-nc-nd/4.0/).
引用
收藏
页码:66 / 76
页数:11
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