| Literature DB >> 27509304 |
Jingjia Han1, Ximei Qian2, Qingling Wu3, Rajneesh Jha1, Jinshuai Duan4, Zhou Yang4, Kevin O Maher1, Shuming Nie5, Chunhui Xu6.
Abstract
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 1 stem cell in 10(6) 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.Entities:
Keywords: Differentiation; Flow cytometry; Human pluripotent stem cell; Nanoparticle; SERS assay
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Year: 2016 PMID: 27509304 PMCID: PMC5391677 DOI: 10.1016/j.biomaterials.2016.07.033
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479