| Literature DB >> 27647668 |
Sheng Dai1,2, Rong Li1, Yan Long1,3, Steve Titus1, Jinghua Zhao1, Ruili Huang1, Menghang Xia1, Wei Zheng1.
Abstract
Human neuronal cells differentiated from induced pluripotent cells have emerged as a new model system for the study of disease pathophysiology and evaluation of drug efficacy. Differentiated neuronal cells are more similar in genetics and biological content to human brain cells than other animal disease models. However, culture of neuronal cells in assay plates requires a labor-intensive procedure of plate precoating, hampering its applications in high-throughput screening (HTS). We developed a simplified method with one-step seeding of neural stem cells in assay plates by supplementing the medium with a recombinant human vitronectin (VTN), thus avoiding plate precoating. Robust results were obtained from cell viability, calcium response, and neurite outgrowth assays using this new method. Our data demonstrate that this approach greatly simplifies high-throughput assays using neuronal cells differentiated from human stem cells for translational research.Entities:
Keywords: HTS; high-content screening; high-throughput screening; iPSC; induced pluripotent stem cells; neural stem cells; neuronal cells; plate coating; vitronectin
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Year: 2016 PMID: 27647668 PMCID: PMC5285267 DOI: 10.1177/1087057116670068
Source DB: PubMed Journal: J Biomol Screen ISSN: 1087-0571