| Literature DB >> 30519939 |
Masin Abo-Rady1, Jessica Bellmann1, Michael Glatza2, Lara Marrone1, Lydia Reinhardt1,2, Santiago Tena1, Jared Sterneckert3.
Abstract
High-throughput phenotypic screening enables the identification of new therapeutic targets even when the molecular mechanism underlying the disease is unknown. In the case of neurodegenerative disease, there is a dire need to identify new targets that can ameliorate, halt, or reverse degeneration. Stem cell-based disease models are particularly powerful tools for phenotypic screening because they use the same cell type affected in patients. Here, we describe the expansion of mouse stem cells and human induced pluripotent stem cells as well as the differentiation of these cells into neural lineages that, when exposed to neuroinflammatory stress, can be used for compound screening followed by hit identification, validation, and target deconvolution.Entities:
Keywords: Disease modelling; Neurodegeneration; Neuroinflammation; Neuronal differentiation; Phenotypic screening; Pluripotent stem cells; Target deconvolution
Mesh:
Substances:
Year: 2019 PMID: 30519939 DOI: 10.1007/978-1-4939-8891-4_2
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745