Phenotypic Screening Using Mouse and Human Stem Cell-Based Models of Neuroinflammation and Gene Expression Analysis to Study Drug Responses.
Animals
Astrocytes
/ cytology
Cell Culture Techniques
Cell Differentiation
Drug Discovery
/ methods
Drug Evaluation, Preclinical
/ methods
High-Throughput Screening Assays
Humans
Mice
Neural Stem Cells
/ cytology
Neurons
/ cytology
Phenotype
Reproducibility of Results
Small Molecule Libraries
Stem Cells
/ cytology
Disease modelling
Neurodegeneration
Neuroinflammation
Neuronal differentiation
Phenotypic screening
Pluripotent stem cells
Target deconvolution
Journal
Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969
Informations de publication
Date de publication:
2019
2019
Historique:
entrez:
7
12
2018
pubmed:
7
12
2018
medline:
5
6
2019
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 30519939
doi: 10.1007/978-1-4939-8891-4_2
doi:
Substances chimiques
Small Molecule Libraries
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM