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Antipsychotics promote neural differentiation of human iPS cell-derived neural stem cells.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2016 Nov 25; Vol. 480 (4), pp. 615-621. Date of Electronic Publication: 2016 Oct 26. - Publication Year :
- 2016
-
Abstract
- We investigated the effects of antipsychotics on human induced pluripotent stem cell (hiPSC)-derived neural stem cell (NSC) differentiation. Induction of NSCs from hiPSCs was performed using PSC neural induction medium. Induced NSCs were subsequently cultured in neural differentiation medium containing antipsychotics. Cultured cells were subjected to neural differentiation marker analysis. As previously shown in rodent cells, antipsychotics promoted neural differentiation compared with vehicle treatment. Atypical antipsychotics appear to possess more differentiation induction potential than typical ones. Most NSCs do not express dopamine D2 receptor; however, our in vitro study indicates the clinical potential of antipsychotics could include effects independent of monoamine receptor expression in NSCs. Our study shows NSCs derived from hiPSCs provide opportunity to investigate the underlying direct effect of antipsychotics treatment on NSCs.<br /> (Copyright © 2016 Elsevier Inc. All rights reserved.)
- Subjects :
- Cell Differentiation physiology
Cells, Cultured
Dose-Response Relationship, Drug
Humans
Induced Pluripotent Stem Cells physiology
Neural Stem Cells physiology
Neurogenesis physiology
Neurogenesis radiation effects
Receptors, Dopamine D1 metabolism
Antipsychotic Agents pharmacology
Cell Differentiation drug effects
Induced Pluripotent Stem Cells cytology
Induced Pluripotent Stem Cells drug effects
Neural Stem Cells cytology
Neural Stem Cells drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 480
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 27793669
- Full Text :
- https://doi.org/10.1016/j.bbrc.2016.10.102