Impact of preconditioning with retinoic acid during early development on morphological and functional characteristics of human induced pluripotent stem cell-derived neurons

Human induced pluripotent stem cells (hiPSCs) are a suitable tool to study basic molecular and cellular mechanisms of neurodevelopment. The directed differentiation of hiPSCs via the generation of a self-renewable neuronal precursor cell line allows the standardization of defined differentiation pro...

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Hauptverfasser: Horschitz, Sandra (VerfasserIn) , Rosner, Jan (VerfasserIn) , Galach, Marta (VerfasserIn) , Greffrath, Wolfgang (VerfasserIn) , Treede, Rolf-Detlef (VerfasserIn) , Utikal, Jochen (VerfasserIn) , Schloss, Patrick (VerfasserIn) , Meyer-Lindenberg, Andreas (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: July 2015
In: Stem cell research
Year: 2015, Jahrgang: 15, Heft: 1, Pages: 30-41
ISSN:1876-7753
DOI:10.1016/j.scr.2015.04.007
Online-Zugang:Verlag, Volltext: http://dx.doi.org/10.1016/j.scr.2015.04.007
Verlag, Volltext: http://www.sciencedirect.com/science/article/pii/S1873506115000495
Volltext
Verfasserangaben:Sandra Horschitz, Friederike Matthäus, Anja Groß, Jan Rosner, Marta Galach, Wolfgang Greffrath, Rolf-Detlef Treede, Jochen Utikal, Patrick Schloss, Andreas Meyer-Lindenberg

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520 |a Human induced pluripotent stem cells (hiPSCs) are a suitable tool to study basic molecular and cellular mechanisms of neurodevelopment. The directed differentiation of hiPSCs via the generation of a self-renewable neuronal precursor cell line allows the standardization of defined differentiation protocols. Here, we have investigated whether preconditioning with retinoic acid during early neural induction impacts on morphological and functional characteristics of the neuronal culture after terminal differentiation. For this purpose we have analyzed neuronal and glial cell markers, neuronal outgrowth, soma size, depolarization-induced distal shifts of the axon initial segment as well as glutamate-evoked calcium influx. Retinoic acid preconditioning led to a higher yield of neurons vs. glia cells and longer axons than unconditioned controls. In contrast, glutamatergic activation and depolarization induced structural plasticity were unchanged. Our results show that the treatment of neuroectodermal cells with retinoic acid during early development, i.e. during the neurulation phase, increases the yield of neuronal phenotypes, but does not impact on the functionality of terminally differentiated neuronal cells. 
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