Veterinärmedizinische Universität Wien Forschungsinformationssystem VetDoc

Grafischer Link zur Startseite der Vetmeduni Vienna

Gewählte Publikation:

Publikationstyp: Zeitschriftenaufsatz
Dokumenttyp: Originalarbeit

Jahr: 2012

AutorInnen: Visan, A; Hayess, K; Sittner, D; Pohl, EE; Riebeling, C; Slawik, B; Gulich, K; Oelgeschläger, M; Luch, A; Seiler, AE

Titel: Neural differentiation of mouse embryonic stem cells as a tool to assess developmental neurotoxicity in vitro.

Quelle: Neurotoxicology. 2012; 33(5):1135-1146

Autor/innen der Vetmeduni Vienna:

Pohl Elena

Beteiligte Vetmed-Organisationseinheiten
Institut für Physiologie, Pathophysiologie und Biophysik, Abteilung für Physiologie und Biophysik

Mouse embryonic stem cells (mESCs) represent an attractive cellular system for in vitro studies in developmental biology as well as toxicology because of their potential to differentiate into all fetal cell lineages. The present study aims to establish an in vitro system for developmental neurotoxicity testing employing mESCs. We developed a robust and reproducible protocol for fast and efficient differentiation of the mESC line D3 into neural cells, optimized with regard to chemical testing. Morphological examination and immunocytochemical staining confirmed the presence of different neural cell types, including neural progenitors, neurons, astrocytes, oligodendrocytes, and radial glial cells. Neurons derived from D3 cells expressed the synaptic proteins PSD95 and synaptophysin, and the neurotransmitters serotonin and γ-aminobutyric acid. Calcium ion imaging revealed the presence of functionally active glutamate and dopamine receptors. In addition, flow cytometry analysis of the neuron-specific marker protein MAP2 on day 12 after induction of differentiation demonstrated a concentration dependent effect of the neurodevelopmental toxicants methylmercury chloride, chlorpyrifos, and lead acetate on neuronal differentiation. The current study shows that D3 mESCs differentiate efficiently into neural cells involving a neurosphere-like state and that this system is suitable to detect adverse effects of neurodevelopmental toxicants. Therefore, we propose that the protocol for differentiation of mESCs into neural cells described here could constitute one component of an in vitro testing strategy for developmental neurotoxicity.

Keywords Pubmed: 2",3"-Cyclic-Nucleotide Phosphodiesterases/metabolism
Astrocytes/drug effects
Cell Differentiation/drug effects
Cell Differentiation/physiology*
Cell Line
Cell Proliferation
Cell Survival
Embryonic Stem Cells/drug effects
Embryonic Stem Cells/physiology*
Flow Cytometry
Glial Fibrillary Acidic Protein/metabolism
Guanylate Kinase/metabolism
Membrane Proteins/metabolism
Methylmercury Compounds/toxicity
Microtubule-Associated Proteins/metabolism
Neurons/drug effects
Oligodendroglia/drug effects
Organometallic Compounds/toxicity
Sodium Glutamate/toxicity
Time Factors
Tyrosine 3-Monooxygenase/metabolism
alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid/pharmacology

© Veterinärmedizinische Universität Wien Hilfe und DownloadsErklärung zur Barrierefreiheit