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NMDA receptor-dependent glutamate excitotoxicity in human embryonic stem cell-derived neurons.

TitleNMDA receptor-dependent glutamate excitotoxicity in human embryonic stem cell-derived neurons.
Publication TypeJournal Article
Year of Publication2013
AuthorsGupta K, Hardingham GE, Chandran S
JournalNeurosci Lett
Date Published2013 May 24
KeywordsCell Death, Cell Differentiation, Cells, Cultured, Dizocilpine Maleate, Embryonic Stem Cells, Glutamic Acid, Humans, Neurons, Protein Subunits, Receptors, AMPA, Receptors, N-Methyl-D-Aspartate, Time Factors

Thanks to the development of efficient differentiation strategies, human pluripotent stem cells (HPSC) offer the opportunity for modelling neuronal injury and dysfunction in human neurons in vitro. Critically, the effective use of HPSC-derived neural cells in disease-modelling and potentially cell replacement therapies hinges on an understanding of the biology of these cells, specifically their development, subtype specification and responses to neurotoxic signalling mediators. Here, we generated neurons from human embryonic stem cells and characterised the development of vulnerability to glutamate excitotoxicity, a key contributor to neuronal injury in several acute and chronic neurodegenerative disorders. Over two months of differentiation we observed a gradual increase in responsiveness of neurons to glutamate-induced Ca(2+) influx, attributable to NMDA receptor activity. This increase was concomitant with an increase in expression of mRNA encoding NMDA and AMPA receptor subunits. Differentiated neurons were vulnerable to glutamate excitotoxicity in a dose-dependent manner, which was reduced by NMDA receptor antagonists.

Alternate JournalNeurosci. Lett.
PubMed ID23518152
PubMed Central IDPMC3725411
Grant ListG0902044 / / Medical Research Council / United Kingdom
/ / Biotechnology and Biological Sciences Research Council / United Kingdom
/ / Medical Research Council / United Kingdom
/ / Wellcome Trust / United Kingdom
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