A high-throughput model for investigating neuronal function and synaptic transmission in cultured neuronal networks
Autor: | Jasmeet K Virdee, Joanna Wolak, Filipa M. Ferreira, Daniel Ursu, Gabriella Saro, Antoine Fouillet, Jeremy Findlay, Sarah Eversden, Michael J. O'Neill |
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Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Cations Divalent Phenotypic screening Primary Cell Culture lcsh:Medicine AMPA receptor Biology Neurotransmission Synaptic Transmission Article Rats Sprague-Dawley 03 medical and health sciences 0302 clinical medicine Drug Discovery Biological neural network Animals lcsh:Science Cells Cultured Cultured neuronal network Cerebral Cortex Neurons Neurotransmitter Agents Multidisciplinary Drug discovery lcsh:R Electric Stimulation Voltage-Sensitive Dye Imaging 030104 developmental biology Synapses NMDA receptor Calcium lcsh:Q Metabotropic glutamate receptor 2 Neuroscience 030217 neurology & neurosurgery |
Zdroj: | Scientific Reports, Vol 7, Iss 1, Pp 1-14 (2017) Scientific Reports |
ISSN: | 2045-2322 |
DOI: | 10.1038/s41598-017-15171-5 |
Popis: | Loss of synapses or alteration of synaptic activity is associated with cognitive impairment observed in a number of psychiatric and neurological disorders, such as schizophrenia and Alzheimer’s disease. Therefore successful development of in vitro methods that can investigate synaptic function in a high-throughput format could be highly impactful for neuroscience drug discovery. We present here the development, characterisation and validation of a novel high-throughput in vitro model for assessing neuronal function and synaptic transmission in primary rodent neurons. The novelty of our approach resides in the combination of the electrical field stimulation (EFS) with data acquisition in spatially separated areas of an interconnected neuronal network. We integrated our methodology with state of the art drug discovery instrumentation (FLIPR Tetra) and used selective tool compounds to perform a systematic pharmacological validation of the model. We investigated pharmacological modulators targeting pre- and post-synaptic receptors (AMPA, NMDA, GABA-A, mGluR2/3 receptors and Nav, Cav voltage-gated ion channels) and demonstrated the ability of our model to discriminate and measure synaptic transmission in cultured neuronal networks. Application of the model described here as an unbiased phenotypic screening approach will help with our long term goals of discovering novel therapeutic strategies for treating neurological disorders. |
Databáze: | OpenAIRE |
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