Comparison of spike parameters from optically identified GABAergic and glutamatergic neurons in sparse cortical cultures
Primary neuronal cultures share many typical features with the in vivo situation, including similarities in distinct electrical activity patterns and synaptic network interactions. Here, we use multi-electrode array (MEA) recordings from spontaneously active cultures of wildtype and GAD67-GFP transg...
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doaj-bf2f5da6c84a479ca286394d29c39b042020-11-24T23:42:40ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022015-01-01810.3389/fncel.2014.00460120711Comparison of spike parameters from optically identified GABAergic and glutamatergic neurons in sparse cortical culturesHeiko J Luhmann0Keiko eWeir1Oriane eBlanquie2Werner eKilb3Anne eSinning4Institut für PhysiologieInstitut für PhysiologieInstitut für PhysiologieInstitut für PhysiologieInstitut für PhysiologiePrimary neuronal cultures share many typical features with the in vivo situation, including similarities in distinct electrical activity patterns and synaptic network interactions. Here, we use multi-electrode array (MEA) recordings from spontaneously active cultures of wildtype and GAD67-GFP transgenic mice to evaluate which spike parameters differ between GABAergic interneurons and principal, putatively glutamatergic neurons. To analyze this question we combine MEA recordings with optical imaging in sparse cortical cultures to assign individual spikes to visually-identified single neurons. In our culture system, excitatory and inhibitory neurons are present at a similar ratio as described in vivo, and spike waveform characteristics and firing patterns are fully developed after two weeks in vitro. Spike amplitude, but not other spike waveform parameters, correlated with the distance between the recording electrode and the location of the assigned neuron´s soma. Cluster analysis of spike waveform properties revealed no particular cell population that may be assigned to putative inhibitory or excitatory neurons. Moreover, experiments in primary cultures from transgenic GAD67-GFP mice, which allow optical identification of GABAergic interneurons and thus unambiguous assignment of extracellular signals, did not reveal any significant difference in spike timing and spike waveform parameters between inhibitory and excitatory neurons. Despite of our detailed characterization of spike waveform and temporal spiking properties we could not identify an unequivocal electrical parameter to discriminate between individual excitatory and inhibitory neurons in vitro. Our data suggest that under in vitro conditions cellular classifications of single neurons on the basis of their extracellular firing properties should be treated with caution.http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00460/fullInterneuronsimagingMulti-Electrode Arraynetwork activityneuronal culturespike waveform |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Heiko J Luhmann Keiko eWeir Oriane eBlanquie Werner eKilb Anne eSinning |
spellingShingle |
Heiko J Luhmann Keiko eWeir Oriane eBlanquie Werner eKilb Anne eSinning Comparison of spike parameters from optically identified GABAergic and glutamatergic neurons in sparse cortical cultures Frontiers in Cellular Neuroscience Interneurons imaging Multi-Electrode Array network activity neuronal culture spike waveform |
author_facet |
Heiko J Luhmann Keiko eWeir Oriane eBlanquie Werner eKilb Anne eSinning |
author_sort |
Heiko J Luhmann |
title |
Comparison of spike parameters from optically identified GABAergic and glutamatergic neurons in sparse cortical cultures |
title_short |
Comparison of spike parameters from optically identified GABAergic and glutamatergic neurons in sparse cortical cultures |
title_full |
Comparison of spike parameters from optically identified GABAergic and glutamatergic neurons in sparse cortical cultures |
title_fullStr |
Comparison of spike parameters from optically identified GABAergic and glutamatergic neurons in sparse cortical cultures |
title_full_unstemmed |
Comparison of spike parameters from optically identified GABAergic and glutamatergic neurons in sparse cortical cultures |
title_sort |
comparison of spike parameters from optically identified gabaergic and glutamatergic neurons in sparse cortical cultures |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Cellular Neuroscience |
issn |
1662-5102 |
publishDate |
2015-01-01 |
description |
Primary neuronal cultures share many typical features with the in vivo situation, including similarities in distinct electrical activity patterns and synaptic network interactions. Here, we use multi-electrode array (MEA) recordings from spontaneously active cultures of wildtype and GAD67-GFP transgenic mice to evaluate which spike parameters differ between GABAergic interneurons and principal, putatively glutamatergic neurons. To analyze this question we combine MEA recordings with optical imaging in sparse cortical cultures to assign individual spikes to visually-identified single neurons. In our culture system, excitatory and inhibitory neurons are present at a similar ratio as described in vivo, and spike waveform characteristics and firing patterns are fully developed after two weeks in vitro. Spike amplitude, but not other spike waveform parameters, correlated with the distance between the recording electrode and the location of the assigned neuron´s soma. Cluster analysis of spike waveform properties revealed no particular cell population that may be assigned to putative inhibitory or excitatory neurons. Moreover, experiments in primary cultures from transgenic GAD67-GFP mice, which allow optical identification of GABAergic interneurons and thus unambiguous assignment of extracellular signals, did not reveal any significant difference in spike timing and spike waveform parameters between inhibitory and excitatory neurons. Despite of our detailed characterization of spike waveform and temporal spiking properties we could not identify an unequivocal electrical parameter to discriminate between individual excitatory and inhibitory neurons in vitro. Our data suggest that under in vitro conditions cellular classifications of single neurons on the basis of their extracellular firing properties should be treated with caution. |
topic |
Interneurons imaging Multi-Electrode Array network activity neuronal culture spike waveform |
url |
http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00460/full |
work_keys_str_mv |
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