Please use this identifier to cite or link to this item: https://doi.org/10.3389/fnmol.2018.00261
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dc.titlePatch-Seq Protocol to Analyze the Electrophysiology, Morphology and Transcriptome of Whole Single Neurons Derived From Human Pluripotent Stem Cells
dc.contributor.authorvan den Hurk, M.
dc.contributor.authorErwin, J.A.
dc.contributor.authorYeo, G.W.
dc.contributor.authorGage, F.H.
dc.contributor.authorBardy, C.
dc.date.accessioned2021-12-09T05:01:03Z
dc.date.available2021-12-09T05:01:03Z
dc.date.issued2018
dc.identifier.citationvan den Hurk, M., Erwin, J.A., Yeo, G.W., Gage, F.H., Bardy, C. (2018). Patch-Seq Protocol to Analyze the Electrophysiology, Morphology and Transcriptome of Whole Single Neurons Derived From Human Pluripotent Stem Cells. Frontiers in Molecular Neuroscience 11 : 261. ScholarBank@NUS Repository. https://doi.org/10.3389/fnmol.2018.00261
dc.identifier.issn1662-5099
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/210094
dc.description.abstractThe human brain is composed of a complex assembly of about 171 billion heterogeneous cellular units (86 billion neurons and 85 billion non-neuronal glia cells). A comprehensive description of brain cells is necessary to understand the nervous system in health and disease. Recently, advances in genomics have permitted the accurate analysis of the full transcriptome of single cells (scRNA-seq). We have built upon such technical progress to combine scRNA-seq with patch-clamping electrophysiological recording and morphological analysis of single human neurons in vitro. This new powerful method, referred to as Patch-seq, enables a thorough, multimodal profiling of neurons and permits us to expose the links between functional properties, morphology, and gene expression. Here, we present a detailed Patch-seq protocol for isolating single neurons from in vitro neuronal cultures. We have validated the Patch-seq whole-transcriptome profiling method with human neurons generated from embryonic and induced pluripotent stem cells (ESCs/iPSCs) derived from healthy subjects, but the procedure may be applied to any kind of cell type in vitro. Patch-seq may be used on neurons in vitro to profile cell types and states in depth to unravel the human molecular basis of neuronal diversity and investigate the cellular mechanisms underlying brain disorders. © 2018 van den Hurk, Erwin, Yeo, Gage and Bardy.
dc.publisherFrontiers Media S.A.
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2018
dc.subjectCellular phenotyping
dc.subjectElectrophysiology
dc.subjectHuman neuron transcriptome
dc.subjectInduced pluripotent stem cell (iPSC)
dc.subjectNeuronal diversity
dc.subjectPatch clamping
dc.subjectPatch-seq
dc.subjectSingle-cell RNA-seq
dc.typeArticle
dc.contributor.departmentDEPT OF PHYSIOLOGY
dc.description.doi10.3389/fnmol.2018.00261
dc.description.sourcetitleFrontiers in Molecular Neuroscience
dc.description.volume11
dc.description.page261
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