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dc.contributor.authorGao, Shangbang
dc.contributor.authorXie, Lin
dc.contributor.authorKawano, Taizo
dc.contributor.authorPo, Michelle D.
dc.contributor.authorGuan, Sihui
dc.contributor.authorZhen, Mei
dc.contributor.authorPirri, Jennifer K.
dc.contributor.authorAlkema, Mark J
dc.date2022-08-11T08:09:29.000
dc.date.accessioned2022-08-23T16:32:35Z
dc.date.available2022-08-23T16:32:35Z
dc.date.issued2015-02-26
dc.date.submitted2016-11-04
dc.identifier.citationNat Commun. 2015 Feb 26;6:6323. doi: 10.1038/ncomms7323.
dc.identifier.issn2041-1723
dc.identifier.doi10.1038/ncomms7323
dc.identifier.pmid25716181
dc.identifier.urihttp://hdl.handle.net/20.500.14038/37915
dc.description<p>Co-author Jennifer Pirri is a doctoral student in the Neuroscience Program in the Graduate School of Biomedical Sciences (GSBS) at UMass Medical School.</p>
dc.description.abstractPersistent neural activity, a sustained circuit output that outlasts the stimuli, underlies short-term or working memory, as well as various mental representations. Molecular mechanisms that underlie persistent activity are not well understood. Combining in situ whole-cell patch clamping and quantitative locomotion analyses, we show here that the Caenorhabditis elegans neuromuscular system exhibits persistent rhythmic activity, and such an activity contributes to the sustainability of basal locomotion, and the maintenance of acceleration after stimulation. The NALCN family sodium leak channel regulates the resting membrane potential and excitability of invertebrate and vertebrate neurons. Our molecular genetics and electrophysiology analyses show that the C. elegans NALCN, NCA, activates a premotor interneuron network to potentiate persistent motor circuit activity and to sustain C. elegans locomotion. Collectively, these results reveal a mechanism for, and physiological function of, persistent neural activity using a simple animal model, providing potential mechanistic clues for working memory in other systems.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=25716181&dopt=Abstract">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1038/ncomms7323
dc.subjectNeural circuits
dc.subjectSodium channels
dc.subjectWorking memory
dc.subjectNeuroscience and Neurobiology
dc.titleThe NCA sodium leak channel is required for persistent motor circuit activity that sustains locomotion
dc.typeJournal Article
dc.source.journaltitleNature Communications
dc.source.volume6
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/neurobiology_pp/188
dc.identifier.contextkey9345739
html.description.abstract<p>Persistent neural activity, a sustained circuit output that outlasts the stimuli, underlies short-term or working memory, as well as various mental representations. Molecular mechanisms that underlie persistent activity are not well understood. Combining in situ whole-cell patch clamping and quantitative locomotion analyses, we show here that the Caenorhabditis elegans neuromuscular system exhibits persistent rhythmic activity, and such an activity contributes to the sustainability of basal locomotion, and the maintenance of acceleration after stimulation. The NALCN family sodium leak channel regulates the resting membrane potential and excitability of invertebrate and vertebrate neurons. Our molecular genetics and electrophysiology analyses show that the C. elegans NALCN, NCA, activates a premotor interneuron network to potentiate persistent motor circuit activity and to sustain C. elegans locomotion. Collectively, these results reveal a mechanism for, and physiological function of, persistent neural activity using a simple animal model, providing potential mechanistic clues for working memory in other systems.</p>
dc.identifier.submissionpathneurobiology_pp/188
dc.contributor.departmentGraduate School of Biomedical Sciences, Neuroscience Program
dc.contributor.departmentAlkema Lab
dc.contributor.departmentNeurobiology
dc.source.pages6323


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