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dc.contributor.authorPitman, Jena L.
dc.contributor.authorHuetteroth, Wolf
dc.contributor.authorBurke, Christopher J.
dc.contributor.authorKrashes, Michael Jonathan
dc.contributor.authorLai, Sen-Lin
dc.contributor.authorLee, Tzumin
dc.contributor.authorWaddell, Scott
dc.date2022-08-11T08:08:54.000
dc.date.accessioned2022-08-23T16:11:35Z
dc.date.available2022-08-23T16:11:35Z
dc.date.issued2011-05-24
dc.date.submitted2011-05-23
dc.identifier.citationCurr Biol. 2011 May 24;21(10):855-861. <a href="http://dx.doi.org/10.1016/j.cub.2011.03.069">Link to article on publisher's site</a>
dc.identifier.issn0960-9822 (Linking)
dc.identifier.doi10.1016/j.cub.2011.03.069
dc.identifier.pmid21530258
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33204
dc.description.abstractLabile memory is thought to be held in the brain as persistent neural network activity [1-4]. However, it is not known how biologically relevant memory circuits are organized and operate. Labile and persistent appetitive memory in Drosophila requires output after training from the alpha'beta' subset of mushroom body (MB) neurons and from a pair of modulatory dorsal paired medial (DPM) neurons [5-9]. DPM neurons innervate the entire MB lobe region and appear to be pre- and postsynaptic to the MB [7, 8], consistent with a recurrent network model. Here we identify a role after training for synaptic output from the GABAergic anterior paired lateral (APL) neurons [10, 11]. Blocking synaptic output from APL neurons after training disrupts labile memory but does not affect long-term memory. APL neurons contact DPM neurons most densely in the alpha'beta' lobes, although their processes are intertwined and contact throughout all of the lobes. Furthermore, APL contacts MB neurons in the alpha' lobe but makes little direct contact with those in the distal alpha lobe. We propose that APL neurons provide widespread inhibition to stabilize and maintain synaptic specificity of a labile memory trace in a recurrent DPM and MB alpha'beta' neuron circuit.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=21530258&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.cub.2011.03.069
dc.subjectDrosophila; Appetite; Neurons; Memory; Olfactory Perception; Drosophila Proteins
dc.subjectNeuroscience and Neurobiology
dc.titleA Pair of Inhibitory Neurons Are Required to Sustain Labile Memory in the Drosophila Mushroom Body
dc.typeJournal Article
dc.source.journaltitleCurrent biology : CB
dc.source.volume21
dc.source.issue10
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/1742
dc.identifier.contextkey2025445
html.description.abstract<p>Labile memory is thought to be held in the brain as persistent neural network activity [1-4]. However, it is not known how biologically relevant memory circuits are organized and operate. Labile and persistent appetitive memory in Drosophila requires output after training from the alpha'beta' subset of mushroom body (MB) neurons and from a pair of modulatory dorsal paired medial (DPM) neurons [5-9]. DPM neurons innervate the entire MB lobe region and appear to be pre- and postsynaptic to the MB [7, 8], consistent with a recurrent network model. Here we identify a role after training for synaptic output from the GABAergic anterior paired lateral (APL) neurons [10, 11]. Blocking synaptic output from APL neurons after training disrupts labile memory but does not affect long-term memory. APL neurons contact DPM neurons most densely in the alpha'beta' lobes, although their processes are intertwined and contact throughout all of the lobes. Furthermore, APL contacts MB neurons in the alpha' lobe but makes little direct contact with those in the distal alpha lobe. We propose that APL neurons provide widespread inhibition to stabilize and maintain synaptic specificity of a labile memory trace in a recurrent DPM and MB alpha'beta' neuron circuit.</p>
dc.identifier.submissionpathgsbs_sp/1742
dc.contributor.departmentMorningside Graduate School of Biomedical Sciences
dc.contributor.departmentWaddell Lab
dc.contributor.departmentLee Lab
dc.contributor.departmentNeurobiology
dc.source.pages855-861
dc.contributor.studentChristopher Burke
dc.contributor.studentMichael Krashes
dc.contributor.studentSen-Lin Lai
dc.description.thesisprogramNeuroscience


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