2024
Translating Prefrontal Cortex Insights to the Clinic and Society
Rowe J, Datta D, Fiebach C, Jaeggi S, Liston C, Luna B, Rasmussen S, Roberts A, Sinha R, Haber S. Translating Prefrontal Cortex Insights to the Clinic and Society. 2024, 319-360. DOI: 10.7551/mitpress/15679.003.0019.Peer-Reviewed Original Research
2022
Outer hair cell function is normal in βV spectrin knockout mice
Stankewich MC, Bai JP, Stabach PR, Khan S, Tan WJT, Surguchev A, Song L, Morrow JS, Santos-Sacchi J, Navaratnam DS. Outer hair cell function is normal in βV spectrin knockout mice. Hearing Research 2022, 423: 108564. PMID: 35864018, DOI: 10.1016/j.heares.2022.108564.Peer-Reviewed Original ResearchConceptsOuter hair cellsAuditory brainstem response wavesAuditory thresholdOuter hair cell functionSpiral ganglion neuronsEfferent nerve fibersHair cell functionNumber of afferentsGanglion neuronsNerve fibersKnockout miceNeuronal structuresMiceHair cellsCell functionElectromechanical activityPutative roleType IOngoing investigationExon deletionsSynaptopathyAfferentsData supportResponse wavesNeurons
2019
Trio Haploinsufficiency Causes Neurodevelopmental Disease-Associated Deficits
Katrancha SM, Shaw JE, Zhao AY, Myers SA, Cocco AR, Jeng AT, Zhu M, Pittenger C, Greer CA, Carr SA, Xiao X, Koleske AJ. Trio Haploinsufficiency Causes Neurodevelopmental Disease-Associated Deficits. Cell Reports 2019, 26: 2805-2817.e9. PMID: 30840899, PMCID: PMC6436967, DOI: 10.1016/j.celrep.2019.02.022.Peer-Reviewed Original ResearchConceptsHeterozygous coding mutationsDendritic spine densityHippocampus of miceNeurodevelopmental disordersLong-term potentiationDendritic spine defectsPostsynaptic deficitsSpine densityCortical synapsesDendritic arborizationExcitatory neuronsMotor coordinationHaploinsufficient miceKnockout miceTherapeutic interventionsBipolar disorderProtein kinase A (PKA) signalingNeuronal structuresSpine defectsIncreases anxietyMiceDisordersDeficitsCoding mutationsA Signaling
2016
Differential expression of cytoskeletal regulatory factors in the adolescent prefrontal cortex: Implications for cortical development
Shapiro LP, Parsons RG, Koleske AJ, Gourley SL. Differential expression of cytoskeletal regulatory factors in the adolescent prefrontal cortex: Implications for cortical development. Journal Of Neuroscience Research 2016, 95: 1123-1143. PMID: 27735056, PMCID: PMC5352542, DOI: 10.1002/jnr.23960.Peer-Reviewed Original ResearchMeSH KeywordsAdolescentAge FactorsAnalysis of VarianceAnimalsBrain-Derived Neurotrophic FactorCytoskeletonDendritic SpinesFemaleGene Expression Regulation, DevelopmentalHumansIntegrin beta1MaleMembrane GlycoproteinsMiceMice, TransgenicNeural PathwaysNeuronsPrefrontal CortexReceptor, trkBSignal TransductionSynapsesSynaptophysinConceptsPrefrontal cortexDendritic spinesTropomyosin-related kinase receptor BDifferent adolescent agesKinase receptor BPrevalence of depressionMental health disordersDeep-layer excitatory neuronsRho kinase 2TrkB levelsVentral hippocampusOrbital prefrontal cortexAge-related differencesPsychiatric illnessReceptor BExcitatory neuronsPostnatal brainHealth disordersAnatomical connectionsNeuronal structuresWestern blottingAdolescent ageEarly adulthoodDramatic structural reorganizationPFC subregionsAn epigenetic mechanism mediates developmental nicotine effects on neuronal structure and behavior
Jung Y, Hsieh LS, Lee AM, Zhou Z, Coman D, Heath CJ, Hyder F, Mineur YS, Yuan Q, Goldman D, Bordey A, Picciotto MR. An epigenetic mechanism mediates developmental nicotine effects on neuronal structure and behavior. Nature Neuroscience 2016, 19: 905-914. PMID: 27239938, PMCID: PMC4925298, DOI: 10.1038/nn.4315.Peer-Reviewed Original Research
2014
Activity-Dependent Regulation of Dendritic Complexity by Semaphorin 3A through Farp1
Cheadle L, Biederer T. Activity-Dependent Regulation of Dendritic Complexity by Semaphorin 3A through Farp1. Journal Of Neuroscience 2014, 34: 7999-8009. PMID: 24899721, PMCID: PMC4044256, DOI: 10.1523/jneurosci.3950-13.2014.Peer-Reviewed Original ResearchConceptsDendritic complexityTotal dendritic branch lengthActivity-dependent regulationDendritic shaftsDendritic arborizationDendritic arborsHippocampal neuronsSynaptic inputsNeuronal activityRat neuronsSemaphorin 3ANeuronal structuresSema3ADendrite differentiationNeuronsRac1 activatorDendritic morphologyComplex neuronal structuresPlexinA1Soluble cuesSignaling proteinsArborizationFARP1CoreceptorChapter 5 ECM receptors in neuronal structure, synaptic plasticity, and behavior
Kerrisk ME, Cingolani LA, Koleske AJ. Chapter 5 ECM receptors in neuronal structure, synaptic plasticity, and behavior. Progress In Brain Research 2014, 214: 101-131. PMID: 25410355, PMCID: PMC4640673, DOI: 10.1016/b978-0-444-63486-3.00005-0.Peer-Reviewed Original ResearchConceptsSynaptic plasticityNeuronal structuresCentral nervous system developmentForm synapsesNervous system developmentDendritic projectionsSynaptic activityPostsynaptic partnersPostsynaptic cellECM receptorsReceptor activationGuidance moleculesSynapse structureReceptorsStable synapsesExtracellular matrix receptorsNeuronsSynapsesCell adhesion receptorsMatrix receptorsAdhesion receptorsReceptor transitionPreECM compositionECM ligands
2007
Long-term two-photon transcranial imaging of synaptic structures in the living brain.
Grutzendler J, Gan WB. Long-term two-photon transcranial imaging of synaptic structures in the living brain. Cold Spring Harbor Protocols 2007, 2007: pdb.prot4766. PMID: 21357119, DOI: 10.1101/pdb.prot4766.Peer-Reviewed Original ResearchLiving brainNeurological disease modelsMouse brain areasIndividual dendritic spinesAxonal varicositiesFrontal cortexDendritic spinesBrain areasTherapeutic interventionsSynaptic structureFunctional changesNeuronal structuresTranscranial imagingTwo-photon microscopyDisease modelsBrainLiving mouseSensitive toolImaging approachMemory processesImagingSomatosensoryVaricositiesCortexMice
2006
Two-photon imaging of synaptic plasticity and pathology in the living mouse brain
Grutzendler J, Gan WB. Two-photon imaging of synaptic plasticity and pathology in the living mouse brain. Neurotherapeutics 2006, 3: 489-496. PMID: 17012063, PMCID: PMC3593400, DOI: 10.1016/j.nurx.2006.07.005.Peer-Reviewed Original ResearchConceptsTwo-photon microscopyMouse brainAcute brain injuryPostsynaptic dendritic spinesAdult mouse brainCerebral ischemiaSynaptic pathologyCerebrovascular diseaseBrain injuryMouse modelDendritic spinesAnimal modelsBrain cellsIntact brainTwo-photon imagingNeuronal connectionsSynaptic plasticityAlzheimer's diseaseNeuronal structuresDiseaseBrainStructural plasticityPathologyTechnical considerationsIschemia
2001
Form and Function in Cells of the Brain
B.Levitan I, Kaczmarek L. Form and Function in Cells of the Brain. 2001, 25-44. DOI: 10.1093/oso/9780195145236.003.0002.Peer-Reviewed Original ResearchThe Birth and Death of a Neuron
B.Levitan I, Kaczmarek L. The Birth and Death of a Neuron. 2001, 375-394. DOI: 10.1093/oso/9780195145236.003.0015.Peer-Reviewed Original ResearchNervous systemNeuronal developmentProfound plastic changesAdult nerve cellsGrowth of axonsConnections of neuronsImmature neuronsSynaptic contactsNew neuronsNeuronal plasticityDendritic processesNeuronal formPlastic changesSynaptic connectionsNerve cellsNeuronal structuresNeuronsAdult animalsSelect groupDeathAdultsNormal courseCellsEarly stepsAxonsAdhesion Molecules and Axon Pathfinding
B.Levitan I, Kaczmarek L. Adhesion Molecules and Axon Pathfinding. 2001, 435-466. DOI: 10.1093/oso/9780195145236.003.0017.Peer-Reviewed Original ResearchNervous systemNeuronal activityDendritic branchesSuperior cervical ganglionDendritic branching patternsMature nervous systemTypes of synapsesIntact nervous systemCervical ganglionLong-term regulationSynaptic connectionsIntact animalsNeuronal structuresAdhesion moleculesNeuronsElectrical activityGangliaFluorescent cellsBranching patternDendritesCellsSpecific patternsAxonsMiceActivity
1998
Activation of Kv3.1 channels in neuronal spine-like structures may induce local potassium ion depletion
Wang L, Gan L, Perney T, Schwartz I, Kaczmarek L. Activation of Kv3.1 channels in neuronal spine-like structures may induce local potassium ion depletion. Proceedings Of The National Academy Of Sciences Of The United States Of America 1998, 95: 1882-1887. PMID: 9465111, PMCID: PMC19207, DOI: 10.1073/pnas.95.4.1882.Peer-Reviewed Original ResearchConceptsSpine-like structuresIon channelsMembrane structureMembrane compartmentsVesicle compartmentKv3.1 channelsBulk cytoplasmElectron immunomicroscopyCHO cellsPostsynaptic membraneVesiclesMembrane patchesSpine-like protrusionsNeuronal membrane structurePotassium channel Kv3.1Channel Kv3.1CellsComplete inactivationInactivationCompartmentsRapid depletionCentral nervous systemSlow refillingSynaptic stimulationNeuronal structures
1994
Oxygen deprivation activates an ATP-inhibitable K+ channel in substantia nigra neurons
Jiang C, Sigworth F, Haddad G. Oxygen deprivation activates an ATP-inhibitable K+ channel in substantia nigra neurons. Journal Of Neuroscience 1994, 14: 5590-5602. PMID: 8083755, PMCID: PMC6577106, DOI: 10.1523/jneurosci.14-09-05590.1994.Peer-Reviewed Original ResearchConceptsSubstantia nigra neuronsRat substantia nigra neuronsEffects of hypoxiaGlibenclamide binding sitesEffect of ATPCell-attached patchesNeuronal survivalKATP channelsResult of Ca2Different subtypesOutward currentsNeuronal structuresFree Ca2HypoxiaMetabolic stressNeuronsDeleterious changesSingle-channel currentsChannel activityO2 deprivationInternal ATPOxygen deprivationActivationHigh Ca2Membrane potential
1991
Ruthenium red inhibits tail skin vasodilatation evoked by intracerebroventricular injection of capsaicin in the rat
Hajós M, Janesó G, Mari Z, Obál F. Ruthenium red inhibits tail skin vasodilatation evoked by intracerebroventricular injection of capsaicin in the rat. Naunyn-Schmiedeberg's Archives Of Pharmacology 1991, 343: 431-433. PMID: 1712915, DOI: 10.1007/bf00179050.Peer-Reviewed Original ResearchConceptsCentral nervous systemIntracerebroventricular injectionNervous systemSkin vasodilatationRuthenium redCellular calcium metabolismCapsaicin-sensitive neuronsInjection of capsaicinPeripheral nervous systemTail skin temperatureTail skin vasodilatationCapsaicin-induced activationPeripheral vasodilatationCalcium metabolismMarked elevationAnesthetized ratsLateral ventricleRuthenium red inhibitsNerve cellsVasodilatationNeuronal structuresCapsaicinInjectionRatsNeurons
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