grant

Structure and function of spontaneous network activity during circuit formation

Organization DUKE UNIVERSITYLocation DURHAM, UNITED STATESPosted 15 Dec 2020Deadline 31 Mar 2027
NIHUS FederalResearch GrantFY2026ASDAddressAffectAnatomic SitesAnatomic structuresAnatomyAssayAutismAutistic DisorderBehaviorBehavioralBioassayBiologic ModelsBiological AssayBiological ModelsCalciumCalcium BindingCandidate Disease GeneCandidate GeneCell BodyCellsCognitionConnector NeuronDataDefectDevelopmentDrosophilaDrosophila genusEarly Infantile AutismElectron MicroscopeEmbryoEmbryonicEmotionsEpilepsyEpileptic SeizuresEpilepticsFoundationsFutureGenesGeneticGoalsHumanImageIndividualInfantile AutismIntercalary NeuronIntercalated NeuronsInterneuronsInternuncial CellInternuncial NeuronKanner's SyndromeKnowledgeLabelLearningLinkLocomotionMapsMembraneMethodsModel SystemModelingModern ManMolecularMolecular FingerprintingMolecular ProfilingMonitorMotorMotor outputMusculoskeletal SystemNerve CellsNerve UnitNervous SystemNeural CellNeural DevelopmentNeural TransmissionNeurocyteNeurodevelopmental DisorderNeurologic Body SystemNeurologic Organ SystemNeurological Development DisorderNeuronsNeurosciencesOrganismOrthologOrthologous GenePatternPerceptionPhasePopulationProcessPropertyRNA interference screenRNAi screenRNAi-based screenRapid screeningResearchSeizure DisorderSensoryStereotypingStimulusStochastic ProcessesStructureSynaptic TransmissionSystemTechniquesTestingTimeTrainingTransmissionWorkautism spectral disorderautism spectrum disorderautistic spectrum disordercalcium boundcell typeconnectomedevelopmentalepilepsiaepileptogenicfruit flyhatchingimaginginsightintervention designknock-downknockdownlarva controllarval controlliving systemlocomotor systemmembrane structuremolecular profilemolecular signaturenervous system developmentneuralneural circuitneural circuitryneural mechanismneurocircuitryneurodevelopmentneurodevelopmental diseaseneuromechanismneuronalnoveloptogeneticspost-doctoral trainingprogramsquantitative imagingspatial and temporalspatial temporalspatiotemporalstereotypystochastic methodsynaptic circuitsynaptic circuitrytherapy designtooltransmission processtreatment design
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Full Description

Project Summary
Towards the end of nervous system development, neural circuits are extremely plastic. Small perturbations

during this time can cause lifelong circuit and behavioral changes. Not surprisingly, mounting evidence suggests

that several neurodevelopmental disorders, including autism spectrum disorder and epilepsy, have origins in

defective late neural circuit formation. During this late stage, neural circuits refinement takes place, and

components of the mature behavior gradually appear. As this occurs, stimulus-independent bursts of activity

sweep through neuronal populations. This type of activity, known as spontaneous network activity (SNA), has

been characterized in vertebrate systems where it refines neural connections to generate sensory maps and

establish local circuits. However, we know surprisingly little about the molecular mechanisms by which SNA is

initiated, how it functions, and how it ultimately underpins behavior. This proposal establishes the developing

Drosophila larval locomotor system as a genetically tractable model, with a wealth of knowledge on early stages

of neurodevelopment and circuit function, where these questions can be tackled. We combine genetic and

systems neuroscience techniques to gain new understanding into SNA function during late circuit formation. This

proposal has three goals. (1) The exact neurons that initiate SNA within locomotor circuits are not known. The

first aim of this proposal is to identify the SNA initiator neurons and the mechanism by which they act. Uncovering

the mechanism that initiates SNA at the neural and activity level is fundamental to understand how SNA is

implemented. (2) After initiation, SNA expands and begins to produce motor outputs that mature into the larval

behavior. How does this activity pattern develop? The second aim of this proposal is to reveal the structure of

SNA at the population level and the pattern of activity in individual neurons, and begin to learn the effect of SNA

on mature behavior. (3) The molecular mechanisms that produce SNA remain poorly understood in any

organism. The third aim will identify genes that are necessary for the initiation and/or expansion of SNA. We will

focus on genes that have been associated with neurodevelopmental disorders, which intriguingly are highly

expressed specifically during the SNA window. In sum, this proposal will reveal the neural mechanisms for how

SNA initiates, the structure and neural components of SNA after initiation, and genes required for SNA. These

studies will provide new insight into how neural circuits form, or fail to form properly, in neurodevelopmental

disorders.

Grant Number: 5R00NS119295-05
NIH Institute/Center: NIH

Principal Investigator: Arnaldo Carreira-Rosario

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