Synaptic to circuit homeostasis in the Drosophila locomotor system
Synaptic to circuit homeostasis in the Drosophila locomotor system
批准号:
10654556
负责人:
Ehud Isacoff
金额:
$30.87万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-07-01 至 2024-06-30
关键词:
3-DimensionalAction PotentialsAddressAxonBehaviorBehavioralBrainCellsCompensationDiseaseDrosophila genusElectrophysiology (science)EnsureEquilibriumEvoked PotentialsExcitatory SynapseFrequenciesGeneticGlutamatesGoalsHealthHeterogeneityHomeostasisImageMapsMethodsMolecularMotor NeuronsMuscleMusculoskeletal SystemNervous SystemNeuromuscular JunctionNeuronsNoiseOpticsOutputPatternPreparationProbabilityProcessPropertyProteinsRNA InterferenceSignal TransductionSiteSynapsesSynaptic TransmissionSynaptic plasticitySystemWeightWorkcell typegenetic regulatory proteinimaging systemin vivoinformation processinginsightknock-downneuralneural circuitneuromechanismneurotransmitter releasenovelpostsynapticpreservationpresynapticprotein expressionrecruitsuperresolution imagingtranscriptometransmission processultra high resolution
中文摘要
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英文摘要
What sets the transmission strength of synapses? What determines their plasticity properties? How do
synapses homeostatically adjust synaptic weight to accommodate to changing conditions and ensure robust
behavior? What happens if synaptic homeostasis is insufficient to compensate for a disruption or a change in
demand, are other backup mechnisms of compensation recruited and, if so, how do they work? We combine in
vivo super-resolution quantal imaging of synaptic transmission and behavioral analysis with focused RNAi
knockdown in one cell type and single cell transcriptome analysis to address these questions. Our preparation
is the Drosophila larval neuromuscular junction—an ideal system for imaging and genetics, which shares
synaptic signaling machinery and functional properties with vertebrate central excitatory synapses. Our in vivo
quantal analysis has revealed that two converging glutamatergic motor neuron (MN) inputs have great
heterogeneity in evoked release probability (Pr) and short-term plasticity and that only Ib undergoes “synaptic
homeostasis,” whereby transmitter release changes to compensate for altered postsynaptic sensitivity. Our
goal is to identify the molecules responsible for the synapse to synapse and input to input differences. Equally
exciting, preliminary work suggests the existence of a novel layer of gain control: “circuit homeostasis,” which
is recruited when synaptic transmission is so compromised that “synaptic homeostasis” cannot compensate
sufficiently. The circuit homeostasis system adjusts neural firing pattern in the presynaptic cell and upstream
circuit to preserve locomotor behavior when synaptic transmission is inadequate. Our goal is to define the
mechanisms that assure neural output by setting and adjusting transmitter release and firing dynamics.
Progress will provide fundamental insight into the robustness of the nervous system that preserves health and
which may cause disease when it goes awry.
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