Dissecting Neural Circuit Computations in the Peripheral Visual System
Dissecting Neural Circuit Computations in the Peripheral Visual System
批准号:
10183257
负责人:
Thomas Robert Clandinin
金额:
$38.07万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-08-01 至 2023-05-31
关键词:
AlgorithmsAnimalsArchitectureArithmeticBehaviorBehavioralBlindnessBrainCellsComplexCuesDataDendritesDevelopmentDiseaseDissectionDrosophila genusElementsGABA ReceptorGeneticGoalsHealthHumanIndividualIon ChannelIon Channel GatingLightLinkMathematicsModelingMolecularMotionMovementNeuronsNeurosciencesNoiseOutputPatternPerceptionPeripheralPhotoreceptorsProcessPropertyRetinaRoleSignal TransductionStimulusStructureSynapsesSystemTechniquesTestingVisionVisualVisual CortexVisual system structurecell behaviorcell typedeprivationdetectorexperienceflygenetic manipulationin vivo calcium imagingneural circuitoperationoptogeneticsorientation selectivitypostsynapticreceptive fieldrelating to nervous systemresponseretinal prosthesissensory inputtheoriesvirtualvisual informationvisual processingvisual stimulusvoltage
中文摘要
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英文摘要
Project Summary
R01 EY022638
Dissecting neural circuit computations in the peripheral visual system
PI: Thomas R. Clandinin
Vision provides critical sensory inputs that guide our routine behaviors; as a result, blindness
represents perhaps the most devastating deprivation we can experience. To connect perception to action in
this context, complex visual scenes must be efficiently represented in the neural activities of relatively small
groups of cells; from these signals, particularly salient cues are extracted, integrated with behavioral goals, and
linked to the appropriate responses. These neural processes can be broken down into the individual actions of
relatively simple microcircuits, small groups of neurons that perform elementary operations that are widespread
in the brain, but which subserve distinct purposes in different contexts. This proposal develops the Drosophila
visual system as a model in which the functions of these microcircuits can be dissected at the molecular,
cellular and behavioral level, and combines techniques drawn from genetics and systems neuroscience to
derive new understanding.
This proposal focuses on three computations that are central to vision. First, one fundamental circuit
process in the visual system transforms the intensity of a light signal into an estimate of contrast, the change in
light level relative to a previous intensity. This transformation corresponds to taking the mathematical derivative
of an input, an operation that is performed in many circuits, but one whose circuit and molecular
implementation is unknown. The first goal of this proposal is to determine how this operation is implemented at
the circuit and molecular level. Second, the ability to detect motion is probably the most critical visual signal
extracted by the brain, providing information central to guiding movement and navigation. The emergence of
this direction-selectivity in the brain represents a long-standing, paradigmatic neural computation with rich
theoretical underpinnings. However, the circuit and molecular implementations of these theories are only
incompletely understood. The second goal of this proposal is to identify and dissect the microcircuits that first
extract motion signals. Third, the tuning of visual neurons for oriented edges is central to representing the
spatial structure of the world. Again, the mechanisms that allow neurons to become tuned for these features
are only incompletely understood. The third goal of this proposal is to determine the structure and functional
architecture of orientation selective circuitry.
These studies will broadly inform our understanding of retinal function in health and disease. As the
development of retinal prostheses that directly stimulate specific circuit elements represents an important
treatment possibility for blindness, understanding how these circuits can encode behaviorally-relevant visual
information represents a important goal.
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Neurons Rho to Get in Shape for the Day.
神经元 Rho 为一天保持体形。
DOI:
10.1016/j.cell.2015.07.044
发表时间:
2015
期刊:
Cell
影响因子:
64.5
作者:
[Mann,Kevin, Clandinin,ThomasR]
通讯作者:
Clandinin,ThomasR
DOI:
10.1038/nn.3600
发表时间:
2014-02
期刊:
NATURE NEUROSCIENCE
影响因子:
25
作者:
[Clark, Damon A., Fitzgerald, James E., Ales, Justin M., Gohl, Daryl M., Silies, Marion A., Norcia, Anthony M., Clandinin, Thomas R.]
通讯作者:
Clandinin, Thomas R.
Linear Summation Underlies Direction Selectivity in Drosophila.
线性求和是果蝇方向选择性的基础。
DOI:
10.1016/j.neuron.2018.07.005
发表时间:
2018
期刊:
Neuron
影响因子:
16.2
作者:
[Wienecke,CarlFR, Leong,JonathanCS, Clandinin,ThomasR]
通讯作者:
Clandinin,ThomasR
DOI:
10.1016/j.neuron.2013.04.024
发表时间:
2013-06-19
期刊:
Neuron
影响因子:
16.2
作者:
[Freifeld L, Clark DA, Schnitzer MJ, Horowitz MA, Clandinin TR]
通讯作者:
Clandinin TR
DOI:
10.7554/elife.25690
发表时间:
2017-07-27
期刊:
ELIFE
影响因子:
7.7
作者:
[Chamberland, Simon, Yang, Helen H., St-Pierre, Francois]
通讯作者:
St-Pierre, Francois
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海外基金