Development of Visual Pathways
Development of Visual Pathways
批准号:
8519455
负责人:
HWAI-JONG CHENG
金额:
$27.22万
依托单位国家:
美国
项目类别:
财政年份:
1996
资助国家:
美国
项目状态:
已结题
起止时间:
1996-07-01 至 2015-07-31
关键词:
Action PotentialsAddressAdultAffectAmacrine CellsAnimalsAntibodiesAttention deficit hyperactivity disorderAutistic DisorderAxonBasic ScienceBelief SystemBlindnessBrainBrain InjuriesCell physiologyCellsClinicalContralateralDataDevelopmentDiffuseDiseaseDoseEpilepsyEyeEye DevelopmentFamilyFerretsFetal Alcohol SyndromeFire - disastersFutureGoalsHumanImageryImaging TechniquesImmunotoxinsInjection of therapeutic agentIpsilateralLabelLaboratoriesLateral Geniculate BodyLeadLearningLifeLightMemoryMethodsNervous system structureNeurodevelopmental DisorderNeuronsOcular dominance columnsPathway interactionsPatternPlayPotassium ChannelProblem SolvingProteinsRecoveryRetinalRetinal Ganglion CellsRibosomesRoleSchizophreniaShapesSimulateSocietiesSpecificityStagingStrokeStructureStudy modelsSynapsesTargeted ToxinsTechniquesTestingTimeToxinTracerTraumaUncertaintyVisionVisual PathwaysVisual system structureVitreous humorWorkacetylcholine transporterarea striatabasecell killingdesigndevelopmental neurobiologyexperiencemodel developmentmonocular deprivationpostnatalpreventpublic health relevancereceptive fieldrepairedresearch studyretinogeniculatesegregationsensorimotor systemsensory system
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): In the mature mammalian visual system, information from the two eyes is anatomically segregated into layers in the lateral geniculate nucleus, and into ocular dominance columns in primary visual cortex. During the past half century, the development of this segregation has served as a premier model for the development of specific connections in the brain. Groundbreaking work in the 1960s showed that neuronal activity is important for the normal development of ocular dominance columns. If poor vision or no vision is experienced by one eye early in life, then that eye loses anatomical and functional connections to the brain. This results in blindness through the affected eye later in life, even if the cause of the poor vision is fixed so that the eye itself functions normally. Many studies over the ensuing years have looked at the effects of altering or abolishing neuronal activity on the development of eye-specific segregation. Findings from these studies lead to the following conclusions: 1) During development, specific connections in the visual system emerge over time from initially diffuse connections, 2) abolishing retinal activity during development maintains the initial imprecise connections, and 3) temporal correlation in the firing patterns of neurons within each eye, and lack of correlation between eyes is responsible for the development of eye-specific connections. These conclusions formed the dogma of the field of development of sensory systems, and significantly influenced related fields such as neurodevelopmental disorders, adult plasticity in the brain, and learning and memory. However, new experiments over the past decade have questioned each of these conclusions. This proposal will address the controversies by performing the following specific aims. 1) What is the normal pattern of development of ocular dominance columns? Anatomical tracing methods will be used to determine whether afferents serving the two eyes are initially overlapping or segregated in primary visual cortex. 2) What is the effect of complete retinal activity blockade on the development of eye-specific segregation in the LGN and cortex? Pharmacological agents will be used to silence retinal ganglion cell action potentials during development, and the effects on segregation will be examined. 3) What aspects of retinal ganglion cell activity are important for normal development of eye-specificity in the LGN? Manipulations that alter patterns of activity in the retina will be compared in order to determine which aspects of activity patterns are associated with normal segregation versus lack of segregation. 4) What is the role of correlated activity in the development of segregation? Light activatable molecules will be used to control activity patterns to determine whether increased correlation of firing of neighboring cells between the two eyes leads to lack of eye-specific segregation. These experiments will not only help to resolve important basic science controversies, but will also have clinical implications. Understanding the initial state of connections in the brain, the effects of absent or altered activity, and the key aspects of activity patterns that are needed for normal development, will all aid in the understanding and eventual treatment of neurodevelopmental disorders.
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DOI:
10.1002/ar.21001
发表时间:
2010-01
期刊:
ANATOMICAL RECORD-ADVANCES IN INTEGRATIVE ANATOMY AND EVOLUTIONARY BIOLOGY
影响因子:
2
作者:
[Speer, Colenso M., Mikula, Shawn, Huberman, Andrew D., Chapman, Barbara]
通讯作者:
Chapman, Barbara
No ON-OFF maps in supragranular layers of ferret visual cortex.
雪貂视觉皮层的颗粒上层没有开关图。
DOI:
10.1152/jn.2002.88.4.2163
发表时间:
2002
期刊:
Journal of neurophysiology
影响因子:
2.5
作者:
[Chapman,Barbara, Gödecke,Imke]
通讯作者:
Gödecke,Imke
Cortical cell orientation selectivity fails to develop in the absence of ON-center retinal ganglion cell activity.
如果中心视网膜神经节细胞没有活动,皮质细胞方向选择性就无法发展。
DOI:
10.1523/jneurosci.20-05-01922.2000
发表时间:
2000
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
[Chapman,B, Gödecke,I]
通讯作者:
Gödecke,I
Grading the thalamus: how can an 'Eph' be excellent?
丘脑分级:“Eph”如何才能优秀?
DOI:
10.1017/s1472928807000234
发表时间:
2005
期刊:
Thalamus & related systems
影响因子:
--
作者:
[Speer,ColensoM, Chapman,Barbara]
通讯作者:
Chapman,Barbara
Mouse mutants for the nicotinic acetylcholine receptor ß2 subunit display changes in cell adhesion and neurodegeneration response genes.
烟碱乙酰胆碱受体 2 亚基的小鼠突变体表现出细胞粘附和神经退行性反应基因的变化。
DOI:
10.1371/journal.pone.0018626
发表时间:
2011
期刊:
PloS one
影响因子:
3.7
作者:
[Rubin,CarolM, vanderList,DeborahA, Ballesteros,JoseM, Goloshchapov,AndreyV, Chalupa,LeoM, Chapman,Barbara]
通讯作者:
Chapman,Barbara
Neuronal Integration of Newborn Granule Cells in Aged Brains
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批准号:9381932
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项目类别:
-
资助金额:$31.28万
-
财政年份:2017
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负责人:HWAI-JONG CHENG
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依托单位:
Development of a non-rodent model using light-activated channel technology to cur
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批准号:8045374
-
项目类别:
-
资助金额:$18.41万
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财政年份:2010
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负责人:HWAI-JONG CHENG
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依托单位:
PLEXINS AND MOLECULAR MECHANISMS OF AXON GUIDANCE
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批准号:7929855
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项目类别:
-
资助金额:$10.41万
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财政年份:2009
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负责人:HWAI-JONG CHENG
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依托单位:
PLEXINS AND MOLECULAR MECHANISMS OF AXON GUIDANCE
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批准号:7069636
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项目类别:
-
资助金额:$26.12万
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财政年份:2004
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负责人:HWAI-JONG CHENG
-
依托单位:
PLEXINS AND MOLECULAR MECHANISMS OF AXON GUIDANCE
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批准号:6823798
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项目类别:
-
资助金额:$26.24万
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财政年份:2004
-
负责人:HWAI-JONG CHENG
-
依托单位:
PLEXINS AND MOLECULAR MECHANISMS OF AXON GUIDANCE
-
批准号:6942322
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项目类别:
-
资助金额:$26.75万
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财政年份:2004
-
负责人:HWAI-JONG CHENG
-
依托单位:
PLEXINS AND MOLECULAR MECHANISMS OF AXON GUIDANCE
-
批准号:7455788
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项目类别:
-
资助金额:$24.93万
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财政年份:2004
-
负责人:HWAI-JONG CHENG
-
依托单位:
PLEXINS AND MOLECULAR MECHANISMS OF AXON GUIDANCE
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批准号:7232105
-
项目类别:
-
资助金额:$25.44万
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财政年份:2004
-
负责人:HWAI-JONG CHENG
-
依托单位:
Development of Visual Pathways
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批准号:8311769
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项目类别:
-
资助金额:$28.66万
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财政年份:1996
-
负责人:HWAI-JONG CHENG
-
依托单位:
海外基金