Promoting optic nerve and retinofugal pathway regeneration
Promoting optic nerve and retinofugal pathway regeneration
批准号:
9338034
负责人:
Andrew D Huberman
金额:
$39.38万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-12-01 至 2019-11-30
关键词:
AddressAdultAlzheimer&aposs DiseaseAnimalsAxonAxotomyBackBlindnessBrainCell NucleusClinicalCollectionDataDiseaseEyeFRAP1 geneGeneticGlaucomaGoalsGrowthHealthHome environmentHumanIn VitroInjuryKnowledgeLabelLeadMolecularMusNatural regenerationNerve CrushNeuronsOptic NerveOutputPathway interactionsPatternPhotic StimulationPlayPropertyRecovery of FunctionResearchResolutionRetinalRetinal DegenerationRetinal Ganglion CellsRoleSignal TransductionSpecificitySpinal CordStimulusStructureSynapsesSystemTestingVisionVisualVisual PathwaysVisual system structureaxon growthaxon regenerationbehavior measurementcell growthcell typeexperienceexperimental studyin vivo regenerationinjuredmTOR inhibitionnoveloptic nerve disorderprogramsreconstructionrepairedresponseresponse to injuryrestorationselective expressiontool
中文摘要
项目摘要/摘要
这个研究项目的总体目标是了解如何再生
哺乳动物的中枢视觉通路。这项建议特别关注这个问题。
如何从眼睛的输出神经元,视网膜神经节细胞再生投射
(视网膜节细胞)到它们在大脑中的靶点(统称为‘视黄醇逃逸途径’)-a
巡回赛绝对是必不可少的视觉。最近在以下方面取得了重大进展
识别能够触发RGC轴突再生的分子程序。这个
该领域的下一个关键里程碑是找到增加RGC数量的方法
再生的轴突及其再生的距离。同样至关重要的是,
确定重新生成的RGC是否可以找到并重新连接到正确的目标,
这样的视觉能力又回来了。这项提议的三个主要目的是:1)测试
假设特定形式的视觉刺激可以增加数量和
RGC再生轴突的距离2)检验结合视觉的假说
分子刺激RGC轴突生长可导致RGC轴突再生
长距离回到大脑中,并决定再生的视网膜节细胞是否
能够返回并重新连接到适当的目标,以及
避开不符合其功能的目标。这些实验的结果应该会导致
对哺乳动物视觉回路如何进行反应的新理解
以伤害和铺平道路的培养适用于人类遭受
视力丧失。
英文摘要
Project Summary/Abstract
The overall goal of this research program is to understand how to regenerate
mammalian central visual pathways. This proposal specifically focuses on the question
of how to regenerate projections from output neurons of the eye, retinal ganglion cells
(RGCs) to their targets in the brain (collectively referred to `retinofugal pathway')- a
circuit absolutely essential vision. Significant progress has recently been made in
identifying molecular programs capable of triggering some RGC axon regeneration. The
next crucial milestones for the field are to discover ways to increase the number RGC
axons that regenerate and the distance they regro. It is also crucially important to
determine whether regenerating RGCs can find and reconnect to the correct targets,
such visual capacities return. The three major aims of this proposal are to: 1) test the
hypothesis that specific forms of visual stimulation can enhance the number and
distance of RGC regenerating axons 2) test the hypothesis that combining visual
stimulation with molecular triggers of RGC axon growth can cause RGC axons to regrow
long distances back into the brain and 3) determine whether regenerating RGCs are
capable of pathfinding back to and re-connecting to their appropriate targets, as well as
avoiding targets incorrect for their function. Results from these experiments should lead
to new understanding of how mammalian visual circuits can be replenished in response
to injury and pave the way for the cultivation of tools applicable to humans suffering from
vision loss.
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会议论文
Development of retinofugal parallel pathways
-
批准号:8222232
-
项目类别:
-
资助金额:$37.97万
-
财政年份:2012
-
负责人:Andrew D Huberman
-
依托单位:
Development of retinofugal parallel pathways
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批准号:8609572
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项目类别:
-
资助金额:$36.97万
-
财政年份:2012
-
负责人:Andrew D Huberman
-
依托单位:
Development of retinofugal parallel pathways
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批准号:9338070
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项目类别:
-
资助金额:$8.71万
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财政年份:2012
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负责人:Andrew D Huberman
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依托单位:
Development of retinofugal parallel pathways
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批准号:8795719
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项目类别:
-
资助金额:$36.87万
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财政年份:2012
-
负责人:Andrew D Huberman
-
依托单位:
Development of retinofugal parallel pathways
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批准号:8411123
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项目类别:
-
资助金额:$35.92万
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财政年份:2012
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负责人:Andrew D Huberman
-
依托单位:
Development of retinofugal parallel pathways
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批准号:9003053
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项目类别:
-
资助金额:$28.79万
-
财政年份:2012
-
负责人:Andrew D Huberman
-
依托单位:
Neurogenetics of Vision
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批准号:9373699
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项目类别:
-
资助金额:$15.04万
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财政年份:--
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负责人:Andrew D Huberman
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依托单位:
Neurogenetics of Vision
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批准号:10006571
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项目类别:
-
资助金额:$15.04万
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财政年份:--
-
负责人:Andrew D Huberman
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依托单位:
海外基金