Critical Period Plasticity and Binocular Matching in the Visual Cortex
视觉皮层的关键期可塑性和双眼匹配
基本信息
- 批准号:10356026
- 负责人:
- 金额:$ 39.16万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2010
- 资助国家:美国
- 起止时间:2010-09-30 至 2024-02-29
- 项目状态:已结题
- 来源:
- 关键词:AdultAgeAmblyopiaBinocular VisionBiological ModelsBirthBrainCalciumCellsChronicClinicalCognitiveCortical BlindnessDarknessDataDevelopmentDiseaseDorsalElectrophysiology (science)Exposure toEyeGoalsGrantHumanImageIndividualInterneuronsKnowledgeLabelLateral Geniculate BodyLifeLinkMental disordersModelingMotorMusNervous System PhysiologyNervous system structureNeurodevelopmental DisorderNeuronsNeurophysiology - biologic functionOcular DominanceOutcomeParvalbuminsPathway interactionsPhysiologicalPlayProcessPropertyRecoveryReportingResearchResearch PersonnelRoleSensorySeriesShapesSiliconSiteSomatostatinStrabismusSynapsesThalamic structureTimeTransfectionTransgenic MiceV1 neuronViralVisualVisual CortexVisual system structureWhole-Cell Recordingsarea striataautism spectrum disordercritical developmental periodcritical perioddensitydevelopmental plasticityexperienceexperimental studyin vivoinhibitory neuronmonocularmonocular deprivationmouse modelnervous system disorderneural circuitneurodevelopmentnovelorientation selectivityreceptive fieldresponsesocialtwo-photonvisual deprivationvisual processing
项目摘要
Project Summary/Abstract
Optimal functioning of the nervous system requires selective wiring of neural circuits, the precision of
which is achieved through experience-dependent refinement after birth. A classic model system of experience-
dependent neural development is ocular dominance plasticity in the visual system, where monocular visual
deprivation in a critical period of early life alters cortical responses. The investigators have recently discovered
that normal binocular vision in the critical period drives the matching of orientation preference between the two
eyes in the visual cortex, thus revealing a physiological purpose for critical period plasticity in normal
development. The proposed experiments aim to study cortical and thalamic mechanisms that underlie the
binocular matching process. In aim one, two-photon calcium imaging will be performed chronically to reveal how
individual cortical cells change their monocular orientation tunings to match between the two eyes. In addition,
two-photon imaging and electrophysiological recording will be used to characterize the binocular response
properties of subtypes of inhibitory neurons before, during, and after the critical period. In aim two,
electrophysiological recordings will be conducted to determine whether there are more binocular neurons in the
dorsal lateral geniculate nucleus (dLGN) of young mice than in adults, and whether these binocular dLGN
neurons show significant matching in their orientation preference before V1. Additional experiments will be
performed to determine whether the early matching in the dLGN is experience-dependent by recording from
mice reared in complete darkness from birth. Finally, by combining cortical silencing and in vivo whole cell
recording, the investigators will examine whether the binocular responses of dLGN input determine the binocular
tuning of individual V1 neurons. Together, these experiments will reveal a novel link between the developmental
plasticity at two successive stages of visual processing, and determine the role of visual thalamus in guiding
binocular development in V1. Because ocular dominance plasticity and its critical period is a model for amblyopia
and strabismus, a full understanding of cortical and subcortical changes that normally take place during
development will have profound implications for the understanding and treatment of these diseases.
项目总结/摘要
神经系统的最佳功能需要神经回路的选择性布线,
这是通过出生后的经验依赖的改进来实现的。一个经典的经验模型系统-
依赖性神经发育是视觉系统中的眼优势可塑性,其中单眼视觉
在生命早期的关键时期,剥夺会改变大脑皮层的反应。调查人员最近发现
关键期正常的双眼视觉驱动着两者之间的方位偏好匹配
眼睛在视觉皮层,从而揭示了生理目的的关键期可塑性,在正常
发展拟议的实验旨在研究大脑皮层和丘脑的机制,
双目匹配过程在第一个目标中,双光子钙成像将长期进行,以揭示如何
单个皮层细胞改变它们的单眼定向调谐以在两只眼睛之间匹配。此外,本发明还提供了一种方法,
双光子成像和电生理记录将用于表征双眼反应
在关键期之前、期间和之后,抑制性神经元亚型的特性。在目标二,
将进行电生理记录以确定大脑中是否有更多的双眼神经元
背外侧膝状体核(dLGN)的年轻小鼠比成年小鼠,以及是否这些双眼dLGN
神经元在V1前表现出明显的方向偏好匹配。其他实验将
执行以确定dLGN中的早期匹配是否是经验依赖性的,
老鼠从出生起就在完全黑暗的环境中长大。最后,通过结合皮质沉默和体内全细胞,
记录,研究人员将检查dLGN输入的双眼反应是否决定双眼
单个V1神经元的调谐。总之,这些实验将揭示一个新的联系之间的发展
可塑性的两个连续阶段的视觉处理,并确定视觉丘脑的作用,指导
V1期双眼发育。由于眼优势可塑性及其关键期是弱视的模型
和斜视,充分了解皮质和皮质下的变化,通常发生在
发展将对理解和治疗这些疾病产生深远影响。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Jianhua Cang其他文献
Jianhua Cang的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Jianhua Cang', 18)}}的其他基金
Visual Signal Transformation in the Retinocollicular Pathway
视网膜小球通路中的视觉信号转换
- 批准号:
9187019 - 财政年份:2015
- 资助金额:
$ 39.16万 - 项目类别:
Critical Period Plasticity and Binocular Matching in the Visual Cortex
视觉皮层的关键期可塑性和双眼匹配
- 批准号:
9885133 - 财政年份:2010
- 资助金额:
$ 39.16万 - 项目类别:
Critical Period Plasticity and Binocular Matching in the Visual Cortex
视觉皮层的关键期可塑性和双眼匹配
- 批准号:
8509700 - 财政年份:2010
- 资助金额:
$ 39.16万 - 项目类别:
Critical Period Plasticity and Binocular Matching in the Visual Cortex
视觉皮层的关键期可塑性和双眼匹配
- 批准号:
8144766 - 财政年份:2010
- 资助金额:
$ 39.16万 - 项目类别:
Critical Period Plasticity and Binocular Matching in the Visual Cortex
视觉皮层的关键期可塑性和双眼匹配
- 批准号:
7948969 - 财政年份:2010
- 资助金额:
$ 39.16万 - 项目类别:
Critical Period Plasticity and Binocular Matching in the Visual Cortex
视觉皮层的关键期可塑性和双眼匹配
- 批准号:
10591534 - 财政年份:2010
- 资助金额:
$ 39.16万 - 项目类别:
相似国自然基金
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
- 批准号:JCZRQN202500010
- 批准年份:2025
- 资助金额:0.0 万元
- 项目类别:省市级项目
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
- 批准号:2025JJ70209
- 批准年份:2025
- 资助金额:0.0 万元
- 项目类别:省市级项目
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
- 批准号:
- 批准年份:2024
- 资助金额:0 万元
- 项目类别:面上项目
甜茶抑制AGE-RAGE通路增强突触可塑性改善小鼠抑郁样行为
- 批准号:2023JJ50274
- 批准年份:2023
- 资助金额:0.0 万元
- 项目类别:省市级项目
蒙药额尔敦-乌日勒基础方调控AGE-RAGE信号通路改善术后认知功能障碍研究
- 批准号:
- 批准年份:2022
- 资助金额:33 万元
- 项目类别:地区科学基金项目
补肾健脾祛瘀方调控AGE/RAGE信号通路在再生障碍性贫血骨髓间充质干细胞功能受损的作用与机制研究
- 批准号:
- 批准年份:2022
- 资助金额:52 万元
- 项目类别:面上项目
LncRNA GAS5在2型糖尿病动脉粥样硬化中对AGE-RAGE 信号通路上相关基因的调控作用及机制研究
- 批准号:
- 批准年份:2022
- 资助金额:10.0 万元
- 项目类别:省市级项目
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
- 批准号:81973577
- 批准年份:2019
- 资助金额:55.0 万元
- 项目类别:面上项目
AGE/RAGE通路microRNA编码基因多态性与2型糖尿病并发冠心病的关联研究
- 批准号:81602908
- 批准年份:2016
- 资助金额:18.0 万元
- 项目类别:青年科学基金项目
高血糖激活滑膜AGE-RAGE-PKC轴致骨关节炎易感的机制研究
- 批准号:81501928
- 批准年份:2015
- 资助金额:18.0 万元
- 项目类别:青年科学基金项目
相似海外基金
Collaborative Research: Resolving the LGM ventilation age conundrum: New radiocarbon records from high sedimentation rate sites in the deep western Pacific
合作研究:解决LGM通风年龄难题:西太平洋深部高沉降率地点的新放射性碳记录
- 批准号:
2341426 - 财政年份:2024
- 资助金额:
$ 39.16万 - 项目类别:
Continuing Grant
Collaborative Research: Resolving the LGM ventilation age conundrum: New radiocarbon records from high sedimentation rate sites in the deep western Pacific
合作研究:解决LGM通风年龄难题:西太平洋深部高沉降率地点的新放射性碳记录
- 批准号:
2341424 - 财政年份:2024
- 资助金额:
$ 39.16万 - 项目类别:
Continuing Grant
PROTEMO: Emotional Dynamics Of Protective Policies In An Age Of Insecurity
PROTEMO:不安全时代保护政策的情绪动态
- 批准号:
10108433 - 财政年份:2024
- 资助金额:
$ 39.16万 - 项目类别:
EU-Funded
The role of dietary and blood proteins in the prevention and development of major age-related diseases
膳食和血液蛋白在预防和发展主要与年龄相关的疾病中的作用
- 批准号:
MR/X032809/1 - 财政年份:2024
- 资助金额:
$ 39.16万 - 项目类别:
Fellowship
Atomic Anxiety in the New Nuclear Age: How Can Arms Control and Disarmament Reduce the Risk of Nuclear War?
新核时代的原子焦虑:军控与裁军如何降低核战争风险?
- 批准号:
MR/X034690/1 - 财政年份:2024
- 资助金额:
$ 39.16万 - 项目类别:
Fellowship
Walkability and health-related quality of life in Age-Friendly Cities (AFCs) across Japan and the Asia-Pacific
日本和亚太地区老年友好城市 (AFC) 的步行适宜性和与健康相关的生活质量
- 批准号:
24K13490 - 财政年份:2024
- 资助金额:
$ 39.16万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Discovering the (R)Evolution of EurAsian Steppe Metallurgy: Social and environmental impact of the Bronze Age steppes metal-driven economy
发现欧亚草原冶金的(R)演变:青铜时代草原金属驱动型经济的社会和环境影响
- 批准号:
EP/Z00022X/1 - 财政年份:2024
- 资助金额:
$ 39.16万 - 项目类别:
Research Grant
ICF: Neutrophils and cellular senescence: A vicious circle promoting age-related disease.
ICF:中性粒细胞和细胞衰老:促进与年龄相关疾病的恶性循环。
- 批准号:
MR/Y003365/1 - 财政年份:2024
- 资助金额:
$ 39.16万 - 项目类别:
Research Grant
Doctoral Dissertation Research: Effects of age of acquisition in emerging sign languages
博士论文研究:新兴手语习得年龄的影响
- 批准号:
2335955 - 财政年份:2024
- 资助金额:
$ 39.16万 - 项目类别:
Standard Grant
Shaping Competition in the Digital Age (SCiDA) - Principles, tools and institutions of digital regulation in the UK, Germany and the EU
塑造数字时代的竞争 (SCiDA) - 英国、德国和欧盟的数字监管原则、工具和机构
- 批准号:
AH/Y007549/1 - 财政年份:2024
- 资助金额:
$ 39.16万 - 项目类别:
Research Grant














{{item.name}}会员




