SYNAPTIC TRANSMISSION AND ITS MODULATION IN THE RETINA
视网膜中的突触传递及其调节
基本信息
- 批准号:7994760
- 负责人:
- 金额:$ 39.47万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1991
- 资助国家:美国
- 起止时间:1991-05-01 至 2012-11-30
- 项目状态:已结题
- 来源:
- 关键词:Amacrine CellsBrainCellsConflict (Psychology)GoalsLateralLight AdaptationsMediatingOutputPathway interactionsPhotoreceptorsPrincipal InvestigatorProcessRelative (related person)RetinaRetinalRetinal Ganglion CellsRoleShapesSignal PathwaySignal TransductionStreamSynaptic TransmissionVisualVisual system structurecell typeganglion cellhorizontal cellneural circuitouter plexiform layerprogramsreceptive fieldresponse
项目摘要
DESCRIPTION (provided by applicant): Spatial and contrast information are first processed by the visual system within the retina. The processing of these aspects of the visual scene depends on the center-surround, receptive field organization of retinal ganglion cells. While it is known that activation of the concentric regions of the receptive field produces opponent responses in ganglion cells, the retinal circuitry responsible for this receptive field organization remains poorly understood. The center signal is carried by the input-output pathway consisting of photoreceptors, bipolar cells and ganglion cells. However, the lateral pathways that mediate surround signals remain unclear. Conflicting evidence suggests that either horizontal cells in the outer retina or amacrine cells in the inner retina mediate surround signaling. The relative roles of these pathways in ganglion cell receptive field formation are poorly understood. Different features of the visual world are extracted by 10-15 different ganglion cell types, which are then sent to the brain in distinct processing streams. The receptive field organization of these distinct ganglion cells may be uniquely shaped by different inner and outer retinal surround contributions. Ganglion cell receptive fields can also be altered by light adaptation, but it is not known how the inner and outer retina contributes to these changes. The goal of this proposal is to determine the circuitry and synaptic mechanisms responsible for the receptive field variety found across ganglion cells. Electrophysiological, pharmacological and anatomical approaches will be used to determine how inner and outer retinal surround pathways shape the receptive fields in morphologically distinct ganglion cells. Three specific aims will determine 1) the roles of the outer retina in GC receptive field organization 2) determine the roles of the inner retina in GC receptive field organization and 3) determine how light adaptation modifies the inner and outer retinal contributions to GC receptive field organization. By defining the precise roles of inner and outer plexiform layers that mediate surround signaling in specific GC types, we will develop a more complete picture of how spatial and contrast information is processed by distinct visual signaling pathways.
描述(由申请人提供):空间和对比度信息首先由视网膜内的视觉系统处理。视觉场景的这些方面的处理取决于视网膜神经节细胞的中心-环绕、感受野组织。虽然已知感受野的同心区域的激活在神经节细胞中产生对抗反应,但负责该感受野组织的视网膜回路仍然知之甚少。中心信号通过由光感受器、双极细胞和神经节细胞组成的输入-输出通路传递。然而,介导周围信号的侧向通路仍不清楚。现有证据表明,外视网膜中的水平细胞或内视网膜中的无长突细胞介导环绕信号。这些通路在神经节细胞感受野形成中的相对作用知之甚少。视觉世界的不同特征由10-15种不同的神经节细胞类型提取,然后以不同的处理流发送到大脑。这些不同的神经节细胞的感受野组织可能是独特的形状不同的内部和外部视网膜周围的贡献。神经节细胞感受野也可以通过光适应而改变,但尚不清楚内部和外部视网膜如何促成这些变化。这个提议的目标是确定负责跨神经节细胞发现的感受野多样性的电路和突触机制。电生理学、药理学和解剖学方法将用于确定内部和外部视网膜环绕通路如何在形态上不同的神经节细胞中形成感受野。三个具体目标将确定1)外视网膜在GC感受野组织中的作用,2)确定内视网膜在GC感受野组织中的作用,以及3)确定光适应如何改变内视网膜和外视网膜对GC感受野组织的贡献。通过定义在特定GC类型中介导周围信号的内外丛状层的确切作用,我们将开发一个更完整的图片,空间和对比度信息是如何通过不同的视觉信号通路处理的。
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 }}
PETER D LUKASIEWICZ其他文献
PETER D LUKASIEWICZ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('PETER D LUKASIEWICZ', 18)}}的其他基金
FASEB Summer Conference on Retinal Neurobiology and Visual Processing
FASEB 视网膜神经生物学和视觉处理夏季会议
- 批准号:
7539745 - 财政年份:2008
- 资助金额:
$ 39.47万 - 项目类别:
相似国自然基金
Sitagliptin通过microbiota-gut-brain轴在2型糖尿病致阿尔茨海默样变中的脑保护作用机制
- 批准号:81801389
- 批准年份:2018
- 资助金额:21.0 万元
- 项目类别:青年科学基金项目
平扫描数据导引的超低剂量Brain-PCT成像新方法研究
- 批准号:81101046
- 批准年份:2011
- 资助金额:23.0 万元
- 项目类别:青年科学基金项目
相似海外基金
Resolving the Role of Brain Lymphatic Endothelial Cells in Sleep Dependent Brain Clearance
解决脑淋巴内皮细胞在睡眠依赖性脑清除中的作用
- 批准号:
BB/Y001206/1 - 财政年份:2024
- 资助金额:
$ 39.47万 - 项目类别:
Research Grant
Diversity of neural stem cells lineages and temporal scaling in mammalian complex brain formation
哺乳动物复杂大脑形成中神经干细胞谱系的多样性和时间尺度
- 批准号:
23H00383 - 财政年份:2023
- 资助金额:
$ 39.47万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Therapeutic strategies for sepsis-associated mental disorders focusing on T cells and neurogenesis in the brain.
脓毒症相关精神障碍的治疗策略重点关注大脑中的 T 细胞和神经发生。
- 批准号:
23K08459 - 财政年份:2023
- 资助金额:
$ 39.47万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Phase I study of B7-H3 targeting CAR-T cells administered by local delivery in paediatric high risk brain tumour patients.
B7-H3 靶向 CAR-T 细胞的 I 期研究通过局部递送在儿科高危脑肿瘤患者中进行。
- 批准号:
MR/X030199/1 - 财政年份:2023
- 资助金额:
$ 39.47万 - 项目类别:
Research Grant
The role of vascular immune cells in recovery after brain haemorrhage
血管免疫细胞在脑出血后恢复中的作用
- 批准号:
2897409 - 财政年份:2023
- 资助金额:
$ 39.47万 - 项目类别:
Studentship
Immune cells at the blood-brain interface driving concussion-related symptoms
血脑界面的免疫细胞导致脑震荡相关症状
- 批准号:
2897591 - 财政年份:2023
- 资助金额:
$ 39.47万 - 项目类别:
Studentship
Brain-targeted delivery of therapeutic molecules by exosomes derived from engineered human iPS cells: a potential therapeutic approach for Huntington's disease
通过源自工程化人类 iPS 细胞的外泌体向大脑靶向递送治疗分子:亨廷顿病的潜在治疗方法
- 批准号:
10588392 - 财政年份:2023
- 资助金额:
$ 39.47万 - 项目类别:
Targeting myeloid cells to increase efficacy of immunotherapy against brain tumors.
靶向骨髓细胞以提高针对脑肿瘤的免疫疗法的功效。
- 批准号:
10571040 - 财政年份:2023
- 资助金额:
$ 39.47万 - 项目类别:
Illuminating neurodegenerative tauopathy from somatic genomic landscapes of single human brain cells
从单个人脑细胞的体细胞基因组景观中阐明神经退行性 tau 病
- 批准号:
10686570 - 财政年份:2023
- 资助金额:
$ 39.47万 - 项目类别:
The role of oligodendrocyte precursor cells in circuit remodeling in the mature brain
少突胶质细胞前体细胞在成熟脑回路重塑中的作用
- 批准号:
10750508 - 财政年份:2023
- 资助金额:
$ 39.47万 - 项目类别:














{{item.name}}会员




