Neural coding of interneuron populations in the retina

视网膜中间神经元群的神经编码

基本信息

  • 批准号:
    10225643
  • 负责人:
  • 金额:
    $ 37.6万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2014
  • 资助国家:
    美国
  • 起止时间:
    2014-12-01 至 2023-03-31
  • 项目状态:
    已结题

项目摘要

Abstract The vertebrate retina translates visual images into electrical signals in the optic nerve, initiating the basis of all visual perception. This process is accomplished by dozens of diverse types of interneurons, each of which comprises a population of many thousands of cells. Each of these populations cover the visual field, acting together to process different aspects of visual images. Although many informative studies of retinal neural function have used single cell recordings, understanding the coordinated actions of many cells requires the recording and analysis of cell populations. This proposal focuses on amacrine cells, a diverse population of inhibitory interneurons. In particular we study wide-field amacrine cells, a prominent class of cells that make long distance connections across the retina, acting to combine visual signals from distant locations in the image. We have little information assigning computations to specific cells of this type. Using genetically identified populations of wide-field amacrine cells in the mouse retina, we will record neural activity from these populations optically, along with simultaneously recording electrically from populations of retinal ganglion cells. Neural responses to complex stimuli including natural scenes will be interpreted using advanced computational models. The primary goals of these studies are to 1) perform the first population scale measurements of sparse wide-field amacrine cells, in particular to measure how their selectivity for visual features varies dynamically during natural scenes, 2) Analyze the neural code of these cells under natural scenes using state-of-the-art computational models that can capture retinal responses to arbitrarily complex stimuli, 3) Test the hypothesis that sparse wide-field amacrine cells perform similar computations on different channels of information, acting to remove correlations from the ganglion cell population during natural scenes. These results will have immediate applicability to the emerging field of retinal prostheses, as is used to treat prevalent diseases such as age-related macular degeneration and retinitis pigmentosa by replacing the function of the damaged retina with a high resolution electronic circuit. Measurements of the retinal neural code and the computations that are performed will be directly useful for incorporation into retinal prosthesis systems.
摘要 脊椎动物的视网膜将视觉图像转化为视神经中的电信号,启动视觉信号。 所有视觉感知的基础。这个过程是由几十种不同类型的中间神经元完成的, 每一个细胞都包括数千个细胞的群体。这些人群中的每一个都涵盖了 视觉领域,共同作用,以处理视觉图像的不同方面。虽然许多信息 视网膜神经功能的研究使用单细胞记录,了解协调的 许多细胞的活动需要记录和分析细胞群。该提案的重点是 无长突细胞,一种多样的抑制性中间神经元。特别是我们研究宽场 无长突细胞,一种在视网膜上进行长距离连接的突出细胞, 以联合收割机组合来自图像中远处位置的视觉信号。我们没有什么信息 计算到这种类型的特定细胞。利用遗传鉴定的宽领域种群 无长突细胞在小鼠视网膜,我们将记录这些群体的神经活动光学,沿着 同时对视网膜神经节细胞群进行电记录。Neural responses to 包括自然场景在内的复杂刺激将使用先进的计算模型进行解释。的 这些研究的主要目标是:1)进行稀疏的第一次人口规模测量, 宽视野无长突细胞,特别是测量它们对视觉特征的选择性如何变化 2)分析自然场景下这些细胞的神经代码 使用最先进的计算模型,可以捕捉视网膜反应, 刺激,3)测试稀疏的宽视野无长突细胞对刺激进行类似计算的假设。 不同的信息渠道,作用是从神经节细胞群体中去除相关性, 自然场景。这些结果将立即适用于新兴领域的视网膜 假体,如用于治疗流行疾病,如年龄相关性黄斑变性, 视网膜色素变性通过用高分辨率电子替代受损视网膜的功能, 电路.视网膜神经代码的测量和所执行的计算将是 直接用于结合到视网膜假体系统中。

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 }}

STEPHEN A BACCUS其他文献

STEPHEN A BACCUS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('STEPHEN A BACCUS', 18)}}的其他基金

Neural processing of natural scenes in the visual cortex
视觉皮层自然场景的神经处理
  • 批准号:
    10660753
  • 财政年份:
    2023
  • 资助金额:
    $ 37.6万
  • 项目类别:
Neurostimulation by Ultrasound: Physical Biophysical and Neural Mechanisms
超声神经刺激:物理生物物理和神经机制
  • 批准号:
    10709771
  • 财政年份:
    2020
  • 资助金额:
    $ 37.6万
  • 项目类别:
Advanced Computing/Computational Core
高级计算/计算核心
  • 批准号:
    10213736
  • 财政年份:
    2017
  • 资助金额:
    $ 37.6万
  • 项目类别:
Neurostimulation by Ultrasound: Physical, Biophysical and Neural Mechanisms
超声神经刺激:物理、生物物理和神经机制
  • 批准号:
    8765479
  • 财政年份:
    2014
  • 资助金额:
    $ 37.6万
  • 项目类别:
Neural coding of interneuron populations in the retina
视网膜中间神经元群的神经编码
  • 批准号:
    10380747
  • 财政年份:
    2014
  • 资助金额:
    $ 37.6万
  • 项目类别:
Neural coding of interneuron populations in the retina
视网膜中间神经元群的神经编码
  • 批准号:
    9189613
  • 财政年份:
    2014
  • 资助金额:
    $ 37.6万
  • 项目类别:
Neural coding of interneuron populations in the retina
视网膜中间神经元群的神经编码
  • 批准号:
    8810457
  • 财政年份:
    2014
  • 资助金额:
    $ 37.6万
  • 项目类别:
Function and circuitry of adaptive inhibition in the retina
视网膜适应性抑制的功能和电路
  • 批准号:
    10328505
  • 财政年份:
    2013
  • 资助金额:
    $ 37.6万
  • 项目类别:
Function and circuitry of adaptive inhibition in the retina
视网膜适应性抑制的功能和电路
  • 批准号:
    9292331
  • 财政年份:
    2013
  • 资助金额:
    $ 37.6万
  • 项目类别:
Function and circuitry of adaptive inhibition in the retina
视网膜适应性抑制的功能和电路
  • 批准号:
    8660301
  • 财政年份:
    2013
  • 资助金额:
    $ 37.6万
  • 项目类别:

相似海外基金

I(eye)-SCREEN: A real-world AI-based infrastructure for screening and prediction of progression in age-related macular degeneration (AMD) providing accessible shared care
I(eye)-SCREEN:基于人工智能的现实基础设施,用于筛查和预测年龄相关性黄斑变性 (AMD) 的进展,提供可及的共享护理
  • 批准号:
    10102692
  • 财政年份:
    2024
  • 资助金额:
    $ 37.6万
  • 项目类别:
    EU-Funded
Inhibiting Neovascularization and Subretinal Fibrosis in Neovascular Age-Related Macular Degeneration
抑制新生血管性年龄相关性黄斑变性的新生血管形成和视网膜下纤维化
  • 批准号:
    10639785
  • 财政年份:
    2023
  • 资助金额:
    $ 37.6万
  • 项目类别:
Inhibition of melanogenesis in retinal pigment epithelium, a contributing factor in age-related macular degeneration
抑制视网膜色素上皮中的黑色素生成,这是年龄相关性黄斑变性的一个促成因素
  • 批准号:
    23K09052
  • 财政年份:
    2023
  • 资助金额:
    $ 37.6万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Deciphering the role of osteopontin in the aging eye and age-related macular degeneration
破译骨桥蛋白在眼睛老化和年龄相关性黄斑变性中的作用
  • 批准号:
    10679287
  • 财政年份:
    2023
  • 资助金额:
    $ 37.6万
  • 项目类别:
Evaluation of New Anti-inflammatory Treatments for Age-Related Macular Degeneration
年龄相关性黄斑变性的新型抗炎治疗方法的评价
  • 批准号:
    10642988
  • 财政年份:
    2023
  • 资助金额:
    $ 37.6万
  • 项目类别:
Progression of Early Atrophic Lesions in Age-related Macular degeneration
年龄相关性黄斑变性早期萎缩性病变的进展
  • 批准号:
    10635325
  • 财政年份:
    2023
  • 资助金额:
    $ 37.6万
  • 项目类别:
Cellular and molecular mechanisms of AIM2 and NLRP3 inflammasome activation in age-related macular degeneration
年龄相关性黄斑变性中 AIM2 和 NLRP3 炎症小体激活的细胞和分子机制
  • 批准号:
    10584110
  • 财政年份:
    2023
  • 资助金额:
    $ 37.6万
  • 项目类别:
Elucidation of roles of mast cells and macrophages in the pathogenesis of age-related macular degeneration
阐明肥大细胞和巨噬细胞在年龄相关性黄斑变性发病机制中的作用
  • 批准号:
    22H03243
  • 财政年份:
    2022
  • 资助金额:
    $ 37.6万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
AMD Mitochondria Modulate Expression of microRNA 135b-5p and 148a-3p in RPE Cybrids: Implications for Age-related Macular Degeneration
AMD 线粒体调节 RPE Cybrids 中 microRNA 135b-5p 和 148a-3p 的表达:对年龄相关性黄斑变性的影响
  • 批准号:
    10433610
  • 财政年份:
    2022
  • 资助金额:
    $ 37.6万
  • 项目类别:
Targeting the inflammatory response in age-related macular degeneration
针对年龄相关性黄斑变性的炎症反应
  • 批准号:
    10504138
  • 财政年份:
    2022
  • 资助金额:
    $ 37.6万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了