Mechanisms of Motion Detection in Retinal Neural Network
视网膜神经网络运动检测机制
基本信息
- 批准号:10752012
- 负责人:
- 金额:$ 46.3万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2018
- 资助国家:美国
- 起止时间:2018-09-30 至 2028-06-30
- 项目状态:未结题
- 来源:
- 关键词:AccelerationAcetylcholineAffectAmacrine CellsAnimalsCalciumCellsCodeComputer ModelsComputer SimulationDendritesDetectionDiameterEnvironmental ImpactEnvironmental Risk FactorFeedbackImageImmunohistochemistryKnowledgeLightMediatingMolecularMotionMusNeural RetinaNeuronsNeurotransmittersNicotinic ReceptorsOutcomePathway interactionsPresynaptic TerminalsReactionReaction TimeRetinaSignal TransductionSpeedStimulusTestingTissuesVisualbehavioral studycholinergicganglion cellmetermotion sensitivityneural networkneurotransmissionobject motionpatch clampreceptive fieldretinal neuronsignal processingstarburst amacrine celltwo-photon
项目摘要
Abstract
Detection of moving objects is a retinal function which is crucial for an animal's survival. Multiple neurons and
neural networks in the retina have been identified as critical players in this task, including starburst amacrine
cells (SACs) and direction-selective ganglion cells (DSGCs), which sense direction of motion. Recent studies
have revealed that several neural networks among bipolar and amacrine cells are involved in direction
selectivity. However, the impact of environmental factors on motion sensitivity tuning of these neurons is not
well understood. Background scenery affects the gain control and tuning of neurons for object motion
detection; however, we have just begun to understand the sensitization and adaptation of those neurons. The
long-term objective of the present project is to understand the cellular and molecular mechanisms in the retina
for sensing direction of motion. We will conduct patch clamp recordings, two-photon calcium imaging,
immunohistochemistry, computational simulation, and behavioral studies to examine the mechanisms
underlying direction selectivity. We previously found that cholinergic feedback from SACs to bipolar cells
contributes to SAC direction selectivity. We now have evidence that the cholinergic feedback is transferred for
a long distance and tune SAC direction selectivity. Therefore, we hypothesize that an incoming object send a
signal to bipolar cells through a cholinergic pathway to tune SAC direction selectivity, a form of predictive
coding. We propose two Specific Aims to investigate long-distance cholinergic feedback. We will test this
hypothesis by recording long-distance cholinergic feedback in bipolar cells (Aim 1), and we will examine the
outcome of the long-distance cholinergic feedback in bipolar cell axon terminals, SAC dendrites, and DSGC
activity (Aim 2). Visual prediction is an essential feature for motion detection, which would reduce neural signal
delays and facilitate the animal reaction. Knowledge gained from the results of this project will shed light on the
additional layer of motion detection and visual signal processing in the retina.
摘要
对运动物体的检测是一种视网膜功能,它对动物的生存至关重要。多个神经元,
视网膜中的神经网络已被确定为这项任务的关键参与者,包括星爆无长突神经网络。
细胞(SAC)和方向选择性神经节细胞(DSGCs),它们感知运动方向。最近的研究
已经揭示了双极细胞和无长突细胞之间的几个神经网络参与了方向,
选择性然而,环境因素对这些神经元的运动敏感性调谐的影响并不明显。
很好理解。背景景物影响目标运动神经元的增益控制和调谐
然而,我们刚刚开始了解这些神经元的敏感性和适应性。的
本项目的长期目标是了解视网膜中的细胞和分子机制
用于感测运动方向。我们将进行膜片钳记录,双光子钙成像,
免疫组织化学、计算机模拟和行为学研究,以检查机制
潜在的方向选择性。我们以前发现,从SAC到双极细胞的胆碱能反馈
有助于SAC方向选择性。我们现在有证据表明,胆碱能反馈被转移到
长距离和调谐SAC方向选择性。因此,我们假设一个传入的对象发送一个
通过胆碱能途径向双极细胞发出信号,以调节SAC方向选择性,这是一种预测
编码我们提出了两个具体的目的来研究长距离胆碱能反馈。我们将测试这个
通过记录双极细胞中的长距离胆碱能反馈(Aim 1),我们将研究
双极细胞轴突终末、SAC树突和DSGC中长距离胆碱能反馈的结果
活动(目标2)。视觉预测是运动检测的一个重要特征,它会减少神经信号
延迟和促进动物反应。从该项目的结果中获得的知识将有助于了解
视网膜中的运动检测和视觉信号处理的附加层。
项目成果
期刊论文数量(7)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
ON and OFF Signaling Pathways in the Retina and the Visual System.
视网膜和视觉系统中的开和关信号通路。
- DOI:10.3389/fopht.2022.989002
- 发表时间:2022
- 期刊:
- 影响因子:0
- 作者:Ichinose,Tomomi;Habib,Samar
- 通讯作者:Habib,Samar
Using Looming Visual Stimuli to Evaluate Mouse Vision.
- DOI:10.3791/59766
- 发表时间:2019-06
- 期刊:
- 影响因子:0
- 作者:Christina C. Koehler;Leo M Hall;Chase B. Hellmer;T. Ichinose
- 通讯作者:Christina C. Koehler;Leo M Hall;Chase B. Hellmer;T. Ichinose
Patch clamp recording from bipolar cells in the wholemount mouse retina.
- DOI:10.1016/j.xpro.2022.101482
- 发表时间:2022-09-16
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Presynaptic depolarization differentially regulates dual neurotransmitter release from starburst amacrine cells in the mouse retina.
突触前去极化差异调节小鼠视网膜星爆无长突细胞的双重神经递质释放。
- DOI:10.3389/fopht.2023.1225824
- 发表时间:2023
- 期刊:
- 影响因子:0
- 作者:Ichinose,Tomomi;Hellmer,ChaseB;Bohl,JeremyM
- 通讯作者:Bohl,JeremyM
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Tomomi Ichinose其他文献
Tomomi Ichinose的其他文献
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{{ truncateString('Tomomi Ichinose', 18)}}的其他基金
ON and OFF visual signaling in the retinal interneurons
视网膜中间神经元中的ON和OFF视觉信号
- 批准号:
10275590 - 财政年份:2021
- 资助金额:
$ 46.3万 - 项目类别:
ON and OFF visual signaling in the retinal interneurons
视网膜中间神经元中的ON和OFF视觉信号
- 批准号:
10456209 - 财政年份:2021
- 资助金额:
$ 46.3万 - 项目类别:
ON and OFF visual signaling in the retinal interneurons
视网膜中间神经元中的ON和OFF视觉信号
- 批准号:
10610970 - 财政年份:2021
- 资助金额:
$ 46.3万 - 项目类别:
Mechanisms of Motion Detection in Retinal Neural Network
视网膜神经网络运动检测机制
- 批准号:
10058854 - 财政年份:2018
- 资助金额:
$ 46.3万 - 项目类别:
Mechanisms of Motion Detection in Retinal Neural Network
视网膜神经网络运动检测机制
- 批准号:
10164792 - 财政年份:2018
- 资助金额:
$ 46.3万 - 项目类别:
MECHANISMS OF TEMPORAL ENCODING IN RETINAL BIPOLAR CELLS
视网膜双极细胞的时间编码机制
- 批准号:
8300076 - 财政年份:2011
- 资助金额:
$ 46.3万 - 项目类别:
MECHANISMS OF TEMPORAL ENCODING IN RETINAL BIPOLAR CELLS
视网膜双极细胞的时间编码机制
- 批准号:
8738102 - 财政年份:2011
- 资助金额:
$ 46.3万 - 项目类别:
MECHANISMS OF TEMPORAL ENCODING IN RETINAL BIPOLAR CELLS
视网膜双极细胞的时间编码机制
- 批准号:
8530235 - 财政年份:2011
- 资助金额:
$ 46.3万 - 项目类别:
MECHANISMS OF TEMPORAL ENCODING IN RETINAL BIPOLAR CELLS
视网膜双极细胞的时间编码机制
- 批准号:
8106973 - 财政年份:2011
- 资助金额:
$ 46.3万 - 项目类别:
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