课题基金 / 基金详情

How early eye circuits process and present visual features

How early eye circuits process and present visual features
早期眼回路如何处理和呈现视觉特征
批准号:
BB/M009564/1
负责人:
Mikko Ilmari Juusola
金额:
$115.94万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2015
资助国家:
英国
项目状态:
已结题
起止时间:
2015 至 --

项目摘要

项目成果

Mikko Ilmari Juusola的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
From humans to fruit flies, the ability of resolve individual objects by their features and to link these features to a coherent precept of the world is crucial for visual behaviours and fitness of seeing animals. But it remains a mystery how information processing within the networks of nerve cells in the eyes make object recognition possible.Eye circuits process and represent visual information as patterns. Some of these patterns are complex and allow the brain, for example, to recognize objects from different perspectives. It is not understood how the eyes/brains represent visual information as patterns, recognises those patterns, and then solves problems. However, it is likely that the underlying processes occur at the level of circuits, where neurons and their connections interact dynamically. These important questions have direct implications for how we understand neural mechanisms for object/pattern recognition, with obvious links to artificial visual systems, machine-learning and robotics. Yet remarkably, they can be particularly well studied in the simple eyes and brain of fruit fly, Drosophila. While fly and human eyes have a very different architecture, both eyes must somehow extract object features from visual scenes, and to link these neural representations to some form of internal activity "maps" to execute goal-oriented behaviours. Importantly, Drosophila has a hard-wired circuitry of known layout, genetic toolboxes for modifying connectivity, and allows monitoring of neural activity with scalable resolution during visual stimulation/behaviour. This would not be possible in human eyes/brain. We now wish to utilise new wiring diagrams, genetic, electrophysiological and optical imaging tools available for Drosophila and state of the art mathematical analysis to study neural mechanisms of object representation at the level of its eye microcircuits. Specifically, we are interested in uncovering what kind of processing strategies early visual circuits use to extract object features; how and why eye circuits separate and integrate the representations of object colour and shape ('what' information) from that of its location and motion ('where' information), and how these representations adapt when the same object is seen in different lighting conditions/backgrounds. This research plan aims to start identifying and quantifying the fundamental early neural mechanisms for object perception that are probably used in the nervous systems of seeing animals across the animal kingdom. The knowledge we gain from these studies will not only advance our understanding of how animals see but, because the basic underlying neural connectivity and synaptic mechanisms are so widely found in other sensory systems and in our brain, will provide new insight into many other, often clinically important processes in the nervous system. Thus, our results should be off great interest to academics and industry, seeking to understand biologically-inspired design for machine sensing; principles which are usually more robust, cheaper, smaller and more energy-efficient than conventional engineering concepts. In long term, the new knowledge from our experiments and modelling may even help to manufacture novel adaptive biochips and test their performance as sensory implants.
期刊论文(10)
专著(0)
科研奖励(0)
会议论文
DOI: 10.7554/elife.26117
发表时间: 2017-09-05
期刊: eLife
影响因子: 7.7
作者: [Juusola M, Dau A, Song Z, Solanki N, Rien D, Jaciuch D, Dongre SA, Blanchard F, de Polavieja GG, Hardie RC, Takalo J]
通讯作者: Takalo J
DOI: 10.1101/2020.12.14.422675
发表时间: 2020-12
期刊: bioRxiv
影响因子: --
作者: [David Jaciuch;J. Munns;S. Chawla;S. Davis;M. Juusola]
通讯作者: David Jaciuch;J. Munns;S. Chawla;S. Davis;M. Juusola
Encyclopedia of Computational Neuroscience
计算神经科学百科全书
DOI: 10.1007/978-1-4614-6675-8_333
发表时间: 2015
期刊:
影响因子: --
作者: [Juusola M]
通讯作者: Juusola M
DOI: 10.1113/jp273645
发表时间: 2017-08-15
期刊: The Journal of physiology
影响因子: --
作者: [Juusola M, Song Z]
通讯作者: Song Z
8
    2022BBSRC-NSF/BIO Generating New Network Analysis Tools for Elucidating the Functional Logic of 3D Vision Circuits of the Drosophila Brain
    • 批准号:
      BB/Y000234/1
    • 项目类别:
      Research Grant
    • 资助金额:
      $107.95万
    • 财政年份:
      2024
    • 负责人:
      Mikko Ilmari Juusola
    • 依托单位:
    New insight into functional eye evolution: seeing the world through moving photoreceptors.
    • 批准号:
      BB/X006247/1
    • 项目类别:
      Research Grant
    • 资助金额:
      $85.01万
    • 财政年份:
      2023
    • 负责人:
      Mikko Ilmari Juusola
    • 依托单位:
    Insect-inspired depth perception
    • 批准号:
      EP/X019705/1
    • 项目类别:
      Research Grant
    • 资助金额:
      $69.84万
    • 财政年份:
      2023
    • 负责人:
      Mikko Ilmari Juusola
    • 依托单位:
    How does the Drosophila brain compute and see visual motion?
    • 批准号:
      BB/F012071/1
    • 项目类别:
      Research Grant
    • 资助金额:
      $69.45万
    • 财政年份:
      2008
    • 负责人:
      Mikko Ilmari Juusola
    • 依托单位:
    国内基金
    海外基金
    Crocin 抑制 Hartley 豚鼠早期骨关节炎发生的 作用机制研究
    RIPK3蛋白及其RHIM结构域在脓毒症早期炎症反应和脏器损伤中的作用和机制研究
    • 批准号:
      82372167
    • 项目类别:
      面上项目
    • 资助金额:
      48.00万元
    • 批准年份:
      2023
    • 负责人:
      江继宏
    • 依托单位:
    均相液相生物芯片检测系统的构建及其在癌症早期诊断上的应用
    • 批准号:
      82372089
    • 项目类别:
      面上项目
    • 资助金额:
      48.00万元
    • 批准年份:
      2023
    • 负责人:
      李万万
    • 依托单位:
    环境抗雄激素干预AR/TGFB1I1致尿道下裂血管内皮细胞发育异常的机制及其“预警信号”在早期诊断中的价值
    • 批准号:
      82371605
    • 项目类别:
      面上项目
    • 资助金额:
      46.00万元
    • 批准年份:
      2023
    • 负责人:
      蒋君涛
    • 依托单位: