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PROJECT SUMMARY/ABSTRACT The cerebral cortex mediates all of human and animal cognition, encompassing a diverse set of abilities including sensation, perception, decision making, and motor planning. Dysfunctions of the cerebral cortex are thought to underlie numerous neurological and psychiatric disorders. A major obstacle both to understanding normal behaving and to treating pathology is the high degree of complexity of cortical circuitry, which has remained largely enigmatic. The conventional view of neocortex has been that sensory processing begins in layer 4 (L4), which was identified a century ago as the principal target of thalamic axons carrying information from our sensory organs. Sensory transforms are widely believed to occur as excitation spreads serially along the densest axonal pathways (thalamus→L4→L2/3→L5/6). Recently we discovered that the cerebral cortex, rather than being a monolithic structure, may contain two entirely separate processing systems, activated by the same signals arising from the thalamus. L4 is thus not an obligatory distribution hub for cortical activity, and thalamus activates two distinct “strata” of cortex in parallel. This proposal's goal is to identify the behavioral and computational roles of the upper (L2-4) and lower strata (L5/6) as well as the interactions between them. We will investigate the behavioral roles of these layers in the mouse whisker system. Specific layers will be optogenetically disrupted in a series of tactile behavioral tasks, in which task complexity is progressively increased. Interlaminar interactions will also be studied by recording electrophysiologically from specific layers during behavior and using novel machine learning techniques designed to identify the type of computation performed in different levels of “deep networks”. The dimensionality of the representation in a layer will be estimated under normal behaviors and when specific layers are inactivated. Identifying fundamental functions of upper versus cortical layers will likely pave the way for future studies in other neocortical systems and in higher-order species. Moreover, as the different layers contain molecularly and biophysically distinct cell types and project to distinct downstream targets, specific neurological disorders may involve dysfunction of specific pathways, cell types, and layers. Establishing the behavioral and computational roles of these elements may contribute to development of targeted therapies.
期刊论文(3)
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科研奖励(0)
会议论文
High-order thalamic inputs to primary somatosensory cortex are stronger and longer lasting than cortical inputs.
初级体感皮层的高阶丘脑输入比皮层输入更强、更持久。
DOI: 10.7554/elife.44158
发表时间: 2019
期刊: eLife
影响因子: 7.7
作者: [Zhang,Wanying, Bruno,RandyM]
通讯作者: Bruno,RandyM
DOI: 10.1038/s41467-022-33141-y
发表时间: 2022-09-20
期刊: Nature communications
影响因子: 16.6
作者: []
通讯作者:
Brain control of internal organ function
  • 批准号:
    10679652
  • 项目类别:
  • 资助金额:
    $118.82万
  • 财政年份:
    2021
  • 负责人:
    Rui M. Costa
  • 依托单位:
Brain control of internal organ function
  • 批准号:
    10703497
  • 项目类别:
  • 资助金额:
    $114.83万
  • 财政年份:
    2021
  • 负责人:
    Rui M. Costa
  • 依托单位:
Brain control of internal organ function
2020 Basal Ganglia Gordon Research Conference and Gordon Research Seminar
  • 批准号:
    9912902
  • 项目类别:
  • 资助金额:
    $1.5万
  • 财政年份:
    2019
  • 负责人:
    Rui M. Costa
  • 依托单位:
国内基金
海外基金
层出镰刀菌氮代谢调控因子AreA 介导伏马菌素 FB1 生物合成的作用机理
  • 批准号:
    2021JJ40433
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2021
  • 负责人:
    孙磊
  • 依托单位:
寄主诱导梢腐病菌AreA和CYP51基因沉默增强甘蔗抗病性机制解析
  • 批准号:
    32001603
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    24.0万元
  • 批准年份:
    2020
  • 负责人:
    段真珍
  • 依托单位:
AREA国际经济模型的移植.改进和应用
  • 批准号:
    18870435
  • 项目类别:
    面上项目
  • 资助金额:
    2.0万元
  • 批准年份:
    1988
  • 负责人:
    史树中
  • 依托单位: