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This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Objective: The long-term objectives of this proposal are to understand the functional organization of feedforward and feedback pathways between the lateral geniculate nucleus (LGN) and visual cortex. For sensory systems, feedforward projections from thalamic relay cells provide the cortex with information about the external environment. The cortex, in turn, sends extensive feedback to thalamic relay cells. The cortex thus functions both to process information supplied by the thalamus as well as to influence dynamically the transmission of thalamic input. The proposed studies involve three sets of experiments. The first set of experiments deals with the issue of what role magnocellular and parvocellular LGN inputs play in the construction of postsynaptic receptive fields in layer 4C of visual cortex. Recordings will be made from monosynaptically connected neurons in the LGN and layer 4C in order to compare the organization of pre- and postsynaptic receptive fields as well as to assess the dynamics of synaptic transmission. The second set of experiments deals with determining the physiology of corticogeniculate feedback neurons located in layer 6 of visual cortex. Neurons in layer 6 that provide feedback input to the LGN are located in the upper third and lower third of the layer. Neurons in the upper third project exclusively to the parvocellular geniculate layers; neurons in the lower third project primarily to the magnocellular layers. We will examine the physiological properties of these neurons to determine whether they are differentially sensitive to visual stimuli. If so, then it seems likely that neurons in the upper and lower regions of layer 6 should be able to differentially modulate activity traveling in the magno- and parvocellular streams. The third set of experiments deals with the functional influence of cortical feedback on geniculate activity. By recording from ensembles of geniculate neurons, we will determine whether cortical feedback selectively influences the activity of neurons in the magno- and parvocellular layers of the LGN. If feedback is found to influence the temporal patterns of LGN activity, then we will examine data from the first set of experiments to determine the efficacy of these patterns in driving cortical responses.
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Pulvinar cellular and network dynamics in cognitive control of sensory processes.
  • 批准号:
    10633806
  • 项目类别:
  • 资助金额:
    $48.52万
  • 财政年份:
    2023
  • 负责人:
    W MARTIN USREY
  • 依托单位:
UC Davis Advancing Diversity in the Neuroscience Research (ADNR) Program
UC Davis Advancing Diversity in the Neuroscience Research (ADNR) Program
UC Davis Advancing Diversity in the Neuroscience Research (ADNR) Program
国内基金
海外基金
分化肌细胞脱细胞ECM-cells sheet 3D 支架构建及其促进容积性肌组织缺损再 生修复应用及机制研究
CAFs-TAMs-tumor cells调控在HRHPV感染致癌中的作用机制研究及AI可追溯预测模型建立
  • 批准号:
    82072862
  • 项目类别:
    面上项目
  • 资助金额:
    56.0万元
  • 批准年份:
    2020
  • 负责人:
    徐云升
  • 依托单位:
S100A8/A9--Myeloid cells特异性可溶性表氧化物水解酶(sEH)基因敲除改善胰岛素抵抗的新靶点
  • 批准号:
    82070825
  • 项目类别:
    面上项目
  • 资助金额:
    53.0万元
  • 批准年份:
    2020
  • 负责人:
    徐西振
  • 依托单位:
Leader cells通过CCL5调控糖酵解及基质硬度促进结直肠癌集体侵袭的 作用机制
  • 批准号:
    81903002
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    20.5万元
  • 批准年份:
    2019
  • 负责人:
    王斐斐
  • 依托单位: