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中文摘要
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描述(由申请人提供):黑视素是一种假定的光色素,最近被证明存在于大鼠和小鼠的一小部分(1-2%)内在光敏的视网膜神经节细胞中。这些细胞投射到大脑中非图像形成的视觉中心,如视交叉上核、束间小叶和橄榄叶前核。本研究的长期目标是详细了解黑视素相关视觉通路的结构和功能。具体目标是:
英文摘要
DESCRIPTION (provided by applicant): Melanopsin is a putative photopigment recently shown to be present in a small subset (1-2%) of intrinsically photosensitive retinal ganglion cells in rat and mouse. These cells project to non-image-forming visual centers in the brain, such as the suprachiasmatic nucleus, the intergeniculate leaflet and the olivary pretectal nucleus. The long-term objective of this proposal is to understand the structure and function of the melanopsin-associated visual pathway in detail. The specific aims are: 1) To map the projections of the melanopsin-containing retinal ganglion cells to the mouse brain in detail, 2) To assess the contribution of melanopsin-associated signaling versus that of rod/cone signaling to non-image-forming visual functions in mouse, 3) To study the light responses and the phototransduction mechanism of the intrinsically photosensitive, melanopsin-expressing retinal ganglion cells, and 4) To study the characteristics of the melanopsin-expressing retinal neurons in primates and other vertebrates. The experimental approach will combine mouse genetics, cell biology, electrophysiology and some collaborative whole-animal physiological and behavioral experiments.
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Melanopsin Photoreception and Signaling
  • 批准号:
    10438306
  • 项目类别:
  • 资助金额:
    $40.94万
  • 财政年份:
    2022
  • 负责人:
    KING-WAI YAU
  • 依托单位:
Melanopsin Photoreception and Signaling
  • 批准号:
    10630285
  • 项目类别:
  • 资助金额:
    $40.94万
  • 财政年份:
    2022
  • 负责人:
    KING-WAI YAU
  • 依托单位:
Cyclic AMP- and Ca2+-Signaling in Sensory Transduction by Olfactory Receptor Neurons
  • 批准号:
    10443371
  • 项目类别:
  • 资助金额:
    $40.94万
  • 财政年份:
    2015
  • 负责人:
    KING-WAI YAU
  • 依托单位:
Cyclic AMP- and Ca2+-Signaling in Sensory Transduction by Olfactory Receptor Neurons
  • 批准号:
    10622600
  • 项目类别:
  • 资助金额:
    $40.94万
  • 财政年份:
    2015
  • 负责人:
    KING-WAI YAU
  • 依托单位:
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