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Our broad objective is to understand the mechanisms by which the nerve growth factor (NGF) signal is propagated from the axon terminal to the cell body. NGF retrograde signaling is critical for the survival, differentiation, and maintenance of certain types neurons. Disrupted NGF retrograde transport was reported to contribute to the loss of the basal forebarin cholinergic (BFC) neurons in the brains of patients with Alzheimer's Disease or Down's Syndrome. This project will use advanced imaging techniques to directly visualize NGF transport in live neruons in real time. We focus on exploring dynamic features of NGF transport in normal and Down's Syndrome mice. The aims are: 1. Characterize the movement of NGF-containing endosomes in axons and define their pausing mechanism(s), by using quantum dot conjugated NGF to track endosomal movements with nanometer resolution. 2. Determine whether NGF-lacking endosomes are present, whether they are relevant for NGF signaling, and whether there are alternative signaling pathways independent of endosomal transport, by marking the NGF-lacking endosomes with photo-activatable green fluorescence proteins that are fused to the C-terminal of TrkA receptor. 3. Identify the abnormal features of disrupted NGF transport in Down Syndrome mouse neurons, by characterizing individual features of transport dynamics, which inlcude the average speed, the moving speed, the pausing duration, and the pausing frequency. 4. Determine how amyloid precursor protein overexpression leads to the abnormal NGF retrograde transport in Down Syndrome mouse by examining how overexpression of amyloid precursor protein in DS mice might cause defective structural or axonal features that lead to disrupted NGF transport. Achieving those aims will increase our understanding of how NGF signal is propagated in normal and degenerative neurons. More broadly, those studies will contribute to elucidate the pathogenesis of Alzheimer's disease and Down syndrome.
期刊论文(7)
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会议论文
DOI: 10.1039/c2ib20062g
发表时间: 2012-08
期刊: Integrative biology : quantitative biosciences from nano to macro
影响因子: --
作者: [Xie W, Zhang K, Cui B]
通讯作者: Cui B
DOI: 10.1039/c003385e
发表时间: 2010-10-07
期刊: Lab on a chip
影响因子: 6.1
作者: [Zhang K, Osakada Y, Vrljic M, Chen L, Mudrakola HV, Cui B]
通讯作者: Cui B
DOI: 10.1021/nl101950x
发表时间: 2010-10-13
期刊: Nano letters
影响因子: 10.8
作者: [Xie C, Hanson L, Xie W, Lin Z, Cui B, Cui Y]
通讯作者: Cui Y
DOI: 10.1021/acs.langmuir.6b03903
发表时间: 2017-01-31
期刊: Langmuir : the ACS journal of surfaces and colloids
影响因子: --
作者: [Lou HY, Zhao W, Hanson L, Zeng C, Cui Y, Cui B]
通讯作者: Cui B
An electrophysiology platform that enables robust, scalable and long-term intracellular recording of cardiomyocytes
  • 批准号:
    10500961
  • 项目类别:
  • 资助金额:
    $47.66万
  • 财政年份:
    2022
  • 负责人:
    Bianxiao Cui
  • 依托单位:
An electrophysiology platform that enables robust, scalable and long-term intracellular recording of cardiomyocytes
  • 批准号:
    10641918
  • 项目类别:
  • 资助金额:
    $58.86万
  • 财政年份:
    2022
  • 负责人:
    Bianxiao Cui
  • 依托单位:
Label-free Optical Recording of Neuroelectric Activities
  • 批准号:
    10190148
  • 项目类别:
  • 资助金额:
    $43.41万
  • 财政年份:
    2021
  • 负责人:
    Bianxiao Cui
  • 依托单位:
Label-free Optical Recording of Neuroelectric Activities
  • 批准号:
    10361478
  • 项目类别:
  • 资助金额:
    $46.54万
  • 财政年份:
    2021
  • 负责人:
    Bianxiao Cui
  • 依托单位:
国内基金
海外基金
新型F-18标记香豆素衍生物PET探针的研制及靶向Alzheimer's Disease 斑块显像研究
  • 批准号:
    81000622
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    20.0万元
  • 批准年份:
    2010
  • 负责人:
    梁胜
  • 依托单位:
阿尔茨海默病(Alzheimer's disease,AD)动物模型构建的分子机理研究
  • 批准号:
    31060293
  • 项目类别:
    地区科学基金项目
  • 资助金额:
    26.0万元
  • 批准年份:
    2010
  • 负责人:
    郭亚芬
  • 依托单位:
跨膜转运蛋白21(TMP21)对引起阿尔茨海默病(Alzheimer'S Disease)的γ分泌酶的作用研究