Molecular mechanisms of the neuronal migration in the brain

大脑神经元迁移的分子机制

基本信息

  • 批准号:
    12480239
  • 负责人:
  • 金额:
    $ 6.85万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
  • 财政年份:
    2000
  • 资助国家:
    日本
  • 起止时间:
    2000 至 2001
  • 项目状态:
    已结题

项目摘要

The neurons of the precerebellar nuclei, which include the pontine nuclei (PN), the external cuneatus nucleus (ECN), the lateral reticular nucleus (LRN), and the inferior olivary nucleus (ION), are all generated from lower rhombic lips (dorsal rims of the medulla) at different periods. They then migrate tangentially and finally stop their proper positions ipsilaterally (PN and ION) or contralaterally (ECN and LRN) to the ventral midline, floor plate (FP). The features of their migrations raise some questions about how they migrate tangentially ; why do some of them cross the FP, but the others not ; how do they find their correct positions. To begin to answer these questions, we have made an attempt to reconstitute the precerebellar neuronal migration in vitro. We adopted the flat-whole mount explant culture of the medulla in combination with the transplantation of lower rhombic lip from the transgenic rat that expresses GFP in all tissues to visualize the migrating neurons in in vivo-like environment. After 2 days in culture, many GFP-positive neurons with a long leading process migrating out into the host explant were observed. Most of these cells took a tangential path toward the FP as they do in vivo. Immunostaining also showed that they express TAG-1 and DCC. After 3 days, some of them crossed the FP and continued to migrate. These neurons were initially attracted by the floor plate (FP) at the ventral midline. However, after crossing the midline, they lost their responsiveness to the FP and became attracted by the alar plate (AP). These results identify a crucial change in the response of migrating cells to attractive guidance cues during the transmedian migration of precerebellar neurons.
小脑前核的神经元,包括桥核(PN)、楔外核(ECN)、外侧网状核(LRN)和下橄榄核(ION),都是在不同时期从下菱形嘴唇(延髓背缘)产生的。然后,它们沿切线移动,最终停止其正确的位置,即同侧(PN和Ion)或对侧(ECN和LRN)到腹中线底板(FP)。他们迁徙的特点提出了一些问题:他们是如何切线迁徙的;为什么他们中的一些人越过了FP,而另一些人没有;他们如何找到正确的位置。为了开始回答这些问题,我们试图在体外重建小脑前神经元的迁移。我们采用了延髓的平面-整体贴片培养,并结合表达GFP的转基因大鼠下菱形嘴唇的移植,在类活体环境中显示了迁移的神经元。培养2天后,可见大量GFP阳性神经元向宿主外植体内迁移,并有较长的前导突起。这些细胞中的大多数都像在体内一样,沿着切线路径走向FP。免疫组织化学染色也显示它们表达TAG-1和DCC。3天后,他们中的一些人越过FP继续迁徙。这些神经元最初被腹中线的底板(FP)吸引。然而,在越过中线后,他们失去了对FP的反应性,并被翼板(AP)所吸引。这些结果表明,在小脑前神经元的跨中间迁移过程中,迁移细胞对吸引人的引导线索的反应发生了关键的变化。

项目成果

期刊论文数量(66)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Otsuka, T.: "Excitatory postsynaptic potentials trigger a plateau potential in rat subthalamic neurons at hyperpolarized states"J.Neurophysiol.. 86. 1816-1825 (2001)
Otsuka, T.:“兴奋性突触后电位在超极化状态下触发大鼠底丘脑神经元的平台电位”J.Neurophysiol.. 86. 1816-1825 (2001)
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    0
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Tashiro,Y.: "Afferents of cranial sensory ganglia pathfind of their target independent of the site of entry into the hindbrain."J.Comp.Neurol.. 417. 491-500 (2000)
Tashiro,Y.:“颅感觉神经节的传入神经节独立于进入后脑的位置寻找其目标。”J.Comp.Neurol.. 417. 491-500 (2000)
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    0
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Yamamoto, N.: "Inhibitory mechanism by polysialic acid for lamina-specific branch formation of thalamocortical axons"J. Neurosci.. 20. 9145-9151 (2000)
Yamamoto,N.:“聚唾液酸对丘脑皮质轴突的椎板特异性分支形成的抑制机制”J。
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  • 发表时间:
  • 期刊:
  • 影响因子:
    0
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  • 通讯作者:
Sawamoto, K.: "Visualization, direct isolation, and transplantation of midbrain dopaminergic neurons labeled with a TH-GFP transgene"Proc. Natl. Acad. Sci. USA 98 Å@. 6423-6428 (2001)
Sawamoto,K.:“用 TH-GFP 转基因标记的中脑多巴胺能神经元的可视化、直接分离和移植”,Acad. USA 98 Å@。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Otsuka, T.: "Excitatory postsynaptic potentials trigger a plateau potential in rat subthalamic neurons at hyperpolarized states"J. Neurophysiol.. 86. 1816-1825 (2001)
Otsuka, T.:“兴奋性突触后电位在超极化状态下触发大鼠丘脑底神经元的平台电位”J.
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    0
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MURAKAMI Fujio其他文献

MURAKAMI Fujio的其他文献

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{{ truncateString('MURAKAMI Fujio', 18)}}的其他基金

Origin and fate of earliest generated cortical neurons
最早产生的皮质神经元的起源和命运
  • 批准号:
    24650166
  • 财政年份:
    2012
  • 资助金额:
    $ 6.85万
  • 项目类别:
    Grant-in-Aid for Challenging Exploratory Research
Environmental influence on embryonic brain development
环境对胚胎大脑发育的影响
  • 批准号:
    22659199
  • 财政年份:
    2010
  • 资助金额:
    $ 6.85万
  • 项目类别:
    Grant-in-Aid for Challenging Exploratory Research
Role of neuronal migration for the formation of neuronal connections
神经元迁移对神经元连接形成的作用
  • 批准号:
    17023028
  • 财政年份:
    2005
  • 资助金额:
    $ 6.85万
  • 项目类别:
    Grant-in-Aid for Scientific Research on Priority Areas
Regionalization of developing brain and neuronal migration
发育中的大脑和神经元迁移的区域化
  • 批准号:
    14208095
  • 财政年份:
    2002
  • 资助金额:
    $ 6.85万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Molecular mechanisms of the formation of crossed projetions.
交叉投影形成的分子机制。
  • 批准号:
    09044305
  • 财政年份:
    1997
  • 资助金额:
    $ 6.85万
  • 项目类别:
    Grant-in-Aid for international Scientific Research
Molecular mechanism of axonal regeneration-Role of receptor of repulsive factor for neurite elongation-
轴突再生的分子机制-神经突伸长排斥因子受体的作用-
  • 批准号:
    06454699
  • 财政年份:
    1994
  • 资助金额:
    $ 6.85万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)
Inhibition of Cell Attachment and Neurite Outgrowth by the Factors in Abult CNS White Matter : a Studbstrata.
成体中枢神经系统白质中的因素对细胞附着和神经突生长的抑制:一个 Studbstrata。
  • 批准号:
    01480126
  • 财政年份:
    1989
  • 资助金额:
    $ 6.85万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)
Molecular mechanisms for abnormal development of the brain
大脑异常发育的分子机制
  • 批准号:
    62570425
  • 财政年份:
    1987
  • 资助金额:
    $ 6.85万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)

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    10512459
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    10444843
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剖析 DNA 甲基转移酶 3A (DNMT3A) 突变对神经元细胞命运规范的影响。
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    476693
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逆转三种共济失调常见的神经元细胞脆弱性:克里斯蒂安森综合征、常染色体隐性遗传的沙格奈痉挛性共济失调 (ARSACS) 和脊髓小脑性共济失调 6 型 (SCA6)
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    498209
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    2022
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    Studentship Programs
RNA Regulatory Networks in Neuronal Cell Type Diversity and Function
神经元细胞类型多样性和功能中的 RNA 调控网络
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    10816681
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    2022
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Roles of Chromatin Regulation in Specification of Neuronal Cell Identity
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    Discovery Grants Program - Individual
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    10646306
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Mechanisms of Glial Interactions and Function at Neuronal Cell Bodies
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