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Common and distinct mechanisms for ARF6-mediated neuronal migration and cancer invasion

Common and distinct mechanisms for ARF6-mediated neuronal migration and cancer invasion
ARF6 介导的神经元迁移和癌症侵袭的常见和独特机制
批准号:
23659101
负责人:
SAKAGAMI Hiroyuki
金额:
$2.41万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Challenging Exploratory Research
财政年份:
2011
资助国家:
日本
项目状态:
已结题
起止时间:
2011 至 2012

项目摘要

项目成果

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中文摘要
翻译
ADP核糖化因子是一种小的GTP酶,通过激活脂质修饰酶和募集各种相互作用的蛋白如FIP3/4和JIP3/4来调节膜运输和肌动蛋白重塑。最近的证据表明,ARF6通路在肿瘤侵袭和转移等细胞运动中具有重要的功能。这项研究的目的是测试ARF6通路是否可能参与皮质层形成过程中的神经元迁移。我们发现,I型磷脂酰肌醇4-磷酸5-激酶r(PIP5KIr)是一种磷脂酰肌醇4,5-二磷酸(PtdIns(4,5)P2)合成酶,其功能是Arf6的下游效应因子,可能是通过将黏附成分募集到质膜来实现神经元迁移的。
英文摘要
ADP ribosylation factor is a small GTPase that regulate membrane traffic and actin remodeling through the activation of lipid modifying enzymes and recruitment of various interacting proteins such as FIP3/4 and JIP3/4. Recent evidence indicates the functional importance of ARF6 pathways in cell motility such as cancer invasion and metastasis. The aim of this study is to test the possibility whether the ARF6 pathway may be involved in neuronal migration during cortical layer formation. We found that type I phosphatidylinositol 4-phosphate 5-kinase r (PIP5KIr), a phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2)-synthesizing enzyme that functions as a downstream effector of Arf6, is required for neuronal migration possibly through recruitment of adhesion components to the plasma membrane.
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DOI: --
发表时间: 2011
期刊: International Orthopaedics
影响因子: 2.7
作者: [Takaso M, Nakazawa T, Imura T, Fukushima K, Ueno M, Saito W, Shintani R, Sakagami H, et al.]
通讯作者: et al.
Type I phosphatidylinositol 4-phosphate 5-kinase r is required for neuronal migration in the mouse developing cerebral cortex
I 型磷脂酰肌醇 4-磷酸 5-激酶 r 是小鼠大脑皮层发育中神经元迁移所必需的
DOI: --
发表时间: 2013
期刊: Eur. J. Neurosci
影响因子: --
作者: [Hara Y, Fukaya M, Tamaki H, Sakagami H]
通讯作者: Sakagami H
EFA6 activates Arf6 and participates in its targeting to the Flemming body during cytokinesis
EFA6 激活 Arf6 并参与其在胞质分裂期间靶向弗莱明体
DOI: --
发表时间: 2013
期刊: FEBS Lett.
影响因子: --
作者: [Ueda, T., Hanai, A, Takei, T., Kubo, K., Ohgi, M., Sakagami, H., Takahashi, S., Shin, H.-W., and Nakayama, K.]
通讯作者: K.
成体マウス脳におけるARF6活性化因子BRAG2/IQSEC1 の細胞内局在解析
成年小鼠脑中 ARF6 激活剂 BRAG2/IQSEC1 的亚细胞定位分析
DOI: --
发表时间: 2012
期刊:
影响因子: --
作者: [深谷昌弘, 原芳伸, 阪上洋行]
通讯作者: 阪上洋行
共 37 条
    Functional involvement of the Arf6 pathway in FMPR-mediated synaptic plasticity
    • 批准号:
      25640025
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.5万
    • 财政年份:
      2013
    • 负责人:
      SAKAGAMI Hiroyuki
    • 依托单位:
    Functional analysis of the BRAG3-Arf6 pathway in the inhibitory synapse
    • 批准号:
      22300114
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $11.32万
    • 财政年份:
      2010
    • 负责人:
      SAKAGAMI Hiroyuki
    • 依托单位:
    Mechanisms for the dendritic formation by ADP ribosylation factor 6 and its functional significance in higher brain functions
    • 批准号:
      19300119
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $12.15万
    • 财政年份:
      2007
    • 负责人:
      SAKAGAMI Hiroyuki
    • 依托单位:
    Targeting mechanisms for calmodulin-dependent protein kinases and their neuronal functions
    • 批准号:
      17500219
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.24万
    • 财政年份:
      2005
    • 负责人:
      SAKAGAMI Hiroyuki
    • 依托单位:
    海外基金