Functions and mode of action of novel regulatory systems for cell adhesion and motility
Functions and mode of action of novel regulatory systems for cell adhesion and motility
批准号:
12680636
负责人:
NAKANISHI Hiroyuki
金额:
$2.37万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2000
资助国家:
日本
项目状态:
已结题
起止时间:
2000 至 2001
中文摘要
我们发现了一种新的细胞粘附调控系统。该系统由连接素和脱落素组成。连接蛋白是一种类似免疫球蛋白的细胞粘附分子,而afadin是一种连接连接蛋白和肌动蛋白细胞骨架的f -aotin结合蛋白。连接素-黄素系统在上皮细胞中组织粘附物和紧密连接。我们还发现了一种新的细胞运动调节系统。该系统由frabin和Cdc42小G蛋白组成。Frabin是一种激活Cdc42的f -actin混合蛋白。在2000- 2001年的支持下,我们研究了这些连接素-afadin和frabin-Cdc42系统的功能和作用方式。结果表明:(1)在上皮细胞中,连接素-afadin系统将cadherin-catenin和jam - zo - 1系统招募到连接素为基础的细胞-细胞粘附位点。在神经元中,连接素-腺嘌呤系统定位于突触,参与突触的信息传递。在睾丸中,连接素-卵黄素系统参与支持细胞-精子细胞连接的形成,对精子细胞的形态发生至关重要。(2) Frabin与特定的肌动蛋白和膜结构结合,激活这些结构附近的Cdc42和Rac小G蛋白,最终导致细胞运动。frabin的f -actin结合活性与cdc42激活活性协同作用于细胞运动。
英文摘要
We have found a novel regulatory system for cell adhesion. This system consists of nectin and afadin. Nectin is an immunoglobulin-like cell adhesion molecule, and afadin is an F-aotin-binding protein that connects nectin to the actin cytoskeleton.The nectin-afadin system organizes adherens and tight jjunctions in epithelial cells.We have also found a novel regulatory system for cell motility. This system consists of frabin and Cdc42 small G protein. Frabin is an F-actin-blnding protein that activates Cdc42. During this support from2000-to 2001, we have studied the functions and mode of action of these nectin-afadin and frabin-Cdc42 systems. The results obtained are as follows :(1) In epithelial cells, the nectin-afadin system recruits the cadherin-catenin and JAM-ZO-lsystems to nectin-based cell-cell adhesion sites. In neurons, the nectin-afadinsystemis localized at synapses and involved information of synapses. In testis, the nectin-afadin system is involved in formation of Sertoli-spermatid junctions and essential for spermatid morphogenesis.(2) Frabin associates with specific actin and membrane structures and activates not only Cdc42 and but also Rac small G protein in the vicinity of these structures, eventually to leading to cell motility. The F-actin-binding activity of frabin cooperatively functions with the Cdc42-activating activity in cell motility.
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Ikeda, W.: "Identification of splicing variants of frabin with partly I different functions and tissue distribution"Biochem. Biophys. Res. Commun. 286-5. 1066-1072 (2001)
Ikeda, W.:“具有部分不同功能和组织分布的 frabin 剪接变体的鉴定”Biochem。
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Ikeda, W.: "Identification of splicing variants of frabin with partly different functions and tissue distribution"Biochem.Biophys.Res.Commun.. 286・5. 1066-1072 (2001)
池田W.:“具有部分不同功能和组织分布的frabin剪接变体的鉴定”Biochem.Biophys.Res.Commun. 286・5(2001)。
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Kim, Y.: "Association of frabin with specific actin and membrane structures"Genes Cells. (in press). (2002)
Kim, Y.:“frabin 与特定肌动蛋白和膜结构的关联”Genes Cells。
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Sakisaka,T.: "Requirement of interaction of Nectin-1α/HveC with afadin for efficient cell-cell spread of herpes simplex virus type 1."J.Virol.. (in press). (2001)
Sakisaka, T.:“1 型单纯疱疹病毒有效细胞间传播需要 Nectin-1α/HveC 与 afadin 相互作用。”J.Virol..(出版中)。
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Nishioka, H.: "Localization of 1-afadin at puncta adhaerentia-like junctions between the mossy fiber terminals and the dendritici trunks of pyramidal cells in the adult mouse hippocampus"J. Comp. Neurol.. 424・2. 297-306 (2000)
Nishioka, H.:“1-afadin 在成年小鼠海马苔藓纤维末端和锥体细胞树突状连接处的定位”J.Neurol.. 297-306。 2000)
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共 26 条
Interactions of transportsome and cytoskeleton
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批准号:17081014
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项目类别:Grant-in-Aid for Scientific Research on Priority Areas
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资助金额:$38.72万
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财政年份:2005
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负责人:NAKANISHI Hiroyuki
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依托单位:
Mechanisms of formation of cell-cell junctions
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批准号:15390099
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$8.58万
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财政年份:2003
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负责人:NAKANISHI Hiroyuki
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依托单位:
海外基金