Roles of phosphorylation of ERM proteins and ERM-binding membrane proteins in cellular morphogenesis
Roles of phosphorylation of ERM proteins and ERM-binding membrane proteins in cellular morphogenesis
批准号:
11670117
负责人:
YONEMURA Shigenobu
金额:
$2.43万
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:
1999
资助国家:
日本
项目状态:
已结题
起止时间:
1999 至 2000
中文摘要
一曰:ERM-binding membrane proteins过度表达的影响(CD 43、CD 44和ICAM-2)对微绒毛形成的影响这些膜蛋白在L和CV 1细胞中的过表达导致微绒毛的延长,表明这些蛋白与ERM蛋白一起是微绒毛的主要成分。2:在COOH末端苏氨酸残基磷酸化的ERM蛋白(CPERMs)的定位我们开发了新的固定方案,使用三氯乙酸作为固定剂,以确定精确定位的CPERMs。3:ERM蛋白在细胞形态发生中的活化使用Rho抑制剂C3、蛋白激酶抑制剂staurosporine和PIP 2抑制剂新霉素揭示了Rho活性和ERM蛋白磷酸化的重要性取决于细胞类型。然而,发现PIP 2对于ERM蛋白的活化以及微绒毛的形成无一例外地是必需的。
英文摘要
1 : Effects of overexpression of ERM-binding membrane proteins (CD43, CD44 and ICAM-2) on microvilli formationOverexpression of these membrane proteins in L and CV1 cells resulted in elongation of microvilli, indicating these proteins are major components of microvilli together with ERM proteins.2 : Localization of ERM proteins phosphorylated at the COOH-terminal threonine residue (CPERMs)We developed new fixation protocol using trichloroacetic acid as a fixative to determine precise localization of CPERMs. They were localized just beneath the plasma membrane of microvilli, reflecting that CPERMs are activated ERM proteins as membrane-cytoskeleton cross-linkers.3 : ERM protein activation in cellular morphogenesisUse of Rho inhibitor, C3, protein kinase inhibitor, staurosporine, and PIP2 inhibitor, neomycin revealed that importance of Rho activity and phosphorylation of ERM proteins depends on cell type. However PIP2 was found to be essential without exception for activation of ERM proteins as well as microvilli formation.
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月田承一郎 他、: "岩波講座・現代医学の基礎 分子・細胞の生物学II 第6章 細胞骨格と細胞運動"岩波書店. 17 (2000)
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Yoshinori Doi: "Normal development of mice and unimpaired cell adhesion/cell Motility/Actin-based cytoskeleton without compasatory・・・"J.Biological Chemistry. 274. 2315-2321 (1999)
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Noriyuki Sonoda: "Clostridium perfrongens enterotoxin fragment removes specific claudins from tight junction strands : Evidence for direct involvement・・・"J.Cell Biology. 147. 195-204 (1999)
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S.Yonemura, Sa.Tsukita and Sh.Tsukita: "Direct involvement of ezrin/radixin/moesin (ERM) -binding membrane proteins in the organization of microvilli in collaboration with activated ERM proteins."J.Cell Biol.. 145. 1497-1509 (1999)
S.Yonemura、Sa.Tsukita 和 Sh.Tsukita:“ezrin/radixin/moesin (ERM) 结合膜蛋白与激活的 ERM 蛋白协同参与微绒毛组织的直接参与。”J.Cell Biol.. 145. 1497
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N.Sonoda, M.Furuse, H.Sasaki, S.Yonemura, J.Katahira, Y.Horiguchi and Sh.Tsukita: "Clostridium perfringens enterotoxin fragment removes specific claudins from tight strands : evidence for direct involvement of claudins in tight junction junction barrier."
N.Sonoda、M.Furuse、H.Sasaki、S.Yonemura、J.Katahira、Y.Horiguchi 和 Sh.Tsukita:“产气荚膜梭菌肠毒素片段从紧密链中去除特定的密蛋白:密蛋白直接参与紧密连接的证据
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