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一种对无翅信号有反应的新型果蝇施奈德S2细胞系的鉴定与特性分析。

Identification and characterization of a novel line of Drosophila Schneider S2 cells that respond to wingless signaling.

作者信息

Yanagawa S, Lee J S, Ishimoto A

机构信息

Department of Viral Oncology, Institute for Virus Research, Kyoto University, Kyoto 606-8507, Japan.

出版信息

J Biol Chem. 1998 Nov 27;273(48):32353-9. doi: 10.1074/jbc.273.48.32353.

Abstract

Wingless (Wg) treatment of Drosophila wing disc clone 8 cells leads to Armadillo (Arm) protein elevation, and this effect has been used as the basis of in vitro assays for Wg protein. Previously analyzed stocks of Drosophila Schneider S2 cells could not respond to added Wg, because they lack the Wg receptor, Dfrizzled-2. However, we found that a line of S2 cells obtained from another source express Dfrizzled-2 and Dfrizzled-1. Thus, we designated this cell line as S2R+ (S2 receptor plus). S2R+ cells respond to addition of extracellular Wg by elevating Arm and DE-cadherin protein levels and by hyperphosphorylating Dsh, just as clone 8 cells do. Moreover, overexpression of Wg in S2R+, but not in S2 cells, induced the same changes in Dsh, Arm, and DE-cadherin proteins as induced in clone 8 cells, indicating that these events are common effects of Wg signaling, which occurs in cells expressing functional Wg receptors. In addition, unphosphorylated Dsh protein in S2 cells was phosphorylated as a consequence of expression of Dfrizzled-2 or mouse Frizzled-6, suggesting that basal structures common to various frizzled family proteins trigger this phosphorylation of Dsh. S2R+ cells are as sensitive to Wg as are clone 8 cells but can grow in simpler medium. Therefore, the S2R+ cell line is likely to prove highly useful for in vitro analyses of Wg signaling.

摘要

对果蝇翅盘克隆8细胞进行无翅(Wg)处理会导致犰狳(Arm)蛋白水平升高,这种效应已被用作Wg蛋白体外检测的基础。先前分析的果蝇施奈德S2细胞株对添加的Wg无反应,因为它们缺乏Wg受体Dfrizzled-2。然而,我们发现从另一个来源获得的一株S2细胞表达Dfrizzled-2和Dfrizzled-1。因此,我们将该细胞株命名为S2R+(S2受体阳性)。S2R+细胞通过提高Arm和DE-钙黏蛋白水平以及使Dsh过度磷酸化来响应细胞外Wg的添加,就像克隆8细胞一样。此外,在S2R+细胞中而非S2细胞中过表达Wg,会诱导Dsh、Arm和DE-钙黏蛋白蛋白发生与克隆8细胞中相同的变化,这表明这些事件是Wg信号传导的常见效应,发生在表达功能性Wg受体的细胞中。此外,S2细胞中未磷酸化的Dsh蛋白由于Dfrizzled-2或小鼠Frizzled-6的表达而被磷酸化,这表明各种卷曲蛋白家族蛋白共有的基础结构会触发Dsh的这种磷酸化。S2R+细胞对Wg的敏感性与克隆8细胞相同,但能在更简单的培养基中生长。因此,S2R+细胞株可能对Wg信号传导的体外分析非常有用。

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