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转化生长因子α诱导胶质瘤细胞中Hes1的上调和核转位。

TGF-alpha induces upregulation and nuclear translocation of Hes1 in glioma cell.

作者信息

Zheng Yingfeng, Lin Ling, Zheng Zhihong

机构信息

Department of Biochemistry and Molecular Biology, Research Center of Molecular Medicine, Fujian Medical University, Fuzhou, PR China.

出版信息

Cell Biochem Funct. 2008 Aug;26(6):692-700. doi: 10.1002/cbf.1494.

Abstract

Both the Notch-signaling pathway and extracellular signal regulated kinase (ERK) cascade are involved in a wide variety of biological processes, such as proliferation, differentiation, survival, and tumorigenesis. Their dysregulation in recent studies have been shown to be associated with glioma formation. Here, we show that transforming growth factor-alpha (TGF-alpha) stimulated glioma cell line U251 growth and can partly compensate for the inhibitory effect of Notch-signaling inhibitor DAPT. The effect of TGF-alpha on ERK1/2 phosphorylation was prompt and transient and could be inhibited by mitogen-activated/extracellular signal-regulated kinase kinase 1/2 (MEK1/2) specific inhibitor PD98059. Moreover, TGF-alpha was capable of up-regulating Hairy-enhancer of split1 (Hes1) expression which was independent of Notch1 activation, and of introducing Hes1 nuclear import in the presence of ERK1/2 activation. Collectively, our data suggest a potential linkage between ERK activation and the Notch-signaling pathway.

摘要

Notch信号通路和细胞外信号调节激酶(ERK)级联均参与多种生物学过程,如增殖、分化、存活和肿瘤发生。近期研究表明,它们的失调与胶质瘤形成有关。在此,我们发现转化生长因子-α(TGF-α)可刺激胶质瘤细胞系U251生长,并能部分补偿Notch信号抑制剂DAPT的抑制作用。TGF-α对ERK1/2磷酸化的作用迅速且短暂,可被丝裂原活化/细胞外信号调节激酶激酶1/2(MEK1/2)特异性抑制剂PD98059抑制。此外,TGF-α能够上调分裂增强子毛状蛋白1(Hes1)的表达,该表达独立于Notch1激活,并且在ERK1/2激活的情况下可促使Hes1核输入。总体而言,我们的数据表明ERK激活与Notch信号通路之间存在潜在联系。

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