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转录因子egr-1参与佛波酯12-肉豆蔻酸酯13-乙酸酯诱导的K562细胞巨核细胞分化。

Transcription factor egr-1 is involved in phorbol 12-myristate 13-acetate-induced megakaryocytic differentiation of K562 cells.

作者信息

Cheng T, Wang Y, Dai W

机构信息

Hipple Cancer Research Center, Dayton, Ohio 45439-2092.

出版信息

J Biol Chem. 1994 Dec 9;269(49):30848-53.

PMID:7983016
Abstract

Transcription factors play important roles in regulating cell growth and differentiation. egr-1, a transcription factor of the zinc finger family, is rapidly activated in many types of cells after mitogen treatment. In this report, we demonstrate that egr-1 mRNA expression, detected by Northern blotting, is activated within 30 min of treatment of the erythroleukemia cell line K562 with phorbol 12-myristate 13-acetate (PMA), and the increased egr-1 mRNA level is associated with an elevated egr-1 antigen expression detected by Western blotting and with its DNA binding activity shown by the gel mobility shift assay. In addition, PMA-mediated activation of egr-1 mRNA expression involves no new protein synthesis and is followed by sequential down-regulation of the mRNA level of GATA-1 and glycophorin A. On the other hand, CD41a surface antigen expression is dramatically up-regulated. Furthermore, enforced expression of egr-1, through transfection of K562 cells with the egr-1 expression plasmid construct, results in expression of the egr-1 transcript that accompanies a significant accumulation on the cell surface of CD41a but not CD14 nor glycophorin A. These observations suggest that egr-1 is involved in regulating PMA-induced megakaryocytic differentiation of K562 cell line.

摘要

转录因子在调节细胞生长和分化中发挥着重要作用。egr-1是锌指家族的一种转录因子,在有丝分裂原处理后,它能在多种类型的细胞中迅速被激活。在本报告中,我们证明,通过Northern印迹法检测到,用佛波酯12-肉豆蔻酸酯13-乙酸酯(PMA)处理红白血病细胞系K562后30分钟内,egr-1 mRNA表达被激活,并且通过Western印迹法检测到的egr-1抗原表达升高以及凝胶迁移率变动分析显示的其DNA结合活性增强与egr-1 mRNA水平增加相关。此外,PMA介导的egr-1 mRNA表达激活不涉及新的蛋白质合成,随后GATA-1和血型糖蛋白A的mRNA水平会依次下调。另一方面,CD41a表面抗原表达显著上调。此外,通过用egr-1表达质粒构建体转染K562细胞来强制表达egr-1会导致egr-1转录本的表达,同时伴随着CD41a在细胞表面的显著积累,但CD14和血型糖蛋白A则没有。这些观察结果表明,egr-1参与调节PMA诱导的K562细胞系巨核细胞分化。

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