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丁酸诱导的F-98胶质瘤细胞分化中c-fos表达的分析

Analysis of c-fos expression in the butyrate-induced F-98 glioma cell differentiation.

作者信息

Tang S J, Huang Y M, Wang F F

机构信息

Institute of Marine Biotechnology, National Ocean University, Keelong, Taiwan.

出版信息

Biochem J. 1995 Feb 15;306 ( Pt 1)(Pt 1):47-56. doi: 10.1042/bj3060047.

Abstract

The functional induction of c-fos in the sodium butyrate-induced differentiation of F-98 glioma cells was studied. Fos protein level was increased by butyrate. In contrast, c-Jun protein was constitutively expressed and was not affected by butyrate. Gel-retardation assay indicates Fos as a component of the complex formed between the consensus oligonucleotide of the TPA (PMA, phorbol 12-myristate 13-acetate) response element (TRE) and nuclear extract prepared from butyrate-treated cells. Transfection studies showed that butyrate increased transcription from a multimeric TRE-driven reporter construct, and the effect was mimicked by transfecting cells with fos-expression plasmid. Furthermore, under conditions of c-fos over-expression, transactivation by butyrate was essentially abolished. These data suggest that Fos induction had a functional role in gene activation. Characterization of stable c-fos transfectants demonstrated that these cells displayed alterations in morphology, showed serum-dependent growth, had slower growth rates and grew to lower saturation densities than did untransfected F-98 cells or transfected cells that did not express c-fos. Immunofluorescent staining indicated that fos transfectants also had elevated glial fibrillary acidic protein ('GFAP') expression. Transfection of the c-fos promoter-chloramphenicol acetyltransferase fusion gene into F-98 cells revealed that activation of c-fos by butyrate was exerted at the promoter level, and sequences located within nucleotides -757 to -402 of the c-fos promoter were responsible for butyrate induction. Our data indicate that transcriptional activation of c-fos through its promoter by butyrate resulted in increased Fos protein expression. Transfection studies show that both c-fos and butyrate activate TRE-containing genes, and fos may be a downstream mediator of butyrate. Furthermore, expression of c-fos plays a major role in modulating the growth properties of F-98 cells.

摘要

研究了丁酸钠诱导F-98胶质瘤细胞分化过程中c-fos的功能诱导情况。丁酸钠可使Fos蛋白水平升高。相比之下,c-Jun蛋白呈组成性表达,不受丁酸钠影响。凝胶阻滞试验表明,Fos是TPA(佛波酯,十四酰佛波醇乙酯)反应元件(TRE)的共有寡核苷酸与丁酸钠处理细胞制备的核提取物之间形成的复合物的一个组成成分。转染研究表明,丁酸钠可增加多聚体TRE驱动的报告基因构建体的转录,用fos表达质粒转染细胞可模拟该效应。此外,在c-fos过表达的条件下,丁酸钠的反式激活作用基本被消除。这些数据表明,Fos诱导在基因激活中具有功能性作用。稳定的c-fos转染子的特性表明,这些细胞在形态上发生了改变,表现出血清依赖性生长,生长速率较慢,与未转染的F-98细胞或不表达c-fos的转染细胞相比,达到的饱和密度较低。免疫荧光染色表明,fos转染子的胶质纤维酸性蛋白(“GFAP”)表达也有所升高。将c-fos启动子-氯霉素乙酰转移酶融合基因转染到F-98细胞中发现,丁酸钠对c-fos的激活作用发生在启动子水平,c-fos启动子核苷酸-757至-402内的序列负责丁酸钠诱导。我们的数据表明,丁酸钠通过其启动子对c-fos的转录激活导致Fos蛋白表达增加。转染研究表明,c-fos和丁酸钠均可激活含TRE的基因,fos可能是丁酸钠的下游介质。此外,c-fos的表达在调节F-98细胞的生长特性中起主要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e707/1136480/cfc1bd7b41ed/biochemj00069-0058-a.jpg

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