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在12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯诱导的HL - 60细胞分化过程中,吡咯烷二硫代氨基甲酸盐对波形蛋白基因表达的转录抑制作用

Transcriptional repression of vimentin gene expression by pyrroline dithiocarbamate during 12-O-tetradecanoylphorbol-13-acetate-dependent differentiation of HL-60 cells.

作者信息

Zheng Meizi, Son Mee-Young, Park Chung, Park Jong-Il, Jo Eun-Kyeong, Yoon Wan-Hee, Park Seung-Kiel, Hwang Byung-Doo, Lim Kyu

机构信息

Department of Biochemistry, College of Medicine, Chungnam National University, Daejeon 301-747, Korea.

出版信息

Oncol Rep. 2005 Sep;14(3):713-7.

Abstract

Vimentin is a member of the intermediate filament family, and the NF-kappaB binding site is located in the human vimentin promoter. To gain insight into the role of NF-kappaB in the regulation of the vimentin gene during 12-O-tetradecanoylphorbol-13-acetate (TPA)-dependent differentiation of HL-60 cells, the effect of pyrrolidine dithiocarbamete (PDTC) has been investigated using Northern blot hybridization and DNA mobility shift assay. PDTC inhibited macrophage-like morphologic change of HL-60 cells by TPA. TPA-dependent increase of vimentin mRNA level was decreased in a time- and dose-dependent manner by pretreatment with PDTC. One DNA-protein complex was formed by DNA mobility shift assay when the NF-kappaB or AP-1 binding sites were incubated with nuclear extract prepared from TPA-treated HL-60 cells, but no protein bound in control HL-60 cells without TPA. After PDTC pretreatment, NF-kappaB binding activity vanished but AP-1 binding activity was unchanged. Taken together, these results suggest that NF-kappaB may be an essential transacting factor for transcriptional repression of the vimentin gene by PDTC during TPA-dependent differentiation of HL-60 cells.

摘要

波形蛋白是中间丝蛋白家族的一员,核因子-κB(NF-κB)结合位点位于人类波形蛋白启动子中。为深入了解在12-十四酰佛波醇-13-乙酸酯(TPA)诱导的HL-60细胞分化过程中NF-κB在波形蛋白基因调控中的作用,运用Northern印迹杂交和DNA迁移率变动分析研究了吡咯烷二硫代氨基甲酸盐(PDTC)的作用。PDTC抑制了TPA诱导的HL-60细胞向巨噬细胞样形态的转变。用PDTC预处理后,TPA诱导的波形蛋白mRNA水平升高呈时间和剂量依赖性降低。当NF-κB或AP-1结合位点与从TPA处理的HL-60细胞制备的核提取物孵育时,通过DNA迁移率变动分析形成了一种DNA-蛋白质复合物,但在未用TPA处理的对照HL-60细胞中无蛋白质结合。PDTC预处理后,NF-κB结合活性消失,但AP-1结合活性未改变。综上所述,这些结果表明在TPA诱导的HL-60细胞分化过程中,NF-κB可能是PDTC对波形蛋白基因转录抑制作用所必需的反式作用因子。

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