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NFkappaB-p65 dependent transcriptional regulation of glycosyltransferases in human colon adenocarcinoma HT-29 by stimulation with tumor necrosis factor alpha.

机译:通过用肿瘤坏死因子α刺激,在人结肠腺癌HT-29中NFkappaB-p65的糖基转移酶依赖转录调节。

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摘要

Regulation of fucosyltransferases (FUTs) and sialyltransferases (STs) in a human colon adenocarcinoma cell line HT-29 and nuclear factor kappaB (NFkappaB)-p65 knockdown HT-29 cells was investigated after stimulation with tumor necrosis factor alpha (TNFalpha) using real time PCR. TNFalpha stimulation induced the biphasic increases in expression of NFkappaB-p65, ST3Gal I, FUT IV, ST3Gal IV and ST6GalNAc III mRNAs and the transient increase in expression of ST6Gal I mRNA and the decrease in ST3GalNAc IV mRNA. In NFkappaB-p65 knockdown HT-29 cells, the biphasic and transient increases in all of these mRNA expression induced with TNFalpha were diminished. On the other hand, NFkappaB-p65 siRNA enhanced the constitutive expression levels of ST3GalNAc IV mRNA which was suppressed by TNFalpha. Transcription activities of ST3Gal I reporter gene from nt -1050 5'-flanking region to translation initiation site which has consensus NFkappaB binding sites were up-regulated by stimulation with TNFalpha in HT-29 cells.The promoter activities for deletion constructs of each NFkappaB binding sites were determined using dual luciferase assay. The results indicated that constitutive promoter activities were detected at nt -120 5'-flanking translation initiation site and TNFalpha enhanced ST3Gal I gene expression through NFkappaB binding sites in HT-29 cells. Combination of stimulation with TNFalpha and NFkappaB knockdown with siRNA is useful for determination of NFkappaB dependent transcriptional regulation.
机译:使用实时肿瘤坏死因子α(TNFalpha)刺激后,研究了人类结肠腺癌细胞HT-29和核因子κB(NFkappaB)-p65敲低HT-29细胞中岩藻糖基转移酶(FUTs)和唾液酸转移酶(STs)的调控。 PCR。 TNFalpha刺激诱导NFkappaB-p65,ST3Gal I,FUT IV,ST3Gal IV和ST6GalNAc III mRNA的双相表达,以及ST6Gal I mRNA的瞬时表达增加和ST3GalNAc IV mRNA的减少。在NFkappaB-p65基因敲除的HT-29细胞中,由TNFα诱导的所有这些mRNA表达的双相和瞬时增加都减少了。另一方面,NFkappaB-p65 siRNA增强了ST3GalNAc IV mRNA的组成型表达水平,该水平被TNFalpha抑制。通过在HT-29细胞中用TNFα刺激,ST3Gal I报告基因从nt -1050 5'侧翼区到具有共有NFkappaB结合位点的翻译起始位点的转录活性被上调。每种NFkappaB结合的缺失构建体的启动子活性使用双重荧光素酶测定法确定位点。结果表明在nt -120 5'侧翼翻译起始位点检测到组成型启动子活性,并且TNFα通过HT-29细胞中的NFκB结合位点增强了ST3Gal I基因表达。 TNFα刺激与siRNA结合的NFkappaB组合刺激可用于确定NFkappaB依赖的转录调控。

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