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Increased DNA binding activity of NF-kB STAT-3 SMAD3 and AP-1 in acutely damaged liver

机译:急性受损肝脏中NF-kBSTAT-3SMAD3和AP-1的DNA结合活性增加

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摘要

AIM: To investigate the role of genes and kinetics of specific transcription factors in liver regeneration, and to analyze the gene expression and the activity of some molecules crucially involved in hepatic regeneration.METHODS: USING gel-shift assay and RT-PCR, transcription factors, such as NF-κB, STAT-3, SMAD3 and AP-1, and gene expression of inducible nitric oxide synthase (iNOS), hepatocyte growth factor (HGF) and c-met were analyzed in an animal model of chemically induced hepatectomy.RESULTS: Gene expression of HGF and its receptor c-met peaked at 3 h and 24 h after acute CCl4 intoxi-cation. iNOS expression was only observed from 6 to 48 h. Transcriptional factor NF-κB had an early activation at 30 min after acute liver damage. STAT-3 peaked 3 h post-intoxication, while AP-1 displayed a peak of activation at 48 h. SMAD3 showed a high activity at all analyzed times.CONCLUSION: TNF-α and IL-6 play a central role in hepatic regeneration. These two molecules are responsible for triggering the cascade of events and switch-on of genes involved in cell proliferation, such as growth factors, kinases and cyclins which are direct participants of cell proliferation.
机译:目的:研究基因和特定转录因子在肝再生中的作用,并分析其基因表达和一些关键参与肝再生的分子的活性。方法:利用凝胶迁移法和RT-PCR,转录因子在化学诱导肝切除的动物模型中分析了NF-κB,STAT-3,SMAD3和AP-1等基因,以及诱导型一氧化氮合酶(iNOS),肝细胞生长因子(HGF)和c-met的基因表达。结果:急性CCl4刺激后3h和24h,HGF及其受体c-met的基因表达达到峰值。仅在6至48小时内观察到iNOS表达。急性肝损伤后30分钟,转录因子NF-κB具有早期活化。 STAT-3在中毒后3小时达到峰值,而AP-1在48小时时显示出活化峰值。结论:TNF-α和IL-6在肝细胞再生中起着重要的作用。这两个分子负责触发事件的级联和参与细胞增殖的基因的开启,这些基因例如是细胞增殖的直接参与者的生长因子,激酶和细胞周期蛋白。

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