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Study on activity of the signaling pathways regulating hepatocyte differentiation during rat liver regeneration

机译:大鼠肝再生过程中调控肝细胞分化的信号通路活性研究

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To understand the mechanism of hepatocyte differentiation during rat liver regeneration (LR) at the gene transcription level, Rat Genome 230 2.0 Array was used to determine the gene expression changes of hepatocytes. Then the genes associated with cell differentiation and their signaling pathways were searched by NCBI, QIAGEN and KEGG webs, and their signaling activities were calculated by spectral function Ep(t) based on the expression profiles. The key genes associated with the signaling pathways and cell differentiation were analyzed and verified by the same kind extraction method. The mechanism of hepatocyte differentiation during rat LR was analyzed by Ingenuity Pathway Analysis 9.0 (IPA). The results showed that 42 signaling pathways regulated cell differentiation and the Ep(t) values of IL-9 signaling pathway and its JAK/STAT and PI3K/AKT branches, PEDF signaling pathway and its NF-κB and Ras/ERK branches were significantly increased in the progression phase (6–72 h after partial hepatectomy [PH]) of rat LR, and the Ep(t) values of hepatocyte differentiation were also significantly increased. ERK/MAPK signaling pathway was significantly increased in the priming (0.5–6 h after PH) and progression phase, and hepatocyte differentiation were also significantly increased. In conclusion, among the 42 signaling pathways that regulated cell differentiation, the signaling activity of IL-9 signaling pathway and its JAK/STAT and PI3K/AKT branches, PEDF signaling activity and its NF-κB and Ras/ERK branches, and ERK/MAPK signaling activity were significantly increased and promoted hepatocyte differentiation in rat LR. Meanwhile, the expression of MYC involved in mentioned signaling pathways and expression of AGT, BCL2, IL10, CCND1, PLAT, and NF1 related to cell differentiation were increased significantly.
机译:为了了解在基因转录水平上大鼠肝再生(LR)期间肝细胞分化的机制,使用了Rat Genome 230 2.0 Array来确定肝细胞的基因表达变化。然后通过NCBI,QIAGEN和KEGG网搜索与细胞分化相关的基因及其信号传导途径,并根据表达谱通过光谱函数Ep(t)计算其信号传导活性。用相同的提取方法分析并验证了与信号通路和细胞分化有关的关键基因。通过Ingenuity Pathway Analysis 9.0(IPA)分析了大鼠LR期间肝细胞分化的机制。结果显示42条信号通路调节细胞分化,IL-9信号通路及其JAK / STAT和PI3K / AKT分支,PEDF信号通路及其NF-κB和Ras / ERK分支的Ep(t)值显着增加在大鼠LR的进展阶段(部分肝切除[PH]后6-72小时),肝细胞分化的Ep(t)值也显着增加。 ERK / MAPK信号通路在启动阶段(PH后0.5–6 h)和进展阶段显着增加,肝细胞分化也显着增加。总之,在调控细胞分化的42条信号通路中,IL-9信号通路及其JAK / STAT和PI3K / AKT分支的信号传导活性,PEDF信号活性及其NF-κB和Ras / ERK分支以及ERK / MAPK信号活性明显增加,并促进大鼠LR肝细胞分化。同时,参与信号转导的MYC的表达以及与细胞分化有关的AGT,BCL2,IL10,CCND1,PLAT和NF1的表达均显着增加。

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