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Synergistic Effects of Activin A and Fibroblast Growth Factor 2 in the Modulation of Insulin Expression

机译:激活素A和成纤维细胞生长因子2在胰岛素表达调控中的协同作用。

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Diabetes is the most prevalent and serious metabolic disease, and the number of diabetic patients worldwide is increasing. The reduction of insulin biosynthes is in pancreatic β-cells is closely associated with the onset and progression of diabetes, therefore, it is important to search for ways to induce insulin-producing cells in non-β-cells. In the present study, it has been reported that activin A and a basic fibroblast growth factor 2( FGF2) , can synergistical-ly increase the insulin mRNA level, in both mouse E14 striatal primary cell cultures and the hippocampal neuronal cell line HT22. Activin A and FGF2 can jointly stimulate the nuclear translocation of Smad3 and specifically activate ERK1/2. It is interesting to note that a specific inhibitor for MEK, U0126, can efficiently block the induction of an insulin promoter activity by activin A and FGF2. This indicates that activin A collaborates with FGF2, giving a signal to induce the insulin gene through selective activation of the ERK-type MAP kinase and Smad3 in mouse striatal and HT22 cells. These data suggest that activin A may act in concert with FGF2 for the development of insulin -positive neurons.
机译:糖尿病是最普遍和最严重的代谢疾病,全世界的糖尿病患者人数正在增加。胰腺β细胞中胰岛素生物合成的减少与糖尿病的发生和发展密切相关,因此,寻找诱导非β细胞中产生胰岛素的细胞的方法很重要。在本研究中,据报道,在小鼠E14纹状体原代细胞培养物和海马神经元细胞系HT22中,激活素A和碱性成纤维细胞生长因子2(FGF2)可以协同增加胰岛素mRNA的水平。激活素A和FGF2可以共同刺激Smad3的核易位,并特异性激活ERK1 / 2。有趣的是,MEK的一种特异性抑制剂U0126可以有效地阻断激活素A和FGF2对胰岛素启动子活性的诱导。这表明激活素A与FGF2协同作用,从而通过选择性激活小鼠纹状体和HT22细胞中的ERK型MAP激酶和Smad3给出了诱导胰岛素基因的信号。这些数据表明,激活素A可与FGF2协同作用以促进胰岛素阳性神经元的发育。

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