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首页> 外文期刊>Journal of Korean medical science. >Microarray Analysis of Thyroid Stimulating Hormone, Insulin-Like Growth Factor-1, and Insulin-Induced Gene Expression in FRTL-5 Thyroid Cells
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Microarray Analysis of Thyroid Stimulating Hormone, Insulin-Like Growth Factor-1, and Insulin-Induced Gene Expression in FRTL-5 Thyroid Cells

机译:FRTL-5甲状腺细胞中甲状腺刺激激素,胰岛素样生长因子-1和胰岛素诱导的基因表达的微阵列分析。

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To determine which genes are regulated by thyroid stimulating hormone (thyrotropin, TSH), insulin and insulin-like growth factor-1 (IGF-1) in the rat thyroid, we used the microarray technology and observed the changes in gene expression. The expressions of genes for bone morphogenetic protein 6, the glucagon receptor, and cyclin D1 were increased by both TSH and IGF-1; for cytochrome P450, 2c37, the expression was decreased by both. Genes for cholecystokinin, glucuronidase, beta, demethyl-Q 7, and cytochrome c oxidase, subunit VIIIa, were up-regulated; the genes for ribosomal protein L37 and ribosomal protein L4 were down-regulated by TSH and insulin. However, there was no gene observed to be regulated by all three: TSH, IGF-1, and insulin molecules studied. These findings suggest that TSH, IGF-1, and insulin stimulate different signal pathways, which can interact with one another to regulate the proliferation of thyrocytes, and thereby provide additional influence on the process of cellular proliferation.
机译:为了确定甲状腺中的甲状腺刺激激素(促甲状腺激素,TSH),胰岛素和胰岛素样生长因子-1(IGF-1)调控哪些基因,我们使用了微阵列技术并观察了基因表达的变化。 TSH和IGF-1均可增加骨形态发生蛋白6,胰高血糖素受体和细胞周期蛋白D1的基因表达。对于细胞色素P450、2c37,两者的表达均降低。胆囊收缩素,葡糖醛酸糖苷酶,β,去甲基-Q 7和细胞色素c氧化酶VIIIa亚基的基因上调; TSH和胰岛素下调了核糖体蛋白L37和L4的基因。但是,没有观察到受以下三种基因调控的基因:TSH,IGF-1和研究的胰岛素分子。这些发现表明,TSH,IGF-1和胰岛素刺激不同的信号通路,这些信号通路可以相互影响以调节甲状腺细胞的增殖,从而对细胞增殖的过程提供额外的影响。

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