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重组人生长激素和胰岛素样生长因子I诱导PC12细胞中的PrP基因表达。

Recombinant human growth hormone and insulin-like growth factor I induce PrP gene expression in PC12 cells.

作者信息

Lasmézas C, Deslys J P, Dormont D

机构信息

Laboratoire de Neuropathologie Expérimentale et Neurovirologie, DSV/DPTE/CRSSA/CEA, Fontenay-aux-Roses, France.

出版信息

Biochem Biophys Res Commun. 1993 Nov 15;196(3):1163-9. doi: 10.1006/bbrc.1993.2373.

Abstract

Growth factors like NGF are known to increase the expression of PrP gene, a housekeeping gene which is responsible for susceptibility to transmissible spongiform encephalopathies. We evaluated in vitro the effect of recombinant human growth hormone (hGH) and one of its in vivo effectors, the insulin-like growth factor I (IGF-I), on PrP gene expression in PC12 cells. We observed a 30% increase of PrP mRNA level after 7 day treatment by hGH at 10 micrograms/ml and potentiation of NGF effect (reaching four times baseline expression as opposed to three times baseline with NGF alone). IGF-I induced a dose-dependent increase of PrP mRNA up to twice baseline at a dose of 100 ng/ml and had an additive effect with NGF at 10 ng/ml. These preliminary results indicate that growth promoting factors may play a role in the PrP gene regulation within neuron-like cells.

摘要

已知诸如神经生长因子(NGF)等生长因子会增加朊蛋白(PrP)基因的表达,PrP基因是一种管家基因,与传染性海绵状脑病的易感性有关。我们在体外评估了重组人生长激素(hGH)及其一种体内效应因子胰岛素样生长因子I(IGF-I)对PC12细胞中PrP基因表达的影响。我们观察到,用10微克/毫升的hGH处理7天后,PrP mRNA水平增加了30%,并且增强了NGF的作用(达到基线表达的四倍,而单独使用NGF时为三倍)。IGF-I在剂量为100纳克/毫升时诱导PrP mRNA呈剂量依赖性增加,最高可达基线的两倍,并且在10纳克/毫升时与NGF具有相加作用。这些初步结果表明,生长促进因子可能在类神经元细胞内的PrP基因调控中发挥作用。

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