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胰岛素样生长因子-I(IGF-I)受体基因在大鼠脑和肝脏发育过程中以及成年大鼠肝脏再生过程中的表达。

Expression of insulin-like growth factor-I (IGF-I) receptor gene in rat brain and liver during development and in regenerating adult rat liver.

作者信息

Santos A, Yusta B, Fernández-Moreno M D, Blázquez E

机构信息

Department of Biochemistry and Molecular Biology, Faculty of Medicine, Complutense University, Madrid, Spain.

出版信息

Mol Cell Endocrinol. 1994 May;101(1-2):85-93. doi: 10.1016/0303-7207(94)90222-4.

DOI:10.1016/0303-7207(94)90222-4
PMID:9397940
Abstract

Insulin-like growth factor-I (IGF-I) is involved in the growth and development of liver and brain during fetal life by acting through specific plasma membrane receptors. In an attempt to determine how the changes in IGF-I receptor number are regulated during development, we have compared [125I]IGF-I binding to membrane fractions with the concentration of IGF-I receptor mRNA in rat liver and brain. IGF-I binding to liver membranes was 4.5 times higher in 20-day-old fetuses than in adult rats. After partial hepatectomy (70%) in adult rats a transient 2-fold increase of IGF-I binding to liver membranes was observed. In fetal and regenerating liver increases similar to those observed for IGF-I binding were observed in IGF-I receptor mRNA concentrations. In brain microsomes IGF-I binding was 3.5 times higher in 20-day-old fetuses than in adults. This difference reflects a similar change in the number of IGF-I receptors without modifications in the affinity of the receptor for the ligand. In contrast to the liver, no significant changes in the concentration of IGF-I receptor mRNA were observed in the developing brain when determined by hybridization solution, Northern blot or RNase protection analysis. These findings suggest that in the liver, the IGF-I receptor gene is regulated at pretranslational level during development and regeneration, while in brain it is preferentially regulated at translational or posttranslational level.

摘要

胰岛素样生长因子-I(IGF-I)在胎儿期通过特定的质膜受体发挥作用,参与肝脏和大脑的生长发育。为了确定在发育过程中IGF-I受体数量的变化是如何被调节的,我们比较了大鼠肝脏和大脑中[125I]IGF-I与膜组分的结合情况以及IGF-I受体mRNA的浓度。20日龄胎儿肝脏膜上的IGF-I结合量比成年大鼠高4.5倍。成年大鼠部分肝切除(70%)后,观察到肝脏膜上IGF-I结合量短暂增加2倍。在胎儿肝脏和再生肝脏中,IGF-I受体mRNA浓度的增加与IGF-I结合量的增加相似。在脑微粒体中,20日龄胎儿的IGF-I结合量比成年大鼠高3.5倍。这种差异反映了IGF-I受体数量的类似变化,而受体对配体的亲和力没有改变。与肝脏不同,通过杂交液、Northern印迹或核糖核酸酶保护分析测定时,发育中的大脑中IGF-I受体mRNA浓度没有显著变化。这些发现表明,在肝脏中,IGF-I受体基因在发育和再生过程中在转录前水平受到调节,而在大脑中,它优先在翻译或翻译后水平受到调节。

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