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原癌基因c-fos与脱水过程中血管加压素基因表达的调控

Proto-oncogene c-fos and the regulation of vasopressin gene expression during dehydration.

作者信息

Ding J M, Carver W C, Terracio L, Buggy J

机构信息

Department of Physiology, School of Medicine, University of South Carolina, Columbia 29208.

出版信息

Brain Res Mol Brain Res. 1994 Feb;21(3-4):247-55. doi: 10.1016/0169-328x(94)90255-0.

DOI:10.1016/0169-328x(94)90255-0
PMID:8170349
Abstract

Secretion of the antidiuretic hormone (ADH) vasopressin is increased when body fluid homeostasis is disturbed by dehydration. Associated with this increased secretion is an elevation of vasopressin mRNA in magnocellular hypothalamic neurons projecting to the posterior pituitary. The proto-oncogene c-fos codes for a nuclear phospho-protein Fos which binds to specific DNA elements and acts as a transcriptional regulator coupling short-term extracellular stimuli to long-term responses by altering secondary target gene expression. This study in rats examined the time courses of dehydration induced c-fos expression and the change of vasopressin gene expression in the magnocellular neurons of the hypothalamus. Immunocytochemical and in situ hybridization study demonstrated that c-fos was induced by acute intracellular dehydration in the hypothalamic magnocellular nuclei of paraventricular (PVN), supraoptic (SON), and accessory groups such as nucleus circularis. Double-label immunocytochemical study co-localized Fos and vasopressin-neurophysin immunoreactivity in the same magnocellular neurons in the SON and PVN. In situ hybridization analysis after acute dehydration revealed a rapid and transient c-fos induction followed by a persistent increase in vasopressin mRNA for up to 2 days even after rehydration. Furthermore, prevention of c-fos translation by pretreatment with protein synthesis inhibitor cycloheximide attenuated this dehydration induced increase in vasopressin mRNA. This study demonstrated that an increase in vasopressin transcription after acute dehydration is dependent on an early phase of protein synthesis.

摘要

当脱水扰乱体液平衡时,抗利尿激素(ADH)血管加压素的分泌会增加。与此分泌增加相关的是,投射到垂体后叶的下丘脑大细胞神经元中血管加压素mRNA水平升高。原癌基因c-fos编码一种核磷蛋白Fos,它与特定的DNA元件结合,并作为转录调节因子,通过改变次级靶基因的表达,将短期细胞外刺激与长期反应偶联起来。本项针对大鼠的研究考察了脱水诱导的c-fos表达的时间进程以及下丘脑中大细胞神经元中血管加压素基因表达的变化。免疫细胞化学和原位杂交研究表明,急性细胞内脱水可诱导室旁核(PVN)、视上核(SON)以及环状核等附属核团的下丘脑大细胞中c-fos的表达。双标记免疫细胞化学研究在SON和PVN的同一大细胞神经元中共同定位了Fos和血管加压素-神经垂体素免疫反应性。急性脱水后的原位杂交分析显示,c-fos诱导迅速且短暂,随后即使在补液后,血管加压素mRNA仍持续增加长达2天。此外,用蛋白质合成抑制剂环己酰亚胺预处理以阻止c-fos翻译,可减弱这种脱水诱导的血管加压素mRNA增加。本研究表明,急性脱水后血管加压素转录的增加依赖于蛋白质合成的早期阶段。

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