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Restraint-induced fra-2 and c-fos expression in the rat forebrain: relationship to stress duration

机译:约束诱导的大鼠前脑中fra-2和c-fos表达:与应激持续时间的关系

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摘要

The protein product of the fra-2 gene (Fra-2), a fos-family member, can compete with Fos protein for participation in AP-1 transcription factor complexes and each protein can contribute different transactivational consequences to an AP-1 complex. To date, there is limited characterization of fra-2 mRNA expression in the rat forebrain. We examined basal and restraint-induced mRNA expression (in situ hybridization) of fra-2 in the rat forebrain and compared its temporal-spatial pattern to c-fos. In contrast to the very low basal expression of c-fos, fra-2 basal expression was moderately high throughout cortex and some subcortical structures, including prominent basal expression in the hypothalamic paraventricular nucleus (PVN). Restraint-induced fra-2 expression was quantified in the prefrontal cortex (PFC), lateral septum (LS) and PVN. Maximal fra-2 gene induction in the PFC and LS was delayed (60 min) after restraint onset with respect to c-fos (15 min), whereas in the PVN, fra-2 mRNA increased within 15 min of restraint. Additionally we compared c-fos and fra-2 gene expression in rats given shorter or longer restraint durations, but equal total time from stress onset to sample collection, to determine the extent to which the kinetics of gene induction matched that of a hypothalamic-pituitary-adrenal axis hormone response. Rats given 45 min recovery after 15 min restraint showed less c-fos expression in the PVN, less fra-2 expression in the prelimbic and infralimbic PFC, and no difference in the LS compared with rats restrained for 60 min. Thus, the expression of both genes was sensitive to stressor duration, but this sensitivity varied with brain region. Differential basal and stress-induced expression patterns of the fra-2 and c-fos genes are likely to have important functional consequences for AP-1 transcription factor dependent regulation of neural plasticity.
机译:fos家族成员fra-2基因(Fra-2)的蛋白质产物可以与Fos蛋白质竞争参与AP-1转录因子复合物的参与,并且每种蛋白质都可以对AP-1复合物产生不同的反式激活作用。迄今为止,在大鼠前脑中fra-2 mRNA表达的表征有限。我们检查了大鼠前脑中fra-2的基础和约束诱导的fra-2 mRNA表达(原位杂交),并将其时空模式与c-fos进行了比较。与c-fos的基础表达非常低相反,fra-2的基础表达在整个皮质和某些皮质下结构中均较高,包括在下丘脑室旁核(PVN)中的突出的基础表达。约束诱导的fra-2表达在前额叶皮层(PFC),侧隔(LS)和PVN中进行定量。相对于c-fos(15分钟),PFC和LS的最大fra-2基因诱导延迟(60分钟)相对于c-fos抑制(15分钟),而在PVN中,fra-2 mRNA在抑制15分钟内增加。此外,我们比较了限制时间较短或更长,但从应激发作到样品采集的总时间相等的大鼠中c-fos和fra-2基因表达的差异,以确定基因诱导的动力学与下丘脑-垂体的动力学匹配程度-肾上腺轴激素反应。与约束60分钟的大鼠相比,约束15分钟后恢复45分钟的大鼠显示,PVN中的c-fos表达较少,前肢和下肢PFC中的fra-2表达较少,而LS则无差异。因此,两个基因的表达对应激持续时间敏感,但是这种敏感度随大脑区域而变化。基础和应激诱导的 fra-2 c-fos 基因的差异表达模式可能对依赖AP-1转录因子的神经可塑性调节具有重要的功能影响。

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