Jun和Fos蛋白对神经系统基因转录的调控

Manfred Zimmermann, Thomas Herdegen
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引用次数: 45

摘要

躯体感觉和内脏伤害感受器的急性和慢性刺激之后,中枢神经系统中立即早期基因(IEG)编码转录因子如Jun、Fos和Krox蛋白的诱导。外周神经的横断也会导致被切开的神经元和突触相关的中枢神经元的IEG表达。免疫组织化学研究表明,神经系统IEG表达的时空模式是复杂的,并依赖于有害刺激的类型和强度。直接早期基因编码蛋白控制其他靶基因的转录,其中一些已被确定。作者假设,脑电图的激活代表了有害传入输入传递到神经元细胞程序持久改变的步骤。因此,刺激诱导的基因表达变化可能改变神经元的表型,这意味着神经元功能的病理生理改变。即时早期基因表达的意义超越了其目前在神经科学中作为神经元活动标记的用途,因为它可能为理解与慢性疼痛有关的刺激诱导的神经系统病理生物学提供线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Control of gene transcription by Jun and Fos proteins in the nervous system

Acute and chronic stimulation of somatosensory and visceral nociceptors are followed by induction of immediate-early gene (IEG) encoded transcription factors such as Jun, Fos, and Krox proteins in the central nervous system. Transection of a peripheral nerve also results in IEG expression in the axotomized neurons and synaptically related central neurons. The spatial and temporal patterns in the nervous system of IEG expression, as studied by immunohistochemistry, are complex and depend on the type and intensity of noxious stimulation. Immediate-early gene encoded proteins control the transcription of other target genes, a few of which have been identified. The authors hypothesize that activations of IEGs represent steps in the transmission of the noxious afferent input into long-lasting alterations of the neuronal cell program. Thus, stimulation induced changes in gene expression may alter the phenotype of neurons, which implies pathophysiologic modifications of neuron function. Immediate-early gene expression is meaningful beyond its present use in the neurosciences as markers of neuronal activity, because it may provide a clue to the understanding of stimulation-induced pathobiology of the nervous system that is involved in the chronicity of pain.

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