Sánchez Natalia, Coura Renata, Engmann Olivia, Marion-Poll Lucile, Longueville Sophie, Hervé Denis, Andrés María E, Girault Jean-Antoine
Millennium Nucleus in Stress and Addiction (NEDA), Department of Cellular and Molecular Biology, Faculty of Biological Sciences, Pontificia Universidad Católica de Chile, Chile; Inserm, UMR-S 839, Paris, France; Université Pierre et Marie Curie (UPMC), Paris, France; Institut du Fer à Moulin, Paris, France.
Inserm, UMR-S 839, Paris, France; Université Pierre et Marie Curie (UPMC), Paris, France; Institut du Fer à Moulin, Paris, France.
Neuropharmacology. 2014 Apr;79:559-66. doi: 10.1016/j.neuropharm.2014.01.008. Epub 2014 Jan 15.
Impaired dopaminergic signaling in the striatum is involved in diseases as diverse as Parkinson's disease, addiction, and schizophrenia. An important pathophysiological aspect is the loss of balance between striatopallidal and striatonigral pathways. Nur77 is an orphan nuclear receptor and dopamine-regulated immediate-early gene. Classical antipsychotic drugs widely used in the treatment of schizophrenia, such as haloperidol, increase Nur77 mRNA expression in the striatum. However, little is known about the intracellular signaling pathways involved in Nur77 induction. Here, using pharmacological approaches and transgenic mutant mice, we investigated the mechanisms underlying the up-regulation of Nur77 protein expression in the dorsal striatum after haloperidol injection. In drd1a::EGFP transgenic mice that express GFP in D1 neurons, Nur77 up-regulation induced by haloperidol occurred predominantly in GFP-negative neurons. In Gαolf heterozygous mutant mice, in which cAMP production in response to A2A stimulation is impaired in the striatum, haloperidol effect was not altered. In contrast, in DARPP-32 knock-in mutant mice bearing a T34A point mutation of the site responsible for cAMP-dependent phosphatase 1 inhibition, Nur77 up-regulation by haloperidol was prevented. Haloperidol also induced Nur77 protein in D2 neurons of the nucleus accumbens core of wild type but not T34A knock-in mice. Thus, our results show that expression of Nur77 is induced by haloperidol in D2 receptors-expressing medium-sized spiny neurons, through cAMP-dependent regulation of protein phosphatase 1, which is likely to modulate the effects of other protein kinases. Our results clarify the mechanisms of Nur77 induction by antipsychotic and its possible contribution to extrapyramidal effects.
纹状体中多巴胺能信号传导受损与帕金森病、成瘾和精神分裂症等多种疾病有关。一个重要的病理生理学方面是纹状体苍白球和纹状体黑质通路之间平衡的丧失。Nur77是一种孤儿核受体和多巴胺调节的即刻早期基因。广泛用于治疗精神分裂症的经典抗精神病药物,如氟哌啶醇,可增加纹状体中Nur77 mRNA的表达。然而,关于Nur77诱导所涉及的细胞内信号通路知之甚少。在这里,我们使用药理学方法和转基因突变小鼠,研究了氟哌啶醇注射后背侧纹状体中Nur77蛋白表达上调的机制。在D1神经元中表达绿色荧光蛋白(GFP)的drd1a::EGFP转基因小鼠中,氟哌啶醇诱导的Nur77上调主要发生在GFP阴性神经元中。在Gαolf杂合突变小鼠中,纹状体中对A2A刺激的cAMP产生受损,氟哌啶醇的作用未改变。相反,在携带负责cAMP依赖性磷酸酶1抑制位点的T34A点突变的DARPP-32基因敲入突变小鼠中,氟哌啶醇诱导的Nur被阻止上调。氟哌啶醇还在野生型而非T34A基因敲入小鼠伏隔核核心的D2神经元中诱导Nur77蛋白。因此,我们的结果表明,氟哌啶醇在表达D2受体的中等大小棘状神经元中通过cAMP依赖性调节蛋白磷酸酶1诱导Nur77的表达,这可能会调节其他蛋白激酶的作用。我们的结果阐明了抗精神病药物诱导Nur77的机制及其对锥体外系效应的可能贡献。