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GPR151受体在脊椎动物缰核轴突投射中的保守表达。

Conserved expression of the GPR151 receptor in habenular axonal projections of vertebrates.

作者信息

Broms Jonas, Antolin-Fontes Beatriz, Tingström Anders, Ibañez-Tallon Ines

机构信息

Psychiatric Neuromodulation Unit, Clinical Sciences, Lund University, 222 42, Lund, Sweden.

出版信息

J Comp Neurol. 2015 Feb 15;523(3):359-80. doi: 10.1002/cne.23664. Epub 2014 Sep 8.

Abstract

The habenula is a phylogenetically conserved brain structure in the epithalamus. It is a major node in the information flow between fronto-limbic brain regions and monoaminergic brainstem nuclei, and is thus anatomically and functionally ideally positioned to regulate emotional, motivational, and cognitive behaviors. Consequently, the habenula may be critically important in the pathophysiology of psychiatric disorders such as addiction and depression. Here we investigated the expression pattern of GPR151, a G protein-coupled receptor (GPCR), whose mRNA has been identified as highly and specifically enriched in habenular neurons by in situ hybridization and translating ribosome affinity purification (TRAP). In the present immunohistochemical study we demonstrate a pronounced and highly specific expression of the GPR151 protein in the medial and lateral habenula of rodent brain. Specific expression was also seen in efferent habenular fibers projecting to the interpeduncular nucleus, the rostromedial tegmental area, the rhabdoid nucleus, the mesencephalic raphe nuclei, and the dorsal tegmental nucleus. Using confocal microscopy and quantitative colocalization analysis, we found that GPR151-expressing axons and terminals overlap with cholinergic, substance P-ergic, and glutamatergic markers. Virtually identical expression patterns were observed in rat, mouse, and zebrafish brains. Our data demonstrate that GPR151 is highly conserved, specific for a subdivision of the habenular neurocircuitry, and constitutes a promising novel target for psychiatric drug development.

摘要

缰核是上丘脑一个在系统发育上保守的脑结构。它是额叶-边缘脑区与单胺能脑干核团之间信息流的主要节点,因此在解剖学和功能上处于调节情绪、动机和认知行为的理想位置。因此,缰核在成瘾和抑郁等精神疾病的病理生理学中可能至关重要。在这里,我们研究了GPR151(一种G蛋白偶联受体(GPCR))的表达模式,通过原位杂交和翻译核糖体亲和纯化(TRAP)已确定其mRNA在缰核神经元中高度且特异性富集。在本免疫组织化学研究中,我们证明了GPR151蛋白在啮齿动物脑的内侧和外侧缰核中显著且高度特异性表达。在投射到脚间核、嘴内侧被盖区、横纹肌样核、中脑缝际核和背侧被盖核的传出缰核纤维中也可见特异性表达。使用共聚焦显微镜和定量共定位分析,我们发现表达GPR151的轴突和终末与胆碱能、P物质能和谷氨酸能标记物重叠。在大鼠、小鼠和斑马鱼脑中观察到几乎相同的表达模式。我们的数据表明,GPR151高度保守,对缰核神经回路的一个细分具有特异性,并且构成了精神药物开发的一个有前景的新靶点。

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