Noaín Daniela, Avale M Elena, Wedemeyer Carolina, Calvo Daniel, Peper Marcela, Rubinstein Marcelo
Instituto de Investigaciones en Ingeniería Genética y Biología Molecular, Consejo Nacional de Investigaciones Científicas y Técnicas, Vuelta de Obligado 2490, 1428 Buenos Aires, Argentina.
Eur J Neurosci. 2006 Nov;24(9):2429-38. doi: 10.1111/j.1460-9568.2006.05148.x.
The dopamine D4 receptor (D4R) has received considerable interest because of its higher affinity for atypical antipsychotics, the extremely polymorphic nature of the human gene and the genetic association with attention deficit and hyperactivity disorder (ADHD). Several efforts have been undertaken to determine the D4R expression pattern in the brain using immunohistochemistry, binding autoradiography and in situ hybridization, but the overall published results present large discrepancies. Here, we have explored an alternative genetic approach by studying bacterial artificial chromosome (BAC) transgenic mice that express enhanced green fluorescent protein (EGFP) under the transcriptional control of the mouse dopamine D4 receptor gene (Drd4). Immunohistochemical analysis performed in brain sections of Drd4-EGFP transgenic mice using an anti-EGFP polyclonal antibody showed that transgenic expression was predominant in deep layer neurons of the prefrontal cortex, particularly in the orbital, prelimbic, cingulate and rostral agranular portions. In addition, discrete groups of Drd4-EGFP labelled neurons were observed in the anterior olfactory nucleus, ventral pallidum, and lateral parabrachial nucleus. EGFP was not detected in the striatum, hippocampus or midbrain as described using other techniques. Given the fine specificity of EGFP expression in BAC transgenic mice and the high sensitivity of the EGFP antibody used in this study, our results indicate that Drd4 expression in the adult mouse brain is limited to a more restricted number of areas than previously reported. Its leading expression in the prefrontal cortex supports the importance of the D4R in complex behaviours depending on cortical dopamine (DA) transmission and its possible role in the etiopathophysiology of ADHD.
多巴胺D4受体(D4R)因其对非典型抗精神病药物具有更高的亲和力、人类基因的高度多态性以及与注意力缺陷多动障碍(ADHD)的遗传关联而备受关注。人们已经进行了多项努力,使用免疫组织化学、结合放射自显影和原位杂交来确定D4R在大脑中的表达模式,但总体发表的结果存在很大差异。在这里,我们通过研究细菌人工染色体(BAC)转基因小鼠探索了一种替代的遗传学方法,这些小鼠在小鼠多巴胺D4受体基因(Drd4)的转录控制下表达增强型绿色荧光蛋白(EGFP)。使用抗EGFP多克隆抗体对Drd4-EGFP转基因小鼠脑切片进行的免疫组织化学分析表明,转基因表达在前额叶皮质深层神经元中占主导地位,特别是在眶额、前边缘、扣带回和喙部无颗粒部分。此外,在前嗅核、腹侧苍白球和外侧臂旁核中观察到离散的Drd4-EGFP标记神经元群。如使用其他技术所描述的那样,在纹状体、海马体或中脑中未检测到EGFP。鉴于BAC转基因小鼠中EGFP表达的精细特异性以及本研究中使用的EGFP抗体的高灵敏度,我们的结果表明,成年小鼠脑中Drd4的表达仅限于比先前报道的更有限的区域。它在前额叶皮质中的主要表达支持了D4R在依赖于皮质多巴胺(DA)传递的复杂行为中的重要性及其在ADHD病因病理生理学中的可能作用。