Neuroscience Graduate Program, Vanderbilt University, 465 21st Avenue South, Nashville, Tennessee 37232, USA.
Neuroscience. 2011 Dec 29;199:501-14. doi: 10.1016/j.neuroscience.2011.10.004. Epub 2011 Oct 8.
The timeline of dopamine (DA) system maturation and the signaling properties of DA receptors (DRs) during rat brain development are not fully characterized. We used in situ hybridization and quantitative PCR to map DR mRNA transcripts in the medial frontal cortex (mFC) and striatum (STR) of the rat from embryonic day (E) 15 to E21. The developmental trajectory of DR mRNAs revealed distinct patterns of DA receptors 1 and 2 (DRD1, DRD2) in these brain regions. Whereas the mFC had a steeper increase in DRD1 mRNA, the STR had a steeper increase in DRD2 mRNA. Both DR mRNAs were expressed at a higher level in the STR compared with the mFC. To identify the functional properties of DRs during embryonic development, the phosphorylation states of cyclic AMP response element binding protein, extracellular signal-regulated kinase 1/2, and glycogen synthase kinase 3 beta were examined after DR stimulation in primary neuronal cultures obtained from E15 and E18 embryos and cultured for 3 days to ensure a stable baseline level. DR-mediated signaling cascades were functional in E15 cultures in both brain regions. Because DA fibers do not reach the mFC by E15, and DA was not present in cultures, these data indicate that DRs can become functional in the absence of DA innervation. Because activation of DR signal transduction pathways can affect network organization of the developing brain, maternal exposure to drugs that affect DR activity may be liable to interfere with fetal brain development.
多巴胺(DA)系统在大鼠脑发育过程中的成熟时间以及 DA 受体(DR)的信号特性尚未完全阐明。我们使用原位杂交和定量 PCR 来描绘大鼠胚胎期(E)15 至 E21 期间内侧额皮质(mFC)和纹状体(STR)中 DR mRNA 转录本。DR mRNA 的发育轨迹揭示了这些脑区中不同的 DA 受体 1 和 2(DRD1、DRD2)模式。虽然 mFC 中 DRD1 mRNA 的增加更为陡峭,但 STR 中 DRD2 mRNA 的增加更为陡峭。与 mFC 相比,两种 DR mRNA 在 STR 中的表达水平更高。为了在胚胎发育过程中鉴定 DR 的功能特性,在从 E15 和 E18 胚胎获得的原代神经元培养物中刺激 DR 后,检查了环磷酸腺苷反应元件结合蛋白、细胞外信号调节激酶 1/2 和糖原合成酶激酶 3β的磷酸化状态,并培养 3 天以确保稳定的基线水平。在两个脑区的 E15 培养物中,DR 介导的信号级联反应均具有功能。由于 DA 纤维在 E15 时尚未到达 mFC,并且培养物中不存在 DA,因此这些数据表明,在没有 DA 支配的情况下,DR 可以变得具有功能。由于 DR 信号转导途径的激活可以影响发育中大脑的网络组织,因此母体暴露于影响 DR 活性的药物可能容易干扰胎儿大脑发育。