Hersch S M, Ciliax B J, Gutekunst C A, Rees H D, Heilman C J, Yung K K, Bolam J P, Ince E, Yi H, Levey A I
Department of Neurology, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
J Neurosci. 1995 Jul;15(7 Pt 2):5222-37. doi: 10.1523/JNEUROSCI.15-07-05222.1995.
The precise localization of D1 and D2 dopamine receptors within striatal neurons and circuits is crucial information for further understanding dopamine pharmacology. We have used subtype specific polyclonal and monoclonal antibodies against D1 and D2 dopamine receptors to determine their cellular and subcellular distributions, their colocalization, and their differential connectivity with motor cortical afferents labeled either by lesion-induced degeneration or by anterograde transport of biotinylated dextrans. D1 and D2 are primarily expressed in medium-sized neurons and spiny dendrites. Axon terminals containing D1 were rare whereas D2-immunoreactive axon terminals forming symmetrical synapses with dendrites and spines were common. In 2 microns sections, D1 was localized to 53% of neurons, and D2 to 48% of neurons, while mixing D1 and D2 antibodies labeled 78%. By electron microscopy, D1 was localized to 43% of dendrites and 38% of spines while D2 was localized to 38% of dendrites and 48% of spines. Combining D1 and D2 antibodies resulted in the labeling of 88.5% of dendrites and 92.6% of spines. Using different chromogens for D1 and D2, colocalization was not observed. Ipsilateral motor corticostriatal afferents were primarily axospinous and significantly more synapsed with D1 than D2-positive spines (65% vs 47%). Contralateral motor corticostriatal afferents were frequently axodendritic and no difference in their frequency of synapses with D1 and D2 dendrites and spines was observed. These findings demonstrate differential patterns of expression of D1 and D2 receptors in striatal neurons and axon terminals and their differential involvement in motor corticostriatal circuits.
D1和D2多巴胺受体在纹状体神经元及神经回路中的精确定位,对于进一步理解多巴胺药理学至关重要。我们使用了针对D1和D2多巴胺受体的亚型特异性多克隆和单克隆抗体,来确定它们在细胞和亚细胞水平的分布、共定位情况,以及它们与通过损伤诱导变性或生物素化葡聚糖的顺行转运标记的运动皮质传入纤维的差异连接。D1和D2主要表达于中等大小的神经元和有棘树突。含有D1的轴突终末很少见,而与树突和棘形成对称突触的D2免疫反应性轴突终末很常见。在2微米厚的切片中,D1定位于53%的神经元,D2定位于48%的神经元,而混合使用D1和D2抗体标记了78%的神经元。通过电子显微镜观察,D1定位于38%的树突和43%的棘,而D2定位于38%的树突和48%的棘。联合使用D1和D2抗体导致88.5%的树突和92.6%的棘被标记。使用针对D1和D2的不同显色剂,未观察到共定位现象。同侧运动皮质纹状体传入纤维主要是轴棘突触,与D1阳性棘形成突触的比例显著高于D2阳性棘(65%对47%)。对侧运动皮质纹状体传入纤维常为轴树突触,未观察到它们与D1和D2树突及棘形成突触的频率有差异。这些发现表明D1和D2受体在纹状体神经元和轴突终末中存在差异表达模式,以及它们在运动皮质纹状体神经回路中的不同参与情况。