Negyessy Laszlo, Goldman-Rakic Patricia S
Department of Neurobiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
J Comp Neurol. 2005 Aug 8;488(4):464-75. doi: 10.1002/cne.20601.
Structures of the cerebral cortex expressing the D2 dopamine receptor subtype (D2) are important sites of action of antipsychotic drugs. It has also been repeatedly suggested that the prefrontal cortex plays a significant role in neuropsychiatric disorders, including schizophrenia. Here, by using single and double immunohistochemical techniques with electron microscopy, we investigated in the primate prefrontal cortex the ultrastructural localization of D2 and we compared it with that of the neuronal calcium sensor-1 (NCS-1), a neuron-specific calcium-binding and D2-interacting protein. D2 immunoreactivity, revealed with preembedding immunoperoxidase in single labeling and with preembedding immunogold for double labeling, was localized in cell bodies with ultrastructural characteristics of both neurons and astroglia. D2 was localized in pre- and postsynaptic structures, including spines and dendrites, and in both excitatory- and inhibitory-like axon terminals. Immunogold labeling revealed peri- and extrasynaptic localization of D2 in postsynaptic structures, whereas extrasynaptic labeling was typically found in boutons. NSC-1 immunoreactivity was abundant in pre- and postsynaptic structures, in which it was also colocalized with D2. With the present strategy (that has high resolution but relatively limited sensitivity), NSC-1 was observed in about 10% of the D2-immunopositive spines and in a lower proportion of D2-immunopositive dendrites and boutons. The data demonstrate the localization of D2 in pre- and postsynaptic as well as extra- and perisynaptic structures of the primate prefrontal cortex. The data also show the coexistence of NCS-1 and D2 at the ultrastructural level. The latter finding suggests a role for NCS-1 in desensitization of D2 in the prefrontal cortex.
表达D2多巴胺受体亚型(D2)的大脑皮质结构是抗精神病药物的重要作用位点。也有人反复提出,前额叶皮质在包括精神分裂症在内的神经精神疾病中起重要作用。在此,我们通过使用单重和双重免疫组织化学技术结合电子显微镜,研究了灵长类动物前额叶皮质中D2的超微结构定位,并将其与神经元钙传感器-1(NCS-1)进行比较,NCS-1是一种神经元特异性钙结合蛋白且与D2相互作用。单标记时采用包埋前免疫过氧化物酶法、双重标记时采用包埋前免疫金法显示的D2免疫反应性,定位于具有神经元和星形胶质细胞超微结构特征的细胞体中。D2定位于突触前和突触后结构,包括棘突和树突,以及兴奋性和抑制性样轴突终末。免疫金标记显示D2在突触后结构中位于突触周和突触外,而突触外标记通常见于轴突终扣。NSC-1免疫反应性在前突触和后突触结构中丰富,且也与D2共定位。采用本策略(具有高分辨率但相对有限的敏感性),在约10%的D2免疫阳性棘突中观察到NSC-1,在比例较低的D2免疫阳性树突和轴突终扣中也观察到NSC-1。这些数据证明了D2在灵长类动物前额叶皮质突触前、突触后以及突触外和突触周结构中的定位。数据还显示了NSC-1和D2在超微结构水平上的共存。后一发现提示NSC-1在前额叶皮质中对D2脱敏起作用。