Sesack S R, Hawrylak V A, Matus C, Guido M A, Levey A I
Department of Neuroscience and Psychiatry, University of Pittsburgh, Pennsylvania 15260, USA.
J Neurosci. 1998 Apr 1;18(7):2697-708. doi: 10.1523/JNEUROSCI.18-07-02697.1998.
The dopamine transporter (DAT) critically regulates the duration of the cellular actions of dopamine and the extent to which dopamine diffuses in the extracellular space. We sought to determine whether the reportedly greater diffusion of dopamine in the rat prefrontal cortex (PFC) as compared with the striatum is associated with a more restricted axonal distribution of the cortical DAT protein. By light microscopy, avidin-biotin-peroxidase immunostaining for DAT was visualized in fibers that were densely distributed within the dorsolateral striatum and the superficial layers of the dorsal anterior cingulate cortex. In contrast, DAT-labeled axons were distributed only sparsely to the deep layers of the prelimbic cortex. By electron microscopy, DAT-immunoreactive profiles in the striatum and cingulate cortex included both varicose and intervaricose segments of axons. However, DAT-labeled processes in the prelimbic cortex were almost exclusively intervaricose axon segments. Immunolabeling for tyrosine hydroxylase in adjacent sections of the prelimbic cortex was localized to both varicosities and intervaricose segments of axons. These qualitative observations were supported by a quantitative assessment in which the diameter of immunoreactive profiles was used as a relative measure of whether varicose or intervaricose axon segments were labeled. These results suggest that considerable extracellular diffusion of dopamine in the prelimbic PFC may result, at least in part, from a paucity of DAT content in mesocortical dopamine axons, as well as a distribution of the DAT protein at a distance from synaptic release sites. The results further suggest that different populations of dopamine neurons selectively target the DAT to different subcellular locations.
多巴胺转运体(DAT)对多巴胺细胞作用的持续时间以及多巴胺在细胞外空间的扩散程度起着关键调节作用。我们试图确定,与纹状体相比,据报道多巴胺在大鼠前额叶皮质(PFC)中更大程度的扩散是否与皮质DAT蛋白轴突分布的更受限有关。通过光学显微镜观察,用抗生物素蛋白-生物素-过氧化物酶对DAT进行免疫染色,在背外侧纹状体和背侧前扣带回皮质浅层内密集分布的纤维中可见。相比之下,DAT标记的轴突仅稀疏地分布于前边缘皮质深层。通过电子显微镜观察,纹状体和扣带回皮质中DAT免疫反应性结构包括轴突的曲张段和曲张段之间的部分。然而,前边缘皮质中DAT标记的结构几乎完全是轴突曲张段之间的部分。在前边缘皮质相邻切片中对酪氨酸羟化酶进行免疫标记,其定位于轴突的曲张段和曲张段之间的部分。这些定性观察结果得到了定量评估的支持,在该评估中,免疫反应性结构的直径被用作标记的是曲张轴突段还是曲张段之间轴突段的相对指标。这些结果表明,前边缘PFC中多巴胺在细胞外的大量扩散可能至少部分是由于中皮质多巴胺轴突中DAT含量稀少,以及DAT蛋白在远离突触释放位点处的分布所致。结果还表明,不同群体的多巴胺神经元将DAT选择性地靶向不同的亚细胞位置。