Yerkes National Primate Research Center, Atlanta, Georgia, USA.
UDALL Center of Excellence for Parkinson's Disease, Atlanta, Georgia, USA.
J Comp Neurol. 2021 May 1;529(7):1703-1718. doi: 10.1002/cne.25051. Epub 2020 Oct 20.
The glutamate receptor delta 1 (GluD1) is strongly expressed in the striatum. Knockout of GluD1 expression in striatal neurons elicits cognitive deficits and disrupts the thalamostriatal system in mice. To understand the potential role of GluD1 in the primate striatum, we compared the cellular and subcellular localization of striatal GluD1 immunoreactivity (GluD1-IR) in mice and monkeys. In both species, striatal GluD1-IR displayed a patchy pattern of distribution in register with the striosome/matrix compartmentation, but in an opposite fashion. While GluD1 was more heavily expressed in the striosomes than the matrix in the monkey caudate nucleus, the opposite was found in the mouse striatum. At the electron microscopic level, GluD1-IR was preferentially expressed in dendritic shafts (47.9 ± 1.2%), followed by glia (37.7 ± 2.5%), and dendritic spines (14.3 ± 2.6%) in the matrix of the mouse striatum. This pattern was not statistically different from the labeling in the striosome and matrix compartments of the monkey caudate nucleus, with the exception of a small amount of GluD1-positive unmyelinated axons and axon terminals in the primate striatum. Immunogold staining revealed synaptic and perisynaptic GluD1 labeling at putative axo-dendritic and axo-spinous glutamatergic synapses, and intracellular labeling on the surface of mitochondria. Confocal microscopy showed that GluD1 is preferentially colocalized with thalamic over cortical terminals in both the striosome and matrix compartments. These data provide the anatomical substrate for a deeper understanding of GluD1 regulation of striatal glutamatergic synapses, but also suggest possible extrasynaptic, glial, and mitochondrial GluD1 functions.
谷氨酸受体 delta 1 (GluD1) 在纹状体中表达强烈。在纹状体神经元中敲除 GluD1 的表达会引起认知缺陷,并破坏小鼠的丘脑纹状体系统。为了了解 GluD1 在灵长类动物纹状体中的潜在作用,我们比较了小鼠和猴子纹状体中 GluD1 免疫反应性 (GluD1-IR) 的细胞和亚细胞定位。在这两种物种中,纹状体的 GluD1-IR 呈现出与纹状体/基质分隔一致的斑块状分布模式,但方式相反。在猴尾状核中,GluD1 在纹状体中的表达比基质更重,而在鼠纹状体中则相反。在电子显微镜水平,GluD1-IR 主要表达在树突干 (47.9 ± 1.2%),其次是胶质细胞 (37.7 ± 2.5%),和树突棘 (14.3 ± 2.6%)在鼠纹状体的基质中。这种模式与猴尾状核纹状体和基质隔室的标记没有统计学差异,除了在灵长类动物纹状体中有少量的 GluD1 阳性无髓轴突和轴突末梢。免疫金染色显示突触和突触周 GluD1 标记在假定的轴突-树突和轴突-棘突谷氨酸能突触上,以及线粒体外表面的细胞内标记。共聚焦显微镜显示,GluD1 优先与丘脑而不是皮质末梢共定位,无论是在纹状体还是基质隔室中。这些数据为深入了解 GluD1 对纹状体谷氨酸能突触的调节提供了解剖学基础,但也提示了可能的突触外、胶质和线粒体 GluD1 功能。