Division of Neuropharmacology and Neurological Diseases, Yerkes National Primate Research Center, Emory University, Atlanta, GA 30329, USA.
UDALL Center for Excellence for Parkinson's Disease, Emory University, Atlanta, GA 30329, USA.
Cereb Cortex. 2021 Jun 10;31(7):3408-3425. doi: 10.1093/cercor/bhab020.
The synaptic organization of thalamic inputs to motor cortices remains poorly understood in primates. Thus, we compared the regional and synaptic connections of vGluT2-positive thalamocortical glutamatergic terminals in the supplementary motor area (SMA) and the primary motor cortex (M1) between control and MPTP-treated parkinsonian monkeys. In controls, vGluT2-containing fibers and terminal-like profiles invaded layer II-III and Vb of M1 and SMA. A significant reduction of vGluT2 labeling was found in layer Vb, but not in layer II-III, of parkinsonian animals, suggesting a potential thalamic denervation of deep cortical layers in parkinsonism. There was a significant difference in the pattern of synaptic connectivity in layers II-III, but not in layer Vb, between M1 and SMA of control monkeys. However, this difference was abolished in parkinsonian animals. No major difference was found in the proportion of perforated versus macular post-synaptic densities at thalamocortical synapses between control and parkinsonian monkeys in both cortical regions, except for a slight increase in the prevalence of perforated axo-dendritic synapses in the SMA of parkinsonian monkeys. Our findings suggest that disruption of the thalamic innervation of M1 and SMA may underlie pathophysiological changes of the motor thalamocortical loop in the state of parkinsonism.
在灵长类动物中,丘脑传入运动皮质的突触组织仍知之甚少。因此,我们比较了正常和 MPTP 处理的帕金森猴运动前区(SMA)和初级运动皮质(M1)中 vGluT2 阳性丘脑皮质谷氨酸能末梢的区域和突触连接。在对照组中,含有 vGluT2 的纤维和末梢样轮廓侵入 M1 和 SMA 的 II-III 层和 Vb 层。帕金森动物的 Vb 层中 vGluT2 标记明显减少,但 II-III 层没有,这表明帕金森病中深部皮质层可能存在丘脑去神经支配。在正常猴的 M1 和 SMA 的 II-III 层中,突触连接模式存在显著差异,但在 Vb 层中没有。然而,这种差异在帕金森动物中消失了。在这两个皮质区域,除了帕金森猴 SMA 中穿孔轴突-树突突触的流行略有增加外,在控制组和帕金森组的丘脑皮质突触中,穿孔与斑状突触后密度的比例没有发现主要差异。我们的研究结果表明,M1 和 SMA 的丘脑传入神经的破坏可能是帕金森状态下运动丘脑皮质回路的病理生理变化的基础。