Department of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, 60611.
Department of Physiology, School of Basic Medicine, Qingdao University, Qingdao, China, 266071.
J Neurosci. 2021 May 5;41(18):3966-3987. doi: 10.1523/JNEUROSCI.2306-20.2021. Epub 2021 Mar 17.
The classic basal ganglia circuit model asserts a complete segregation of the two striatal output pathways. Empirical data argue that, in addition to indirect-pathway striatal projection neurons (iSPNs), direct-pathway striatal projection neurons (dSPNs) innervate the external globus pallidus (GPe). However, the functions of the latter were not known. In this study, we interrogated the organization principles of striatopallidal projections and their roles in full-body movement in mice (both males and females). In contrast to the canonical motor-promoting response of dSPNs in the dorsomedial striatum (dSPNs), optogenetic stimulation of dSPNs in the dorsolateral striatum (dSPNs) suppressed locomotion. Circuit analyses revealed that dSPNs selectively target Npas1 neurons in the GPe. In a chronic 6-hydroxydopamine lesion model of Parkinson's disease, the dSPN-Npas1 projection was dramatically strengthened. As dSPN-Npas1 projection suppresses movement, the enhancement of this projection represents a circuit mechanism for the hypokinetic symptoms of Parkinson's disease that has not been previously considered. In sum, our results suggest that dSPN input to the GPe is a critical circuit component that is involved in the regulation of movement in both healthy and parkinsonian states. In the classic basal ganglia model, the striatum is described as a divergent structure: it controls motor and adaptive functions through two segregated, opposing output streams. However, the experimental results that show the projection from direct-pathway neurons to the external pallidum have been largely ignored. Here, we showed that this striatopallidal subpathway targets a select subset of neurons in the external pallidum and is motor-suppressing. We found that this subpathway undergoes changes in a Parkinson's disease model. In particular, our results suggest that the increase in strength of this subpathway contributes to the slowness or reduced movements observed in Parkinson's disease.
经典的基底神经节回路模型断言两条纹状体输出途径完全分离。经验数据表明,除了间接通路纹状体投射神经元(iSPNs)外,直接通路纹状体投射神经元(dSPNs)也投射到外苍白球(GPe)。然而,后者的功能尚不清楚。在这项研究中,我们探讨了纹状体苍白球投射的组织原则及其在小鼠(雄性和雌性)全身运动中的作用。与背内侧纹状体(dSPNs)中 dSPNs 的典型促进运动反应相反,背外侧纹状体(dSPNs)中的光遗传学刺激 dSPNs 抑制了运动。回路分析表明,dSPNs 选择性地靶向 GPe 中的 Npas1 神经元。在帕金森病的慢性 6-羟多巴胺损伤模型中,dSPN-Npas1 投射显著增强。由于 dSPN-Npas1 投射抑制运动,因此该投射的增强代表了帕金森病运动减少症状的一种以前未被考虑的回路机制。总之,我们的结果表明,dSPN 对 GPe 的输入是一个关键的回路组成部分,它参与了健康和帕金森病状态下的运动调节。在经典的基底神经节模型中,纹状体被描述为一个发散的结构:它通过两个分离的、对立的输出流来控制运动和适应性功能。然而,显示直接通路神经元投射到外苍白球的实验结果在很大程度上被忽视了。在这里,我们表明这条纹状体苍白球亚通路靶向外苍白球中的一个选定的神经元子集,并具有抑制运动的作用。我们发现这条亚通路在帕金森病模型中发生了变化。特别是,我们的结果表明,这条亚通路的强度增加有助于帕金森病中观察到的运动缓慢或减少。