Takada Masahiko
Systems Neuroscience Section, Department of Cellular and Molecular Biology, Primate Research Institute, Kyoto University, Japan.
Brain Nerve. 2013 Jun;65(6):635-42.
Using a neuron-specific retrograde gene-transfer vector based on the lentivirus, we established immunotoxin (IT)-mediated tract targeting in the primate brain; this technique allows ablation of a neuronal population constituting a certain pathway. Here, we introduce a recent study on selective removal of the cortico-subthalamic "hyperdirect" pathway. Together with the direct and indirect pathways, the hyperdirect pathway plays a crucial role in motor information processing in the basal ganglia. This pathway links the motor-related areas of the frontal lobe directly to the subthalamic nucleus (STN) without relay at the striatum. After electrical stimulation of the motor-related areas, such as the supplementary motor area (SMA), triphasic responses consisting of an early excitation, an inhibition, and a late excitation are usually detected in the internal segment of the globus pallidus (GPi). Several lines of evidence suggest that the early excitation may be derived from the hyperdirect pathway. We injected the lentiviral vector expressing human interleukin-2 receptor α-subunit into the monkey STN. IT was then injected into the SMA. We recorded GPi neuron responses to SMA stimulation. We found that the early excitation was reduced neither with the inhibition nor with the late excitation. The spontaneous firing rate and pattern of GPi neurons remained unchanged. This indicated that IT-mediated tract targeting successfully and selectively eliminated the hyperdirect pathway from the basal ganglia circuitry without affecting the spontaneous activity of STN neurons. This electrophysiological finding was confirmed using anatomical data obtained from retrograde and anterograde neural tracings. The present results show that the cortically driven early excitation in GPi neurons is mediated by the hyperdirect pathway. The IT-mediated tract targeting technique will provide us with novel strategies for elucidating various neural network functions.
我们使用基于慢病毒的神经元特异性逆行基因转移载体,在灵长类动物大脑中建立了免疫毒素(IT)介导的神经束靶向;该技术能够消融构成特定通路的神经元群体。在此,我们介绍一项关于选择性去除皮质 - 丘脑底核“超直接”通路的最新研究。超直接通路与直接和间接通路一起,在基底神经节的运动信息处理中起着关键作用。该通路将额叶的运动相关区域直接连接到丘脑底核(STN),而无需在纹状体中继。在对运动相关区域(如辅助运动区(SMA))进行电刺激后,通常在苍白球内侧部(GPi)检测到由早期兴奋、抑制和晚期兴奋组成的三相反应。有几条证据表明早期兴奋可能源自超直接通路。我们将表达人白细胞介素 - 2受体α亚基的慢病毒载体注入猴子的STN。然后将IT注入SMA。我们记录了GPi神经元对SMA刺激的反应。我们发现早期兴奋既没有随着抑制也没有随着晚期兴奋而降低。GPi神经元的自发放电率和模式保持不变。这表明IT介导的神经束靶向成功且选择性地从基底神经节回路中消除了超直接通路,而不影响STN神经元的自发活动。使用从逆行和顺行神经追踪获得的解剖学数据证实了这一电生理学发现。目前的结果表明,GPi神经元中由皮质驱动的早期兴奋是由超直接通路介导的。IT介导的神经束靶向技术将为我们阐明各种神经网络功能提供新的策略。