Abdi Azzedine, Mallet Nicolas, Mohamed Foad Y, Sharott Andrew, Dodson Paul D, Nakamura Kouichi C, Suri Sana, Avery Sophie V, Larvin Joseph T, Garas Farid N, Garas Shady N, Vinciati Federica, Morin Stéphanie, Bezard Erwan, Baufreton Jérôme, Magill Peter J
Université de Bordeaux, Institut des Maladies Neurodégénératives, F-33000 Bordeaux, France, Centre National de la Recherche Scientifique Unité Mixte de Recherche 5293, Institut des Maladies Neurodégénératives, F-33000 Bordeaux, France.
Université de Bordeaux, Institut des Maladies Neurodégénératives, F-33000 Bordeaux, France, Centre National de la Recherche Scientifique Unité Mixte de Recherche 5293, Institut des Maladies Neurodégénératives, F-33000 Bordeaux, France, Medical Research Council Brain Network Dynamics Unit, Department of Pharmacology, University of Oxford, Oxford OX1 3QT, United Kingdom, and.
J Neurosci. 2015 Apr 29;35(17):6667-88. doi: 10.1523/JNEUROSCI.4662-14.2015.
Studies in dopamine-depleted rats indicate that the external globus pallidus (GPe) contains two main types of GABAergic projection cell; so-called "prototypic" and "arkypallidal" neurons. Here, we used correlative anatomical and electrophysiological approaches in rats to determine whether and how this dichotomous organization applies to the dopamine-intact GPe. Prototypic neurons coexpressed the transcription factors Nkx2-1 and Lhx6, comprised approximately two-thirds of all GPe neurons, and were the major GPe cell type innervating the subthalamic nucleus (STN). In contrast, arkypallidal neurons expressed the transcription factor FoxP2, constituted just over one-fourth of GPe neurons, and innervated the striatum but not STN. In anesthetized dopamine-intact rats, molecularly identified prototypic neurons fired at relatively high rates and with high regularity, regardless of brain state (slow-wave activity or spontaneous activation). On average, arkypallidal neurons fired at lower rates and regularities than prototypic neurons, and the two cell types could be further distinguished by the temporal coupling of their firing to ongoing cortical oscillations. Complementing the activity differences observed in vivo, the autonomous firing of identified arkypallidal neurons in vitro was slower and more variable than that of prototypic neurons, which tallied with arkypallidal neurons displaying lower amplitudes of a "persistent" sodium current important for such pacemaking. Arkypallidal neurons also exhibited weaker driven and rebound firing compared with prototypic neurons. In conclusion, our data support the concept that a dichotomous functional organization, as actioned by arkypallidal and prototypic neurons with specialized molecular, structural, and physiological properties, is fundamental to the operations of the dopamine-intact GPe.
对多巴胺耗竭大鼠的研究表明,外侧苍白球(GPe)包含两种主要类型的γ-氨基丁酸能投射细胞;即所谓的“原型”和“原苍白球”神经元。在此,我们采用相关的解剖学和电生理学方法研究大鼠,以确定这种二分组织是否以及如何适用于多巴胺功能正常的GPe。原型神经元共表达转录因子Nkx2-1和Lhx6,约占所有GPe神经元的三分之二,是支配丘脑底核(STN)的主要GPe细胞类型。相比之下,原苍白球神经元表达转录因子FoxP2,占GPe神经元的四分之一多一点,支配纹状体但不支配STN。在麻醉状态下多巴胺功能正常的大鼠中,分子鉴定的原型神经元无论脑状态(慢波活动或自发激活)如何,均以相对较高的频率和高度规律性放电。平均而言,原苍白球神经元放电频率和规律性低于原型神经元,并且这两种细胞类型可通过其放电与持续的皮层振荡的时间耦合进一步区分。与体内观察到的活动差异相一致,体外鉴定的原苍白球神经元的自主放电比原型神经元更慢且更具变异性,这与原苍白球神经元表现出较低幅度的对这种起搏很重要的“持续性”钠电流相符。与原型神经元相比,原苍白球神经元还表现出较弱的驱动性和反弹放电。总之,我们的数据支持这样一种概念,即由具有特殊分子、结构和生理特性的原苍白球和原型神经元所执行的二分功能组织,是多巴胺功能正常的GPe运作的基础。