Evangelio Marian, García-Amado María, Clascá Francisco
Department of Anatomy and Neuroscience, School of Medicine, Autonomous University of Madrid, Madrid, Spain.
Front Neuroanat. 2018 Apr 12;12:27. doi: 10.3389/fnana.2018.00027. eCollection 2018.
A key parameter to constrain predictive, bottom-up circuit models of a given brain domain is the number and position of the neuronal populations involved. These include not only the neurons whose bodies reside within the domain, but also the neurons in distant regions that innervate the domain. The mouse visual cortex receives its main subcortical input from the dorsal lateral geniculate nucleus (dLGN) and the lateral posterior (LP) complex of the thalamus. The latter consists of three different nuclei: lateral posterior lateral (LPL), lateral posterior medial rostral (LPMR), and lateral posterior medial caudal (LPMC), each exhibiting specific patterns of connections with the various visual cortical areas. Here, we have determined the number of thalamocortical projection neurons and interneurons in the LP complex and dLGN of the adult C57BL/6 male mouse. We combined Nissl staining and histochemical and immunolabeling methods for consistently delineating nuclei borders, and applied unbiased stereological cell counting methods. Thalamic interneurons were identified using GABA immunolabeling. The C57BL/6 dLGN contains ∼21,200 neurons, while LP complex contains ∼31,000 total neurons. The dLGN and LP are the only nuclei of the mouse dorsal thalamus containing substantial numbers GABA-immunoreactive interneurons. These interneurons, however, are scarcer than previously estimated; they are 5.6% of dLGN neurons and just 1.9% of the LP neurons. It can be thus inferred that the dLGN contains ∼20,000 and the LP complex ∼30,400 thalamocortical projection neurons (∼12,000 in LPL, 15,200 in LPMR, and 4,200 in LPMC). The present dataset is relevant for constraining models of mouse visual thalamocortical circuits, as well as for quantitative comparisons between genetically modified mouse strains, or across species.
限制给定脑区预测性、自下而上的回路模型的一个关键参数是所涉及神经元群体的数量和位置。这些群体不仅包括其胞体位于该脑区内的神经元,还包括支配该脑区的远处区域的神经元。小鼠视觉皮层主要从丘脑背外侧膝状体核(dLGN)和丘脑外侧后核(LP)复合体接收皮层下输入。后者由三个不同的核组成:外侧后外侧核(LPL)、外侧后内侧吻侧核(LPMR)和外侧后内侧尾侧核(LPMC),每个核都与不同的视觉皮层区域呈现出特定的连接模式。在这里,我们确定了成年C57BL/6雄性小鼠LP复合体和dLGN中丘脑皮质投射神经元和中间神经元的数量。我们结合了尼氏染色以及组织化学和免疫标记方法来一致地描绘核边界,并应用了无偏立体细胞计数方法。使用GABA免疫标记来识别丘脑中间神经元。C57BL/6小鼠的dLGN包含约21,200个神经元,而LP复合体总共包含约31,000个神经元。dLGN和LP是小鼠背侧丘脑中仅有的含有大量GABA免疫反应性中间神经元的核。然而这些中间神经元比之前估计得更为稀少;它们占dLGN神经元数量的5.6%,仅占LP神经元数量 的1.9%。由此可以推断,dLGN包含约20,000个丘脑皮质投射神经元,LP复合体包含约30,400个丘脑皮质投射神经元(LPL中有12,000个,LPMR中有15,200个,LPMC中有4,200个)。本数据集对于限制小鼠视觉丘脑皮质回路模型以及在转基因小鼠品系之间或跨物种进行定量比较具有重要意义。