Department of Anatomy & Neuroscience, Autónoma de Madrid University, Madrid E28029, Spain.
Department of Neuroinformatics, Donders Centre for Neuroscience, Radboud University Nijmegen, Nijmegen 6525 AJ, The Netherlands.
J Neurosci. 2024 Oct 23;44(43):e1096242024. doi: 10.1523/JNEUROSCI.1096-24.2024.
Thalamocortical pathways from the rodent ventral posterior (VP) thalamic complex to the somatosensory cerebral cortex areas are a key model in modern neuroscience. However, beyond the intensively studied projection from medial VP (VPM) to the primary somatosensory area (S1), the wiring of these pathways remains poorly characterized. We combined micropopulation tract-tracing and single-cell transfection experiments to map the pathways arising from different portions of the VP complex in male mice. We found that pathways originating from different VP regions show differences in area/lamina arborization pattern and axonal varicosity size. Neurons from the rostral VPM subnucleus innervate trigeminal S1 in point-to-point fashion. In contrast, a caudal VPM subnucleus innervates heavily and topographically second somatosensory area (S2), but not S1. Neurons in a third, intermediate VPM subnucleus innervate through branched axons both S1 and S2, with markedly different laminar patterns in each area. A small anterodorsal subnucleus selectively innervates dysgranular S1. The parvicellular VPM subnucleus selectively targets the insular cortex and adjacent portions of S1 and S2. Neurons in the rostral part of the lateral VP nucleus (VPL) innervate spinal S1, while caudal VPL neurons simultaneously target S1 and S2. Rostral and caudal VP nuclei show complementary patterns of calcium-binding protein expression. In addition to the cortex, neurons in caudal VP subnuclei target the sensorimotor striatum. Our finding of a massive projection from VP to S2 separate from the VP projections to S1 adds critical anatomical evidence to the notion that different somatosensory submodalities are processed in parallel in S1 and S2.
从啮齿动物腹后核(VP)丘脑复合体到躯体感觉大脑皮层区域的丘脑皮质通路是现代神经科学的一个重要模型。然而,除了从内侧 VP(VPM)到初级躯体感觉区(S1)的强烈研究的投射之外,这些通路的连接仍然知之甚少。我们结合微群体示踪和单细胞转染实验,绘制了雄性小鼠中来自 VP 复合体不同部位的通路图谱。我们发现,来自不同 VP 区域的通路在区域/层树突分支模式和轴突末梢大小上存在差异。来自 VPM 前核亚核的神经元以点对点的方式支配三叉神经 S1。相比之下,VPM 后核亚核大量且拓扑地支配第二躯体感觉区(S2),但不支配 S1。第三中间 VPM 亚核的神经元通过分支轴突支配 S1 和 S2,在每个区域都有明显不同的层模式。一个小的前背亚核选择性支配颗粒状 S1。小细胞 VPM 亚核选择性靶向岛叶皮质和 S1 和 S2 的相邻部分。外侧 VP 核(VPL)的前头部神经元支配脊髓 S1,而尾部 VPL 神经元同时靶向 S1 和 S2。VPL 的前头部和尾部都表现出互补的钙结合蛋白表达模式。除了皮质,尾部 VP 亚核的神经元还靶向感觉运动纹状体。我们发现 VP 到 S2 的大量投射与 VP 到 S1 的投射分离,这为不同躯体感觉亚模式在 S1 和 S2 中并行处理的观点提供了关键的解剖学证据。