Sanabria Branden D, Baskar Sindhuja S, Yonk Alex J, Lee Christian R, Margolis David J
bioRxiv. 2023 Mar 6:2023.03.06.531405. doi: 10.1101/2023.03.06.531405.
The anterior dorsolateral striatum (DLS) is heavily innervated by convergent excitatory projections from the primary motor (M1) and sensory cortex (S1) and is considered an important site of sensorimotor integration. M1 and S1 corticostriatal synapses have functional differences in the strength of their connections with striatal spiny projection neurons (SPNs) and fast-spiking interneurons (FSIs) in the DLS, and as a result exert an opposing influence on sensory-guided behaviors. In the present study, we tested whether M1 and S1 inputs exhibit differences in the subcellular anatomical distribution onto striatal neurons. We injected adeno-associated viral vectors encoding spaghetti monster fluorescent proteins (sm.FPs) into M1 and S1, and used confocal microscopy to generate 3D reconstructions of corticostriatal inputs to single identified SPNs and FSIs obtained through ex-vivo patch-clamp electrophysiology. We found that SPNs are less innervated by S1 compared to M1, but FSIs receive a similar number of inputs from both M1 and S1. In addition, M1 and S1 inputs were distributed similarly across the proximal, medial, and distal regions of SPNs and FSIs. Notably, clusters of inputs were prevalent in SPNs but not FSIs. Our results suggest that SPNs have stronger functional connectivity to M1 compared to S1 due to a higher density of synaptic inputs. The clustering of M1 and S1 inputs onto SPNs but not FSIs suggest that cortical inputs are integrated through cell-type specific mechanisms and more generally have implications for how sensorimotor integration is performed in the striatum.
The dorsolateral striatum (DLS) is a key brain area involved in sensorimotor integration due to its dense innervation by the primary motor (M1) and sensory cortex (S1). However, the quantity and anatomical distribution of these inputs to the striatal cell population has not been well characterized. In this study we demonstrate that corticostriatal projections from M1 and S1 differentially innervate spiny projection neurons (SPNs) and fast-spiking interneurons (FSIs) in the DLS. S1 inputs innervate SPNs less than M1 and are likely to form synaptic clusters in SPNs but not in FSIs. These findings suggest that sensorimotor integration is partly achieved by differences in the synaptic organization of corticostriatal inputs to local striatal microcircuits.
背外侧纹状体前部(DLS)接受来自初级运动皮层(M1)和感觉皮层(S1)的汇聚兴奋性投射的大量支配,被认为是感觉运动整合的重要部位。M1和S1皮质纹状体突触在与DLS中纹状体棘状投射神经元(SPN)和快发放中间神经元(FSI)的连接强度上存在功能差异,因此对感觉引导行为产生相反的影响。在本研究中,我们测试了M1和S1输入在纹状体神经元上的亚细胞解剖分布是否存在差异。我们将编码意大利面条怪物荧光蛋白(sm.FPs)的腺相关病毒载体注入M1和S1,并使用共聚焦显微镜对通过离体膜片钳电生理获得的单个已识别SPN和FSI的皮质纹状体输入进行三维重建。我们发现,与M1相比,SPN受S1的支配较少,但FSI从M1和S1接收的输入数量相似。此外,M1和S1输入在SPN和FSI的近端、内侧和远端区域的分布相似。值得注意的是,输入簇在SPN中普遍存在,但在FSI中不存在。我们的结果表明,由于突触输入密度较高,与S1相比,SPN与M1具有更强的功能连接。M1和S1输入在SPN上而非FSI上的聚类表明,皮质输入通过细胞类型特异性机制进行整合,并且更普遍地对纹状体中感觉运动整合的执行方式具有影响。
背外侧纹状体(DLS)是参与感觉运动整合的关键脑区,因为它受到初级运动皮层(M1)和感觉皮层(S1)的密集支配。然而,这些输入到纹状体细胞群体的数量和解剖分布尚未得到很好的描述。在本研究中,我们证明来自M1和S1的皮质纹状体投射对DLS中的棘状投射神经元(SPN)和快发放中间神经元(FSI)的支配存在差异。S1输入对SPN的支配少于M1,并且可能在SPN中形成突触簇,但在FSI中不形成。这些发现表明,感觉运动整合部分是通过皮质纹状体输入到局部纹状体微回路的突触组织差异来实现的。