The striatum shows general topographic organization and regional differences in behavioral functions. How corticostriatal topography differs across cortical areas and cell types to support these distinct functions is unclear. This study contrasted corticostriatal projections from two layer 5 cell types, intratelencephalic (IT-type) and pyramidal tract (PT-type) neurons, using viral vectors expressing fluorescent reporters in Cre-driver mice. Corticostriatal projections from sensory and motor cortex are somatotopic, with a decreasing topographic specificity as injection sites move from sensory to motor and frontal areas. Topographic organization differs between IT-type and PT-type neurons, including injections in the same site, with IT-type neurons having higher topographic stereotypy than PT-type neurons. Furthermore, IT-type projections from interconnected cortical areas have stronger correlations in corticostriatal targeting than PT-type projections do. As predicted by a longstanding model, corticostriatal projections of interconnected cortical areas form parallel circuits in the basal ganglia.
Primary motor (M1) and primary somatosensory (S1) areas of cerebral cortex are somatotopically organized, with distinct body regions represented in adjacent areas. Though sensory and motor cortices specialize in distinct functions, corticocortical projections reciprocally connect them. Similarly, corticostriatal inputs are topographically organized. Overlaid on this pattern, however, output from any given cortical area projects broadly and overlaps with output from other areas, including topographically related ones1,2. A longstanding model of corticostriatal organization is that striatal regions integrate input from multiple cortical areas that are functionally interconnected3,4. This suggests that the striatum is organized into distinct regions2 associated with different behavioral functions5,6. While there is topographic organization, different functions of dorsolateral, dorsomedial, and ventral divisions are not rigidly spatially segregated7,8. To better understand how information from the cortex is integrated within the striatum, this study first asks whether projections from different cortical areas project to stereotyped sectors of striatum across animals by quantifying overlap and segregation between sensory, motor, and frontal projections. Stereotypy refers to the degree to which injections from a given brain location project to the same target location across different animals. As a subsequent step, these data tests whether corticocortical connectivity predicts convergence or interdigitation within the striatum.
Addressing these questions is not straightforward with conventional anatomical techniques, since the corticostriatal projection originates from two distinct excitatory neuron categories in layer 5 (L5): pyramidal tract-type (PT-type) neurons and intratelencephalic (IT-type) neurons9,10,11. PT-type neurons send projections to the thalamus, subthalamic nucleus, superior colliculus, and brainstem with collaterals in ipsilateral striatum12, but do not project to contralateral cortex nor contralateral striatum. In contrast, IT-type cells project exclusively to ipsi- and contralateral striatum and cortex, and not to other subcortical targets11. In motor areas, local circuits are hierarchically organized such that IT-type cells connect to each other and project to PT-type neurons, but PT-type neurons do not connect to IT-type cells13. Thus, information at different stages of processing is transmitted out of cortex, conveying distinct messages14.
The differences between the corticostriatal projections of these two major cell types are analyzed using stereotaxic injection of Cre-dependent reporters into sensory, motor, and frontal cortical areas of Cre-driver mice selective for IT-type and PT-type neurons. Sectioned brains are then imaged and aligned to a reference brain, the Mouse Common Coordinate Framework version 3 (CCF v3)15,16,17 to quantify axonal fluorescence in a standard coordinate system. Targeting of axonal projections in striatum and other targets of motor and sensory output is quantified to assess the topographic organization of projections. These data reveal that the topographic organization of projections differs between IT-type and PT-type neurons and between sensory and motor areas. Thus, the information cortex provides for striatal processing differs across these two cortical output channels.
A library of IT-type and PT-type corticostriatal projections
To analyze the corticostriatal projections of specific pyramidal cell types, mouse lines selectively expressing Cre in IT-type (Tlx3_PL56) and PT-type (Sim1_KJ18) neurons18 were injected with AAV expressing Cre-dependent tracers. Each mouse received injections of three different AAV vectors (GFP, td-tomato, and smFPs; Table 119) into different locations of sensory, motor and frontal cortex (Fig. 1 and Supplementary Fig. 1). A whole-brain reconstruction from tiled images20 (Supplementary Fig. 1b-e) was registered to a common reference frame using BrainMaker software (MBF Bioscience) with alignment precision of ~50–70 µm (Supplementary Fig. 1l-y). Original images were posted at: http://gerfenc.biolucida.net/link?l=Jl1tV7 (Biolucida viewer-based, free download) and http://gerfenc.biolucida.net/images/?page=images&selectionType=collection&selectionId=32 (web-based). Placing all voxels from all brains in the same reference space enabled quantitative analysis of regions of interest across different animals (Supplementary Fig. 1h-i).
As expected for IT-type neurons, injections in Tlx3_PL56 mice labeled axonal projections that bilaterally targeted cortex and striatum, but not other subcortical structures10,11 (Fig. 1e). By contrast, axonal projections in the Sim1_KJ18 line were restricted to the hemisphere ipsilateral to the injection within the cortex and striatum. Labeled neurons also projected to the thalamus, subthalamic nucleus, superior colliculus, pontine and medullary nuclei, typical of PT-type corticofugal neurons12. IT-type neurons are generally located in more superficial layer 5 than PT-type neurons, with considerable overlap. Injections in Sim1_KJ18 and Tlx3_PL56 infected a small number of L2/3 neurons. Somata of labeled pyramidal neurons at injection sites were marked in Neurolucida and their relative laminar depth plotted (Fig. 1a-d). Tlx3_PL56 and Sim1_KJ18 labeled neurons at injection sites were consistent with prior descriptions of the laminar locations of IT and PT neurons21,22. As subtypes of PT-type neurons exist, targeting either thalamus or medulla, for example, PT-type neurons of Sim1_KJ18 represent a mixture of these subpopulations since projections can be seen in a range of subcortical targets23. Similarly, IT-type neurons of Tlx3_PL56 project to multiple expected ipsi- and contralateral cortical and subcortical targets, which may be individually targeted by more finely defined subsets of IT-type neurons.
The coordinates of labeled somata for each injection in the original images were marked and transformed into the CCF reference frame (Fig. 1f-k), with the average used to determine a center of mass for the injection site (Fig. 1j). The injection site center of mass was used to cluster injection sites for Sim1_KJ18 and Tlx3_PL56 into eight clusters across sensory, motor, and frontal cortex (Fig. 1k). These corresponded to vibrissal, forelimb, and orofacial somatosensory cortices (vS1, fS1, and orfS1); vibrissal, forelimb, and lower limb motor cortices (vM1, fM1, and llM1); and frontal areas (anterior lateral motor cortex (ALM) and secondary motor cortex (M2)). Indeterminate injection sites (black) were not clustered. The names assigned to these sites correspond to the body representation determined by microstimulation mapping for motor areas24,25 and somatotopic mapping of sensory areas26,27,28. Thus, vM1 is the low-threshold region where microstimulation evokes whisker movement and also the region where vS1 axons project. This area is also called MOs in the Allen Reference Atlas15,16. M2 is the frontal region reciprocally connected to vM129, with ALM lateral to it.
A methodology was developed to quantitatively compare projections from different injections sites. Images were thresholded to eliminate 99% of background (Supplementary Fig. 1z). Three example injection sites (from Tlx3_PL56 mice in vM1, vS1, and ALM) illustrate the methodology for comparison (Fig. 2). Suprathreshold voxel intensity for ipsilateral striatum was compared on a voxel-by-voxel basis using voxels that were suprathreshold for both channels (Fig. 2a). The Pearson correlation coefficient (PCC) based on voxel intensity (AU) was used to assess the relationship within the striatum for each pair of injections (Fig. 2b). To localize where within the striatum correlations occurred, correlation was computed and plotted for each plane along the anterior/posterior axis (Fig. 2c-e). Correlation values varied dependent on both the particular injection site locations and the rostro-caudal level of the striatum. In the example shown, correlation was near zero in anterior striatum, but became well correlated for vS1 and vM1 in mid- and posterior ipsilateral striatum (black line). In contrast, correlation is negative for both vS1 and vM1 when compared to the ALM injection (yellow and blue lines, Fig. 2e, f). Correlations were noisier when measured based on small numbers of voxels (anterior and posterior poles of striatum, Fig. 2e, f). The general pattern was similar for individual pairs of injection cases (Fig. 2e; e.g., vS1 & vM1) compared to the population average across all pairs of injection cases at similar loci (Fig. 2f), but the magnitude of correlation varied considerably depending on individual M1 and S1 injection cases considered. In addition to corticostriatal terminal arborizations, there are some bright, dense fascicles specific to PT-type axons which pass through striatum without terminating. These could not easily be separated from the signal of terminal arborizations by thresholding, and thus contribute to the noise of this measurement.
The anatomical overlap of terminal arborizations, however, corresponds to shared targeting of functional synaptic output to specific single neurons. This was tested using a dual channel circuit mapping approach with conventional ChR2 and red-shifted ReaChR30 expressed in vM1 and vS1 respectively. Whole cell recordings from striatal projection neurons (SPNs) in the overlapping region of vM1 and vS1 projections revealed synaptic convergence in all neurons recorded (Supplementary Fig. 2). This confirmed that convergent axonal projections, such as those from topographically aligned regions of sensory and motor cortex, also shared functional synaptic targets.
Topography of sensory and motor corticostriatal projections
To study topography of ipsilateral corticostriatal projections, the analysis of corticostriatal correlations was extended to all eight injection clusters, which included sensory areas (vS1, fS1, and orfS1), motor areas (vM1, fM1, and llM1), and frontal areas (ALM and M2). Sensory, motor, and frontal areas were taken to represent three modalities for cortical function, with the clusters within each modality representing different somatotopic regions (whisker, forelimb, and hindlimb for example) within that modality. First, IT-type projections were quantified. Projections from different regions within the same cortical modality displayed a topographic organization along the rostral/caudal axis (Fig. 3a; adjacent locations of red, green and blue). This demonstrated the maintenance of the topographic organization within modalities in their projections to the striatum. Comparison of the projections between sensory, motor and frontal areas showed considerable overlap (Fig. 3b; mixing of red, green, and blue). Quantitative analysis reveals varying levels of corticostriatal input along the rostro-caudal axis (Fig. 3c). Somatosensory injections were biased towards more posterior sites, with maximum intensity and suprathreshold voxel numbers peaking more caudally than motor or frontal injections.
To assess corticostriatal topography, quantitative comparisons were made between injections in the same injection cluster (Fig. 3d) or across injection sites within the same modality (Fig. 3e) using the methods described (Fig. 2). Comparison of correlation coefficients between injections within the same cluster (vS1 to other vS1 injections, Fig. 3d) showed these were always positively correlated. However, there was remarkably little correlation between injection sites across clusters within the same modality (Fig. 3e-f; Supplementary Fig. 3). ALM compared to the other frontal injection site, M2, showed near-zero correlation, as did vM1-llM1, vS1-orfS1, and orfS1-fS1 comparisons. Where there was positive correlation observed in across-cluster comparisons, this was weaker than within-cluster comparisons. This suggested stereotypy in axonal projection patterns across mice. Contralateral corticostriatal projections (Supplementary Fig. 4) had grossly similar results with weaker overall correlations. Frontal areas, however, had particularly strong contralateral projections and similarly strong within-cluster correlation.
This analysis was repeated for PT-type projections grouped into the same eight clusters by injection site location (Fig. 3g-l). There were general similarities, with frontal and motor projections targeting more anterior sites and sensory projections targeting more posterior ones. In contrast to IT-type projections, PT-type projections from frontal areas had fewer suprathreshold voxels and showed reduced mean voxel intensity compared to IT-type tracing from the same region (Fig. 3i). This reduction in intensity was consistent with smaller projections and less overlap between different injection sites. In the PT-type case, there is more sensory vs. motor separation along the anterior/posterior axis (the posterior planes have more red color, Fig. 3h). In comparison, for IT-type projections, there is relatively more overlap in posterior planes (purple posterior planes in Fig. 3b). Comparisons for nearby injection cases in the same cluster (vS1 to vS1) had higher positive correlations than comparisons to injection cases in nearby clusters, such as vS1-orfS1 or vS1-fS1 (Fig. 3j-l; Supplementary Fig. 3). The correlations for all within and across group comparisons were summarized in Fig. 3l. Correlation scores were always higher for within than across group comparisons. Furthermore, PT-type projections have lower correlations than IT-type ones (Fig. 3f, l).
Topographic differences of IT-type and PT-type projections
Because these injections densely sampled sensory and motor areas, topographic specificity could be examined by comparing injections at a range of distances in the same or different cell types. Injection sites from different mice in the same location of the CCF are expected to share high correlation in their projections if connections in the rodent brain are stereotypical. Barrel cortex, for example, is sufficiently stereotyped that individual barrels are apparent in the Allen averaged registration template17. In contrast, microstimulation maps for movement show some inter-animal variability24,25. To examine the relationship between the distance between injection sites and their projections, the distance between injection site centers of mass was calculated for IT-type or PT-type injections in sensory and motor cortex. The correlation score in ipsilateral striatum was plotted against injection site offset (Fig. 4). For both sensory (blue) and motor injections (pink; Fig. 4b, d, f), the correlation score was fit with a linear regression (95% confidence interval shown). For IT-type projections, the peak correlation was higher for sensory cortical injections (~0.6) than for motor cortex (~0.4). The relationship dropped off more steeply in sensory areas (ANOCOVA, Group*X Value, p < 0.0001). Collectively, these results suggest that sensory cortical areas show stronger topographic precision than motor ones24,25,28,31,32,33. A similar relationship was apparent for PT-type projections, with higher correlations in nearby sensory injections than in motor areas (ANOCOVA, Group*X Value, p < 0.0001; N = 312, KJ18-KJ18 S1; N = 300, KJ18-KJ18 M1). Peak correlation was stronger for IT-type than PT-type projections for both sensory and motor populations.
The correlation of IT-type with PT-type injections near the same site was also studied. If these projections targeted different striatal regions, then both a reduction in the correlation as well as a reduction in the number of overlapping voxels were expected. However, the correlation versus distance relationship was similar to that of the within PT-type injection comparisons (Fig. 4f) while the number of overlapping voxels was intermediate to IT–IT and PT–PT comparisons (Fig. 4e). Corticostriatal projections of both types tended to target the same striatal regions for a given cortical injection site, as the center of mass of corticostriatal fluorescence was generally found in the same portions of striatum (Fig. 5). Differences in these correlations could thus not be attributed to IT-type and PT-type neurons from the same cortical area targeting largely distinct striatal regions.
The departure from perfect correlation between projections from nearly overlapping injection sites could result from differences in the injection size (including number of infected cells and scatter at the injection site), inter-animal variability, or noise in image acquisition. Thus, whether different degrees of injection site scatter resulted in less correlation was tested. Injection site scatter was measured as the standard deviation for each infected soma from the injection site center of mass in a given injection. This was used to divide injections into two categories: those with scatter higher or lower than the mean. Correlation of ipsilateral striatal projections for low and high scatter groups was compared (Supplementary Fig. 5). Two populations were nearly indistinguishable, suggesting that injection size was not a major contributor to differences in correlations.
One model of corticostriatal organization suggests that striatal regions integrate input from multiple interconnected cortical areas4. This predicts that reciprocally connected regions of sensory and motor cortex would have elevated correlation in their striatal projections. Thus, a measure of corticocortical correlation was used to assess how well two given injection cases were reciprocally connected, and the correlation of their corticostriatal projections was used as a measure of integration in striatum. Pairwise comparisons between motor and sensory injections were thus examined for co-correlation. To assess the degree of corticocortical correlation, overlap of S1-originating axons with labeled neurons at M1 injection sites was determined (and vice-versa for M1-originating axons). The M1 and S1 injection sites were defined in the CCF using coordinates that encompassed all labeled somata at the motor or sensory injection site, and included all voxels from pia to white matter. The correlation between a pair of M1 and S1 injections was then determined in this cortical volume, using the methods described in Fig. 2. Scatterplots compare the corticocortical correlation to the corticostriatal correlation for the same pair of injection cases (green and teal arrows, Fig. 6d, e). Each point represents the comparison of a single pair of injection cases. Red points specifically highlight comparisons between sensory and motor injections. Black points label pairwise comparisons between frontal areas and either motor (Fig. 6d) or sensory cortex (Fig. 6e). For IT-type projections, there was a positive relationship for striatal comparisons to M1 and S1 injection sites (Fig. 6d, e; R2 = 0.3640 for striatal correlation vs M1 injection site correlation; R2 = 0.3055 for S1 injection site correlation). In contrast, PT-type projections did not show this strong relationship (Fig. 6h, i and Supplementary Fig. 6; R2 = 0.0038 for striatal correlation vs M1 injection site correlation; R2 = 0.1219 for S1 injection site correlation). Because IT-type corticostriatal projections generally project to a greater area in striatum (Figs 3, 4), it is possible the increased co-correlation resulted from IT-type projection overlap in a focal region not innervated by PT-type neurons. Thus, the relationship between anterior/posterior subsets of the striatum with corticocortical connectivity (measured as before) was assessed by examining the co-correlation of cortical and striatal connectivity along 250 µm striatal segments. The co-correlation is determined by the correlation of two correlation coefficients (the graphs of Figs 6d, e and 5h, I, computed for anterior/posterior subsets of striatal voxels). This revealed a long plateau of high co-correlation across the rostro-caudal extent of striatum (Fig. 6j) for IT-type but not PT-type projections. The enhanced co-correlation for IT-type projects did not result from a single focal region, but was spread across the extent of the corticostriatal projection. Thus, interconnected cortical areas shared projection targets in basal ganglia, but this relationship was stronger for the IT-type subset of corticostriatal projections.
Arborization and targeting of single IT-type and PT-type axons
Mean projections were based on ~600–900 neurons per injection (IT-type injections 906.9 ± 71.7, PT-type injections 612.1 ± 44.7, mean ± sd). Examination of axonal arbors of single neurons shed light on how variable the projections of each population of pyramidal neurons might be. In the MouseLight project34, single axons of IT- and PT-type cells in primary and secondary motor cortex were imaged and registered to the Allen Reference Atlas. Although a limited number of total neurons were available, individual axons extended certain aspects of these findings. IT-type and PT-type neurons in the same area shared a similar corticostriatal topography, though IT-type arbors were more extensive and PT-type arbors were more focal (Fig. 7a-c). Comparison of multiple primary motor cortex (M1) projections confirmed that larger IT-type arbors have more overlap, while more focal PT-type projections were less likely to overlap. From the same area, PT-type axons innervated a subset of the region innervated by IT-type axons (Fig. 7d–f). The overall pattern of IT-type projections differed between M1 and M2 (Fig. 7g–i): M1 axonal projections targeted more focal areas, while, in contrast, individual M2 axons projected more broadly within the striatum, resulting in considerable overlap and only a rough topographic organization. M2 projections were also stronger to contralateral striatum. Individual IT-type neurons in M1 and M2 showed considerable heterogeneity in terms of bilateral projections, with some neurons projecting axons primarily ipsilaterally, some contralaterally, and some bilaterally (cf. IT-type gold vs. red). Considerable variation between individual IT- and PT-type neurons suggested that further subclassification of these cell types is needed.
Striatum is loosely organized in topographic areas
IT-type and PT-type projection correlations were used to construct hierarchical relationships between cortical injection sites based on the projections to ipsilateral striatum. Pairwise correlation scores for IT-type outputs were used to construct a dendrogram using Euclidean distance between correlations as the distance measure. Generally, nearby injection sites showed the greatest affinity (Fig. 8a-c). At higher hierarchical levels, most fS1 and vS1 injections clustered together. Motor injections in vM1, fM1, llM1, and M2 also clustered together. Unexpectedly, orfS1 clustered with ALM, suggesting an affinity between lateral sensory and frontal areas in their projections to ipsilateral striatum. Of interest, this affinity also recurred in a similar analysis of corticocortical correlations (Supplementary Fig. 7). In contrast to the IT-type results, using the same methodology to examine PT-type corticostriatal outputs, sensory inputs clustered together, separately from motor and frontal inputs (Fig. 8d-f).
Differences in input contribute to differences in striatal function. Since corticostriatal afferents form a major excitatory input, differences in sensory, motor, and frontal corticostriatal projections could identify functionally distinct striatal regions. Average normalized projection patterns were determined from eight injection clusters for two mouse lines. The normalized projection strength was used to assign ipsilateral striatal voxels into clusters using k-means clustering. Five clusters were found based on the peak silhouette value. These were presented in coronal section for the ipsilateral striatum using five colors (Fig. 9a). The fraction of output to each of the clusters is shown for IT-type and PT-type projections (Fig. 9b, c). One cluster (blue) covered the anterior, medial, and posterior edges of the striatum, which were predominantly regions receiving poor output from sensorimotor cortex. The dorsolateral sector included (a) an anterior core region (green) that received substantial M2 and primary motor output, (b) an anterior dorsolateral region (olive) that received strong motor output and some sensory output, and (c) a posterior dorsolateral region (red) that received strong sensory output and some motor output. The ventral and posterior domain received input from ALM and orfS1. This analysis was repeated for IT-type projections alone and PT-type projections alone (Supplementary Fig. 8). Clustering based on IT-type input alone resulted in four clusters, with the anterior and posterior dorsolateral regions that were separable based on both projections combined into a single cluster when PT-type data were excluded. This shift highlighted a difference in the IT-type and PT-type projections: the primary motor projections favored the anterior (olive) dorsolateral cluster, while the primary sensory projections favored the posterior (red) dorsolateral cluster. This difference was more pronounced for PT-type than for IT-type. Thus, differences in PT-type projections identified putative functionally distinct regions of striatum. That these regions were divided by PT-type sensory and motor outputs is also consistent with the earlier dendrogram (Fig. 8). The clustering of IT-type outputs to contralateral striatum was similar to ipsilateral striatum, but not as well defined. Three clusters were sufficient to describe contralateral projections (Supplementary Fig. 8). Consistent with this, the overall correlation coefficients were reduced for these projections (Supplementary Fig. 4). This implied a reduction in the topographic specificity of contralateral striatal projections.
How do the corticostriatal projections of PT-type and IT-type neurons differ? The current data show that corticostriatal projections of interconnected cortical areas replicate their corticocortical connectivity by projecting to shared targets in the striatum, as predicted2,4 (Fig. 6). However, this model2,4 did not distinguish between cell-type-specific projections. Discriminating between IT-type and PT-type afferents revealed this model best describes IT-type projections. Differences in the corticostriatal topography of projections for specific cell types within a cortical region had not previously been predicted. The basis for this difference is not that the center of mass of corticostriatal fluorescence differs (Fig. 5). Instead, within nearby cortical sites, there is greater heterogeneity in the PT-type projection between animals, as well as between axonal projections of single cells (Fig. 7). Thus, PT-type output is more focal, but less stereotyped in its targeting, compared to IT-type output. Pairwise comparison of PT-type and IT-type injection cases confirms this (Figs 3, 4), as does single-axon data (Fig. 7). These differences have been difficult to appreciate with conventional tracing techniques, though overlapping projections in subcortical targets including thalamus have been effective as a measure of topographic alignment between cortical sites1. Fine afferents may be missed in the corticostriatal projection in the Golgi method35 and tracers do not distinguish between cell types2,26. However, single axon fills in rat have previously demonstrated differences in the degree of corticostriatal terminal arborization between these two cell types10. Thus, cell type-specific lines are advantageous for anatomical tracing since the long-range projections of different cell types are organized differently16,36.
The relative importance of IT-type and PT-type corticostriatal projections is unclear. Both cell types are significant in rodents, as seen here. PT-type collaterals are also present in primates37, but some studies argue are less prominent14,38. These neuronal subtypes receive distinct inputs11 and convey different classes of information to descending circuits14. Thus, these differences may contribute to functional specialization within the striatum. These quantitative assessments of correlation for corticostriatal projections would be difficult to achieve with lower resolution alignment (>100 µm voxels) or the scoring of axons as present or absent (reducing the bit depth of images), which may limit similar studies2,26,39. Inclusion of other subtypes of projections, such as L2/3 pyramidal neurons or thalamic inputs39, or further subdividing IT-type neurons (as is possible with MouseLight) may reveal more nuanced structure within the corticostriatal projection.
Addressing the functional significance of these anatomical differences is difficult. Focal PT-type output to a smaller subset of striatal neurons might be useful for activation of a targeted subset of the basal ganglia circuitry associated with the specific set of musculature targeted by the brainstem and spinal networks activated by the descending axon of the same PT-type cell. In contrast, IT-type outputs might represent a broader signal to initiate movement or govern its vigor. Thus, the enhanced overlap of IT-type projections from corresponding motor and sensory topographic areas might be more important for more general signals to coordinate movement as opposed to specific signals related to movement initiation of a specific muscle. However, this does not yet explain how each pathway differentially contributes to plasticity during skill acquisition40.
The difference in correlation of corticostriatal projections as a function of injection site offset between pairs of nearby primary motor or pairs of primary somatosensory injection cases is remarkable (Fig. 4b, d). In comparing IT-type injections in S1 and M1, the highest correlations are found for nearby injections in S1 (Fig. 4). The steep drop in correlation with increasing distance between injection sites is consistent with a greater topographic specificity in primary somatosensory areas. This is paralleled by functional data, where specific areas of S1 are highly specific for certain body regions such as barrel cortex, where individual barrels are specific for a single whisker27. In contrast, microstimulation data suggest that motor representations, while topographically organized, are also generally intermingled24,25,28,32,33,41,42. The basis of these topographic differences may derive from the fact that somatosensory cortical areas have a clearly defined input for a given cortical column, such as the primary thalamocortical afferent to layer 4, representing touch of a single finger or whisker43. In contrast, primary motor areas have less spatially restricted thalamic44 and cortical29 inputs. The neurons in these areas may represent a more diverse range of phenomena45, ranging from muscles46,47 to movements48 and behaviors49, where body representation alone is not sufficient. It is worth noting that the decrease of correlation with injection site offset is relatively linear instead of stepwise, though smaller steps in the noise are possible. This is consistent with a gradual shift in topographic representation of body regions in striatum instead of discrete segments dedicated exclusively to a single region2.
This relationship is also true between sensory and motor injections labeling PT-type neurons, but the overall level of correlation is lower. This was unexpected. These projections, as collaterals of output targeting subcortical targets, were expected to be more precise. The higher correlation of IT-type projections is not due to targeting of a specialized IT-specific striatal region or a substantial offset in the projection zones of the two cell types, as the center of mass of corticostriatal fluorescence for PT- and IT-type projections is similar across the anterior/posterior extent of the striatum (Fig. 5). Instead, quantification of PT-type collaterals showed that these projections have fewer suprathreshold voxels and thus are more spatially limited (Figs 3, 4). Individual axon reconstructions, such as MouseLight data, show that striatal axons of IT neurons are more highly branched than those of PT neurons10. Therefore, individual PT-type terminals are more focal (Fig. 7). But these PT-type terminals also show less spatial overlap and higher variability for nearby injection site cases (Fig. 4) or between nearby cells (Fig. 7). This correlation is not simply due to a reduction in the volume of overlap, as comparisons between PT- and IT-type injections in nearby sites showed an increase in overlap volume, but relatively low correlations comparable to PT–PT correlations for the same injection site offset (Fig. 4). Thus, peak correlation is not simply driven by overlap volume.
Although there is strong evidence from primates4 and rodents50 for convergence of corticostriatal afferents from associated cortical areas, some data51 suggests S1 and M1 projections are largely non-overlapping. This result may differ from those presented here if the topographic alignment of the two sites is imprecise (Figs 4, 6). The dual channel recordings presented here (Supplementary Fig. 2) show synaptic convergence of S1 and M1 outputs for all SPNs recorded, demonstrating that integration of topographically aligned sensory and motor signals is a relatively frequent characteristic of striatal neurons.
Contralateral corticostriatal projections of IT-type neurons show reduced correlations compared to ipsilateral axons (Supplementary Fig. 4). Thus, the precision of axonal targeting varies across different collaterals of the same cell type. Since it would be possible to use the same molecular and activity-dependent cues to achieve the same precision in ipsi- and contralateral connections, it will be interesting to learn the functional import of generating a contralateral projection with less spatial precision than the ipsilateral one. On the one hand, longer-range contralateral projections might lose some topographic precision, but how does the animal benefit from a less precise contralateral projection? Such inputs would seemingly degrade the precision of input to contralateral SPNs.
Notably, overall projection density differs across IT-type and PT-type neurons moving from frontal to motor and sensory areas by number of supratheshold voxels (Fig. 5) and mean voxel intensity (Fig. 3c, i). In IT-type injections, frontal projections provided the densest striatal afferents. In contrast, for PT-type injections, frontal injections were by contrast the weakest (Figs 3, 4). Thus, PT-type projections contribute to a relatively higher proportion of the total corticostriatal output from sensory areas. This difference is useful in subdividing the striatum into sectors, where including both PT- and IT-type projection data helps differentiate anterior and posterior dorsolateral striatal areas specialized for motor and sensory input, respectively (Fig. 9, clusters 3 and 5) which merge when IT-type only output is considered (Supplementary Fig. 8a). The precision of the striatal subdivisions presented is stronger in dorsolateral areas than ventrally, where corticostriatal afferents originate outside sensorimotor areas and were not sampled. However, even with dense sampling, it was not straightforward to identify clusters exclusive to specific body parts without overlap.
Several sources may limit the ability to measure stereotypy of corticostriatal projections. Relatively compact versus scattered injection sites did not show a large variation in corticostriatal correlations, suggesting that injection site size did not play a major role in variation between injections. Thus, animal-to-animal variation instead of injection variability may play a larger role in limiting the peak correlation. Other limitations include the spatial resolution of the alignment (~50–70 µm) and voxel size, which could reduce correlations by spatial averaging. Using higher resolution aligned images (10 × 10 × 10 µm voxels) did not alter the linkages between injection sites (data not shown). That peak correlations are close to 0.6 suggests that animal-to-animal variation sets an upper limit on comparisons across brains. That peak correlations are not closer to 1.0 quantified the substantial inter-case variability and underscores the relevance of studying injections across cases in different animals instead of using a single injection case to assess typical projection targets in striatum.
Although frontal areas, such as ALM and M2, might be organized differently than sensory and primary motor cortex, it was interesting that IT-type projections from lateral regions of frontal cortex (ALM) projected to striatum similarly to those originating from orofacial regions of S1 anterior and lateral to barrel cortex. Of note, the corticocortical collaterals of ALM also projected posteriorly toward lateral regions of motor and somatosensory cortex. This was reciprocated by projections from orfS1 to ALM. Thus, ALM’s corticocortical connectivity suggested a basis for corticostriatal overlap with orfS1 projections. Coincidentally, ALM has been identified as a low-threshold region for evoking tongue movement in rodents24,52,53. Based on this connectivity pattern, ALM and orfS1 are connected in a manner reminiscent of primary motor and sensory regions, as previously suggested26. ALM has also been implicated in more traditional frontal cortex functions such as motor planning in mice54,55.
A comprehensive study of differences in cortical cell type (IT or PT type) output to distinct striatal populations was not possible from all cortical areas to the range of striatal neuron populations, including direct and indirect SPNs as well as striatal interneuron populations. Targeting of afferents to distinct striatal compartments such as patch and matrix may also differ between different cortical areas, though average sensorimotor populations target both patch and matrix neurons in similar proportions56. Afferents from both IT- and PT-type cells form connections to direct and indirect-pathway SPNs57. It not yet possible to evaluate, however, whether there is a bias in targeting from either PT- or IT-type output, as has been proposed58,59, because of quantitative limitations in circuit mapping methods. Retrograde tracing with transgenic rabies suggests that sensory and motor inputs preferentially excite direct and indirect-pathway SPNs, respectively60, suggesting specific postsynaptic targeting of afferents is possible in striatum. Physiological data (Supplementary Fig. 2) show that motor and sensory corticostriatal afferents converged on single SPNs (Supplementary Fig. 2), but did not quantitatively distinguish between the cell types targeted.
Layer-specific Cre-driver lines such as Tlx3_PL56 and Sim1_KJ18 lines may not collectively label all L5 pyramidal neurons. For example, in the L5 mouse line Rbp4_KL100, some IT-type and PT-type neurons are labeled, but the overall labeling density leaves many cells of both classes unlabeled18. The density of PT-type and IT-type neurons in Sim1_KJ18 and Tlx3_PL56 lines varies over cortical areas, which suggests that some neurons may be missed in different regions. There may be underappreciated heterogeneity within these two L5 populations, such as different subtypes of IT neurons for different targets61. Furthermore, in ALM injections of frontal cortex in Sim1_KJ18 mice, some contralateral axonal projections are present. In other areas, such as midline cortical areas where lamination is less pronounced, transgenic reporters for these lines suggest changes in Cre expression, resulting in reduced Tlx3_PL56 and Sim1_KJ18 labeling18. Thus, use of transgenic approaches to target specific cell types is limited to the brain regions where these cell types are well characterized.
The corticostriatal projection formed by two populations of L5 pyramidal neurons conveys distinct functional information with distinct striatal targeting. IT-type neurons in sensory and motor areas target topographically organized domains of striatum and also overlap substantially with other cortical areas with which they are reciprocally connected. PT-type neurons, in contrast, show less overlap with reciprocally connected cortical areas. This difference suggests that the measured degree of topographic organization depends in part on the cell type considered. As these cell types convey distinct information to striatum, it remains to be determined what purpose this differential targeting serves.
All breeding, surgical, and experimental procedures conformed to National Institutes of Health guidelines for mice and were approved by the Institutional Animal Care and Use Committees of University of Pittsburgh and Janelia Research Campus. Mice from four GENSAT BAC Cre-recombinase driver lines (Sepw1_NP39, N = 7; Tlx3_PL56, N = 33; Sim1_KJ18, N = 22; and Ntsr1_GN220, N = 5)18 were used to trace the projections of four populations of cortical pyramidal neurons. Mice of both sexes were injected at postnatal day P37.0 ± 1.7 (mean ± se) and sacrificed after 2–3 weeks of expression. All stereotaxic injections targeted the same hemisphere. Injection sites covered a range of topographic locations in primary somatosensory cortex and corresponding areas of motor and frontal cortex24,25,26. 30 nL per injection site of AAV-flex-XFPs were injected using a custom positive displacement injector via a pulled borosilicate glass micropipette29. The generic AAV-flex-XFP refers to several tracing viruses used, including AAV2/1-CAG-flex-EGFP, AAV2/1-CAG-flex-tdTomato, and the GFP- and mRuby2-based spaghetti monster fluorescent proteins (smFPs) smFP-FLAG, smFP-Myc, smFP-V5, smFP-HA, Ruby2-FLAG, and Ruby2-OLLAS (Table 1)19. Injections were made into cortex (at 300–1100 µm depth). For injections into L5 and L6, virus was injected at two depths. Laminar specificity was achieved by Cre-recombinase instead of injection depth. Typically, three sites were injected per mouse. In some cases, fewer channels were quantified if expression was not usable in a given channel due to weak expression or marked spread of the virus away from the injection site.
Histology, staining, and imaging
Mice were transcardially perfused with 4% paraformaldehyde in phosphate-buffered saline and postfixed overnight. Brains were then transferred to 20% sucrose in PBS for storage. Brains were sectioned at 80 µm and signal was immunoamplified. 1:100 dilution of Neurotrace Blue was used as a structural marker20. Sections were then imaged using Neurolucida (v2017, MBF Bioscience, Williston, VT) on a Zeiss Axioimager (Zeiss, Oberkochen, Germany) equipped with 10x objective, Ludl motorized stage and a Hamamatsu Orca Flash 4.0 camera (Hamamatsu, Hamamatsu City, Japan). Each section was comprised of an average of ~100–200 image stacks collected in 10 µm steps. A single 3D image was first generated then a deeper field-of-view was achieved by collapsing images to a single plane using a DeepFocus algorithm18,20 (Supplementary Fig. 1b-e) implemented in Neurolucida. Original images are available at: http://gerfenc.biolucida.net/link?l=Jl1tV7
Whole-brain reconstruction, annotation, and registration
Tiled images were aligned to a standard coordinate system using BrainMaker software (MBF Bioscience, Williston, VT). Resulting serially reconstructed brains contained 10 µm isotropic voxels (782 × 1086 × 1242) and were registered to the annotated Allen Mouse Common Coordinate Framework (CCF), Version 3 (http://connectivity.brain-map.org)15,16,17. All brains were registered to this framework using Neurotrace Blue images as the structural marker and a two-stage registration process. The first stage constructed an average reference space that provides a representation of the average appearance of brains that have undergone histological sectioning, mounting, and staining specific to this study and in the same image channel (i.e., Neurotrace Blue). Registration of individual brains to this average reference space was found to be more robust than direct multimodal registration to the Allen CCF reference image.
The average reference image was constructed from 78 individual 3D brains in a manner similar to the Allen CCF, which incorporates 1675 individual brains with cytoarchitecture visualized with 2-photon auto-fluorescence17. In this study, the counterstain (Neurotrace Blue) channel for each individual brain was registered to a reference template, initialized as one of the individual brains resampled with a uniform voxel spacing. Multiple resolution registration optimized the 12 parameters of a 3D affine transform to minimize a normalized correlation metric between each brain and the template image. The reference template was then updated by resampling all individual brains with their respective affine transforms and computing a voxel-wise weighted average. Voxels that received a small number of contributions were discarded to correct for some tissue damage present in individual brains. A second pass registered each individual brain to the new template, updating the individual transforms. This process repeated until the template image stabilized.
The second stage involved registering the average reference image to the Allen CCF. 300 unique landmark points were identified in the average reference image and corresponding points in the Allen CCF 2-photon reference image. The positions of the landmark correspondences were used to construct a nonlinear transform that models deformation of a uniform mesh grid with B-splines. This transform was used to resample the Allen CCF annotation volume in the average reference image using nearest neighbor interpolation. The result, an average reference image and its spatially aligned annotation volume, constitutes the average reference atlas. The counterstain channels of individual brains in this study were registered with the average reference space by adjusting parameters of a 3D affine and 3D nonlinear B-spline transform to minimize a normalized correlation metric. Some but not all individual brains contributed to the average reference space. Measurement of alignment precision showed this was accurate to ~50–70 µm (Supplementary Fig. 1l-y). Comparable studies use alignment methodologies with less precision (~100 µm), larger voxels (100–150 µm per side)39 or images reduced from 8-bit to 2-bit (“dense/strong”, “moderate”, “diffuse/light”, etc.)2,26.
The recovered transform was used to map the locations of fluorescence and cell soma locations detected on fluorescent tracer channels. For quantification of injection site location, tiled images were imported into Neurolucida software (MBF Bioscience, Williston, VT) and soma locations were annotated using automated object detection with manual supervision. Nearest neighbor interpolation of the average reference space volume at the mapped positions provided the anatomical region assignment for each cell. Coordinates of the CCF for structures of interest (such as striatum) were used to identify voxels for quantification. These were divided into left and right hemispheres to distinguish between structures ipsilateral and contralateral to the injection site.
Aligned brain images were downsampled to 50 µm isotropic voxels (156 × 217 × 248) using custom routines in FIJI software62. The annotated Allen Mouse CCF was also used at 10 µm and downsampled to 50 µm. The annotation was used to assign voxels to a given brain region (ipsilateral or contralateral striatum, for example). Both 10 µm and 50 µm images were converted from tifs into.mat files in Matlab (Mathworks, Natick, MA) for analysis with custom routines. Soma locations were similarly imported to Matlab.
Individual neurons are reconstructed using fast volumetric serial two-photon (STP) tomography34 with voxels of 0.1 µm3, scanning a cleared mouse brain in ~1 week. Low numbers of individual neurons were labeled using high titer ( > 10E12 GC/ml) AAV 2/1 CAG-Flex-eGFP with dilute (1:45,000) AAV 2/1 Syn-iCre injected into cortex. Images were tiled in smaller 3D stacks (tiles in XY) and the sample translated using a mechanical stage. Scanning in the Z-direction was achieved with a piezoelectric to move the objective. Tissue was sectioned with a custom Leica 1200 S integrated with the imaging system. Both green and red channels are acquired. Neurons were manually reconstructed. Images were registered using custom Matlab scripts. Tiles were resampled into a common coordinate space with affine transforms determined during registration.
The data that support the findings of this study are available from the corresponding authors upon request. Aligned images in 10 and 50 μm voxels for all brains, cell soma locations, and the corresponding masks used to identify brain regions (striatum, for example) are available on request. Custom Matlab code for data analysis is available on request. Original images of whole brains are freely available online at: http://gerfenc.biolucida.net/link?l=Jl1tV7.
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The authors thank David Robbe, Taehyeon Kim, Sandra Okoro, YingXin Zhang-Hooks, Eric Yttri, and Peter Strick for insightful comments on the figures and manuscript. We thank Karel Svoboda, members of the Svoboda lab, and members of Janelia’s Vivarium staff for resources and discussion during the initiation this project. The authors thank Jack Glaser, Paul Angstman, Nate O’Connor, Sue Tappan, Mike Fay and Scott Gerfen at MBF Bioscience for the collaboration to develop and use the BrainMaker software. This work was supported by a NARSAD Young Investigator Award to BMH and by NINDS/NIH (R01 NS103993).
B.S.E. is an employee of MBF Bioscience, which produces Neurolucida and BrainMaker software. The remaining authors declare no competing interests.
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Hooks, B.M., Papale, A.E., Paletzki, R.F. et al. Topographic precision in sensory and motor corticostriatal projections varies across cell type and cortical area. Nat Commun 9, 3549 (2018). https://doi.org/10.1038/s41467-018-05780-7
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