Short-term dynamics of long-range corticocortical synapses revealed by selective optical stimulation

Synapses are continually regulated by their own activity. In the neocortex, direct interactions between cortical areas play a central role in cognitive function, but the dynamic regulation of these long-range corticocortical synapses by activity and their impact on a postsynaptic target neuron is unclear. Here, we use an optogenetic strategy to study the connections between mouse somatosensory and motor cortex. We found that short-term synaptic facilitation was strong in both corticocortical synapses, resulting in far more sustained responses than local intra-cortical and thalamocortical connections. This facilitation was dependent on the presynaptic calcium sensor synaptotagmin-7 and altered by several optogenetic approaches. Recordings revealed that during repetitive activation, the short-term dynamics of corticocortical synapses enhanced the excitability of layer 2/3 pyramidal neurons, increasing the probability of spiking with activity. Furthermore, the properties of the connections linking primary with secondary somatosensory cortex resemble those between somatosensory-motor areas. These results reveal a synaptic mechanism by which corticocortical projections may mediate specific changes in cellular excitability over relatively extended periods.

Brain Wiring and Supragranular-Enriched Genes Linked to Protracted Human Frontal Cortex Development

The human frontal cortex is unusually large compared with many other species. The expansion of the human frontal cortex is accompanied by both connectivity and transcriptional changes. Yet, the developmental origins generating variation in frontal cortex circuitry across species remain unresolved. Nineteen genes that encode filaments, synapse, and voltage-gated channels are especially enriched in the supragranular layers of the human cerebral cortex, which suggests enhanced corticocortical projections emerging from layer III. We identify species differences in connections with the use of diffusion MR tractography as well as gene expression in adulthood and in development to identify developmental mechanisms generating variation in frontal cortical circuitry. We demonstrate that increased expression of supragranular-enriched genes in frontal cortex layer III is concomitant with an expansion in corticocortical pathways projecting within the frontal cortex in humans relative to mice. We also demonstrate that the growth of the frontal cortex white matter and transcriptional profiles of supragranular-enriched genes are protracted in humans relative to mice. The expansion of projections emerging from the human frontal cortex arises by extending frontal cortical circuitry development. Integrating gene expression with neuroimaging level phenotypes is an effective strategy to assess deviations in developmental programs leading to species differences in connections.

Evolution of Brain Connections: Integrating Diffusion MR Tractography With Gene Expression Highlights Increased Corticocortical Projections in Primates

Diffusion MR tractography permits investigating the 3D structure of cortical pathways as interwoven paths across the entire brain. We use high-resolution scans from diffusion spectrum imaging and high angular resolution diffusion imaging to investigate the evolution of cortical pathways within the euarchontoglire (i.e., primates, rodents) lineage. More specifically, we compare cortical fiber pathways between macaques (Macaca mulatta), marmosets (Callithrix jachus), and rodents (mice, Mus musculus). We integrate these observations with comparative analyses of Neurofilament heavy polypeptide (NEFH) expression across the cortex of mice and primates. We chose these species because their phylogenetic position serves to trace the early evolutionary history of the human brain. Our comparative analysis from diffusion MR tractography, cortical white matter scaling, and NEFH expression demonstrates that the examined primates deviate from mice in possessing increased long-range cross-cortical projections, many of which course across the anterior to posterior axis of the cortex. Our study shows that integrating gene expression data with diffusion MR data is an effective approach in identifying variation in connectivity patterns between species. The expansion of corticocortical pathways and increased anterior to posterior cortical integration can be traced back to an extension of neurogenetic schedules during development in primates.

Thalamocortical Connectivity and Microstructural Changes in Congenital and Late Blindness

There is ample evidence that the occipital cortex of congenitally blind individuals processes nonvisual information. It remains a debate whether the cross-modal activation of the occipital cortex is mediated through the modulation of preexisting corticocortical projections or the reorganisation of thalamocortical connectivity. Current knowledge on this topic largely stems from anatomical studies in animal models. The aim of this study was to test whether purported changes in thalamocortical connectivity in blindness can be revealed by tractography based on diffusion-weighted magnetic resonance imaging. To assess the thalamocortical network, we used a clustering method based on the thalamic white matter projections towards predefined cortical regions. Five thalamic clusters were obtained in each group representing their cortical projections. Although we did not find differences in the thalamocortical network between congenitally blind individuals, late blind individuals, and normal sighted controls, diffusion tensor imaging (DTI) indices revealed significant microstructural changes within thalamic clusters of both blind groups. Furthermore, we find a significant decrease in fractional anisotropy (FA) in occipital and temporal thalamocortical projections in both blind groups that were not captured at the network level. This suggests that plastic microstructural changes have taken place, but not in a degree to be reflected in the tractography-based thalamocortical network.

Long-range and local circuits for top-down modulation of visual cortex processing

Top-down modulation of sensory processing allows the animal to select inputs most relevant to current tasks. We found that the cingulate (Cg) region of the mouse frontal cortex powerfully influences sensory processing in the primary visual cortex (V1) through long-range projections that activate local γ-aminobutyric acid–ergic (GABAergic) circuits. Optogenetic activation of Cg neurons enhanced V1 neuron responses and improved visual discrimination. Focal activation of Cg axons in V1 caused a response increase at the activation site but a decrease at nearby locations (center-surround modulation). Whereas somatostatin-positive GABAergic interneurons contributed preferentially to surround suppression, vasoactive intestinal peptide-positive interneurons were crucial for center facilitation. Long-range corticocortical projections thus act through local microcircuits to exert spatially specific top-down modulation of sensory processing.

Gyral window mapping of typical cortical folding using MRI

Using the NIH Pediatric MRI Data Repository for normative developmental studies, white matter depth within the gyri of the frontal, temporal, parietal, and occipital lobes, and of the left and right hemisphere was identified for 312 typically developing children and young adults (168 male and 144 female) between 4 and 23 years of age. There was no significant age difference between male and female groups overall (F 1,867 = 0.0002; p = 0.99) or per-visit (F 2,867 = 2.18; p = 0.86). There was significant dependence of gyral window upon age (F 1,6544 = 115, p < 0.0001), lobe (F 3,6544 = 229, p < 0.0001), hemisphere (F 1,6544 = 5.23, p = 0.022), age*sex (F 1,6544 = 13.8, p = 0.0002), age*lobe (F 3,6544 = 120, p = 0.0001), and age*hemisphere (F 1,6544 = 4.41, p = 0.036). Gyrification increased with age in both males and females in the frontal, temporal and parietal lobes with opposite effects observed in the occipital lobe. Relative gyral depth, as measured in this study, was significantly (p < 0.0001) inversely correlated with gyrification index. Previous studies relate gyral window measurements to the differential expression of short and long corticocortical projections. Our results therefore suggest that the pattern of corticocortical connections is malleable during the first two decades of development.