Toshiki Tani

Orientation-restricted continuous visual exposure induces marked reorganization of orientation maps in early life

To elucidate the effect of visual experience on the development of orientation maps, we conducted intrinsic signal optical imaging of the visual cortex of kittens that were continuously exposed to a single orientation through cylindrical-lens-fitted goggles under a freely moving condition starting at post-natal week 3. We observed a rapid reorganization of orientation maps, characterized by extensive representation of exposed orientations with reduced responsiveness to unexposed orientations. The over-representation of exposed orientation was marked for 1-2 weeks of goggle rearing. A longer period of goggle rearing, however, decreased the degree of over-representation, which still remained at a remarkable level. Dark rearing episodes daily interleaved between single orientation exposures moderated the over-representation effect. Unit recording from goggle-reared kittens showed preferred orientations consistent with optical imaging. Using c-Fos immunoreactivity mapping, we showed that the number of neurons strongly responding to the exposed orientation was 3 times larger in a goggle-reared cat than the number of neurons responding to the vertical orientation in a normal cat. Taken together, these results suggest that the reorganization of orientation maps was caused by the expansion of domains maximally responding to exposed orientation as well as the strong reduction of responses to unexposed orientations.

A postnatal critical period for orientation plasticity in the cat visual cortex.

Orientation selectivity of primary visual cortical neurons is an important requisite for shape perception. Although numerous studies have been previously devoted to a question of how orientation selectivity is established and elaborated in early life, how the susceptibility of orientation plasticity to visual experience changes in time remains unclear. In the present study, we showed a postnatal sensitive period profile for the modifiability of orientation selectivity in the visual cortex of kittens reared with head-mounted goggles for stable single-orientation exposure. When goggle rearing (GR) started at P16-P30, 2 weeks of GR induced a marked over-representation of the exposed orientation, and 2 more weeks of GR consolidated the altered orientation maps. GR that started later than P50, in turn, induced the under-representation of the exposed orientation. Orientation plasticity in the most sensitive period was markedly suppressed by cortical infusion of NMDAR antagonist. The present study reveals that the plasticity and consolidation of orientation selectivity in an early life are dynamically regulated in an experience-dependent manner.

Parallel development of orientation maps and spatial frequency selectivity in cat visual cortex

In an early stage of the postnatal development of cats, orientation maps mature and spatial frequency selectivity is consolidated. To investigate the time course of orientation map maturation associated with the consolidation of spatial frequency selectivity, we performed optical imaging of intrinsic signals in areas 17 and 18 of cats under the stimulation of drifting square‐wave gratings with different orientations and spatial frequencies. First, orientation maps for lower spatial frequencies emerged in the entire part of the lateral gyrus, which includes areas 17 and 18, and then these orientation maps in the posterior part of the lateral gyrus disappeared as orientation maps for higher spatial frequencies matured. Independent of age, an anteroposterior gradient of response strengths from lower to higher spatial frequencies was observed. This indicates that the regional distribution of spatial frequencies is innately determined. The size of iso‐orientation domains tended to decrease as the stimulus spatial frequency increased at every age examined. In contrast, orientation representation bias changed with age. In cats younger than 3 months, the cardinal (vertical and horizontal) orientations were represented predominantly over the oblique orientations. However, in young adult cats from 3 to 9 months old, the representation bias switched to predominantly oblique orientations. These age‐dependent changes in the orientation representation bias imply that orientation maps continue to elaborate within postnatal 1 year with the consolidation of spatial frequency selectivity. We conclude that both intrinsic and mutual factors lead to the development of orientation maps and spatial frequency selectivity.

Chronically mountable goggles for persistent exposure to single orientation.

To examine the effect of experience on the developmental plasticity of functional maps in the visual cortex, we need to establish a method for a stable visual experience manipulation under the freely moving condition. For this purpose, we fabricated goggles that are chronically mounted stably on the animals head, but easy to replace according to the animals growth. Here we report the design of the goggles and the method of mounting them on the head of animals. By this method, combined with the intrinsic signal optical imaging technique, we were able to observe a rapid and robust reorganization of orientation maps.

Single Axon Branching Analysis in Rat Thalamocortical Projection from the Anteroventral Thalamus to the Granular Retrosplenial Cortex

The granular retrosplenial cortex (GRS) in the rat has a distinct microcolumn-type structure. The apical tufts of dendritic bundles at layer I, which are formed by layer II neurons, co-localize with patches of thalamic terminations from anteroventral (AV) thalamic nucleus. To further understand this microcolumn-type structure in the GRS, one of remaining questions is whether this structure extends into other layers, such as layers III/IV. Other than layer I, previous tracer injection study showed that AV thalamic nucleus also projects to layer III/IV in the GRS. In this study, we examined the morphology of branches in the GRS from the AV thalamus in single axon branch resolution in order to determine whether AV axon branches in layer III/IV are branches of axons with extensive branch in layer I, and, if so, whether the extent of these arborizations in layer III/IV vertically matches with that in layer I. For this purpose, we used a small volume injection of biotinylated dextran-amine into the AV thalamus and reconstructing labeled single axon branches in the GRS. We found that the AV axons consisted of heterogeneous branching types. Type 1 had extensive arborization occurring only in layer Ia. Type 2 had additional branches in III/IV. Types 1 and 2 had extensive ramifications in layer Ia, with lateral extensions within the previously reported extensions of tufts from single dendritic bundles (i.e., 30–200 μm; mean 78 μm). In type 2 branches, axon arborizations in layer III/IV were just below to layer Ia ramifications, but much wider (148–533 μm: mean, 341 μm) than that in layer Ia axon branches and dendritic bundles, suggesting that layer-specific information transmission spacing existed even from the same single axons from the AV to the GRS. Thus, microcolumn-type structure in the upper layer of the GRS was not strictly continuous from layer I to layer IV. How each layer and its components interact each other in different spatial scale should be solved future.

Voltage-sensitive-dye imaging of microstimulation-evoked neural activity through intracortical horizontal and callosal connections in cat visual cortex

Recently, intrinsic signal optical imaging has been widely used as a routine procedure for visualizing cortical functional maps. We do not, however, have a well-established imaging method for visualizing cortical functional connectivity indicating spatio-temporal patterns of activity propagation in the cerebral cortex. In the present study, we developed a novel experimental setup for investigating the propagation of neural activities combining the intracortical microstimulation (ICMS) technique with voltage sensitive dye (VSD) imaging, and demonstrated the feasibility of this setup applying to the measurement of time-dependent intra- and inter-hemispheric spread of ICMS-evoked excitation in the cat visual cortices, areas 17 and 18. A microelectrode array for the ICMS was inserted with a specially designed easy-to-detach electrode holder around the 17/18 transition zones (TZs), where the left and right hemispheres were interconnected via the corpus callosum. The microelectrode array was stably anchored in agarose without any holder, which enabled us to visualize evoked activities even in the vicinity of penetration sites as well as in a wide recording region that covered a part of both hemispheres. The VSD imaging could successfully visualize ICMS-evoked excitation and subsequent propagation in the visual cortices contralateral as well as ipsilateral to the ICMS. Using the orientation maps as positional references, we showed that the activity propagation patterns were consistent with previously reported anatomical patterns of intracortical and interhemispheric connections. This finding indicates that our experimental system can serve for the investigation of cortical functional connectivity.

Functional columns in superior temporal sulcus areas of the common marmoset.

Cortical areas in the superior temporal sulcus (STS) of primates have been recognized as a part of the ‘social brain’. In particular, biological motion stimuli elicit neuronal responses in the STS, indicating their roles in the ability to understand others’ actions. However, the spatial organization of functionally identified STS cells is not well understood because it is difficult to identify the precise locations of cells in sulcal regions. Here, using a small New World monkey, the common marmoset (Callithrix jacchus) that has a lissencephalic brain, we investigated the spatial organization of the cells responsive to other’s actions in STS. The neural responses to movies showing several types of other’s actions were recorded with multicontact linear-array electrodes that had four shanks (0.4 mm spacing), with eight electrode contacts (0.2 mm spacing) for each shank. The four shanks were penetrated perpendicular to the cortical surface. We found that STS cells significantly responded to other’s goal-directed actions, such as when an actor marmoset was reaching for and grasping a piece of food. The response profiles to the movies were more similar between the vertically positioned electrodes than horizontally positioned electrodes when the distances between electrodes were matched. This indicates that there are functional columns in the higher-order visual areas in STS of the common marmoset.

Sparse coding of harmonic vocalization in monkey auditory cortex

One of the potential foundations for the perception of harmony is the neurons in the primary auditory cortex (A1) that specifically respond to harmonically related frequencies, whose underlying organizing principles are yet unclear. We hypothesize that such harmony-related responses result from adapting to natural harmonic sounds by using sparse coding, a computational model that originally related natural image statistics to the neural properties of the primary visual cortex (V1). Our previous work has shown that a set of harmonic responses found in A1 of marmoset monkeys can emerge by sparse coding of highly harmonic sounds; however, the work was only preliminary because the specific sounds we used were unfamiliar to monkeys. In the present study, we recorded voices of marmosets, and showed that the same model applied to the conspecific vocalizations can reproduce the harmony-related responses. This result more directly supports the hypothesis that A1 adapts to natural sounds, in particular voices comprising harmonic overtones, under the principle of sparse coding.

Theoretical and experimental studies of relationship between pinwheel centers and ocular dominance columns in the visual cortex

In the visual cortex, pinwheel centers, which appear as point singularities in orientation maps, are likely to be found at the centers of ocular dominance columns in normal cats and monkeys. To elucidate the mechanism underlying the geometrical relationship, we performed computer simulation based on our correlation-based self-organization model. The simulation showed that pinwheel centers tended to be located at the ocular dominance centers at higher correlations of activities between the left- and right-eye specific pathways, whereas they tended to appear along the borders of ocular dominance columns at lower correlations. This tendency was mathematically analyzed with a formula describing the condition determining the geometrical relationship between pinwheel centers and ocular dominance columns. Moreover, to examine the effect of activity correlations in the eye-specific pathways on the column formation, we conducted intrinsic signal optical imaging using normally reared cats and dark-reared cats. The between-eye activity correlation in dark-reared cats is expected to be lower than that in normal cats due to the lack of common visual input in the two eyes. The statistical analysis of experimental data showed that while more pinwheel centers tended to be located in the center subregion of ocular dominance columns than in the border subregion in the normal cats, a weak tendency in the opposite direction was found in the dark-reared cats. Based on the consistent results from the model and experiment, it is suggested that the activity correlation between the left- and right-eye specific pathways has influence on the establishment of geometrical relationship in the cortical representation between orientation preference and ocular dominance.

Orientation Plasticity in Visual Cortex of Mice Reared under Single-Orientation Exposure

To examine whether orientation selectivity in the mouse visual cortex can change depending on visual experience, we reared juvenile and adult mice under single-orientation exposure using cylindrical-lens-fitted goggles that extremely elongate visual images vertically. Immediately after goggle rearing, we performed optical imaging of intrinsic signals in the visual cortex of the mouse, while presenting 6 oriented grating stimuli. The distribution of preferred orientations was markedly biased toward the exposed vertical orientation in juvenile goggle-reared mice, whereas the distribution in normally reared mice showed a maximum at horizontal orientation and a minimum at vertical orientation. In contrast, no significant differences in the orientation distribution were found between 1-week goggle-reared and normally reared adult mice. However, in 2- or 3-week goggle-reared adult mice, the relative area maximally responding to the vertical orientation was slightly larger than that in normally reared adult mice whereas the horizontal bias was preserved. The present study demonstrated that postnatal visual experience can modify orientation selectivity in both juvenile and adult mice.