Biomedical subjects

M G Rosa

Publications and source records attributed to M G Rosa.

46 records · Page 3Linked to original sources

PubMed1988

Complete pattern of ocular dominance stripes in V1 of a New World monkey, Cebus apella.

The presence of ocular dominance (OD) stripes in layer IVc of striate cortex (V1) is characteristic of all Old World simians so far studied. In contrast, some species of New World monkeys do not have ocular dominance stripes, and in those that do, the pattern of stripes may be different from that shown in Old World monkeys. This difference has led to the suggestion that OD stripes evolved independently in both groups. We have mapped the entire system of OD stripes in the New World monkey Cebus, by means of cytochrome oxidase histochemistry after monocular enucleation. A striking similarity was found between the patterns in Cebus and Macaca, which is suggestive of common ancestry, rather than parallel evolution.

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PubMed1987

Visual topography of V1 in the Cebus monkey.

The representation of the visual field in the striate cortex (V1) was mapped with multiunit electrodes in the Cebus monkey. Nine Cebus apella, anesthetized with N2O and immobilized with pancuromium bromide were studied in repeated recording sessions. In each hemisphere, V1 contains a continuous representation of the contralateral visual hemifield. The representation of the vertical meridian (VM) forms the external border of V1 except at the anteriormost portion of the calcarine fissure. The representation of the horizontal meridian (HM) divides the area so that the representation of the lower visual field is located dorsally, and that of the upper field ventrally. The convoluted surface of V1 can be only partially unfolded, and no precise "flattened" map can be obtained without introducing surface discontinuities. The visual topography of V1 is presented in a series of coronal sections and in "flattened" maps. The representation of the central visual field is magnified relative to that of the periphery in V1. The evaluation of the cortical magnification factors measured along isoeccentric and isopolar dimensions in the partially unfolded model of V1 revealed anisotropies in the representation of the visual field with larger magnification along isopolar lines than along isoeccentric lines. Receptive field size increases with increasing eccentricity, whereas point image size decreases with increasing eccentricity.

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PubMedDate not supplied

Cortical afferents of visual area MT in the Cebus monkey: possible homologies between New and Old World monkeys.

Cortical projections to the middle temporal (MT) visual area were studied by injecting the retrogradely transported fluorescent tracer Fast Blue into MT in adult New World monkeys (Cebus apella). Injection sites were selected based on electrophysiological recordings, and covered eccentricities from 2-70 deg, in both the upper and lower visual fields. The position and laminar distribution of labeled cell bodies were correlated with myeloarchitectonic boundaries and displayed in flat reconstructions of the neocortex. Topographically organized projections were found to arise mainly from the primary, second, third, and fourth visual areas (V1, V2, V3, and V4). Coarsely topographic patterns were observed in transitional V4 (V4t), in the parieto-occipital and parieto-occipital medial areas (PO and POm), and in the temporal ventral posterior area (TVP). In addition, widespread or nontopographic label was found in visual areas of the superior temporal sulcus (medial superior temporal, MST, and fundus of superior temporal, FST), annectent gyrus (dorsointermediate area, DI; and dorsomedial area, DM), intraparietal sulcus (lateral intraparietal, LIP; posterior intraparietal, PIP; and ventral intraparietal, VIP), and in the frontal eye field (FEF). Label in PO, POm, and PIP was found only after injections in the representation of the peripheral visual field (> 10 deg), and label in V4 and FST was more extensive after injections in the central representation. The projections from V1 and V2 originated predominantly from neurons in supragranular layers, whereas those from V3, V4t, DM, DI, POm, and FEF consisted of intermixed patches with either supragranular or infragranular predominance. All of the other projections were predominantly infragranular. Invasion of area MST by the injection site led to the labeling of further pathways, including substantial projections from the dorsal prelunate area (DP) and from an ensemble of areas located along the medial wall of the hemisphere. In addition, weaker projections were observed from the parieto-occipital dorsal area (POd), area 7a, area prostriata, the posterior bank of the arcuate sulcus, and areas in the anterior part of the lateral sulcus. Despite the different nomenclatures and areal boundaries recognized by different models of simian cortical organization, the pattern of projections to area MT is remarkably similar among primates. Our results provide evidence for the existence of many homologous areas in the extrastriate visual cortex of New and Old World monkeys.

Afferent Pathways↗

PubMedDate not supplied

Topography and extent of visual-field representation in the superior colliculus of the megachiropteran Pteropus.

It has been proposed that flying foxes (genus Pteropus) have a primate-like pattern of representation in the superficial layers of the superior colliculus (SC), whereby the visual representation in this structure is limited by the same decussation line that limits the retino-geniculo-cortical projection (Pettigrew, 1986). To test this hypothesis, visual receptive fields were plotted based on single- and multi-unit recordings in the SC of ten flying foxes. A complete representation of the contralateral hemifield was observed in the SC. Although the binocular hemifield of vision in Pteropus is 54 deg wide, receptive-field centers invaded the ipsilateral hemifield by only 8 deg, and the receptive-field borders by 13 deg. This invasion is similar to that observed at the border between visual areas V1 and V2 in the occipital cortex. The extent of the ipsilateral invasion was not affected by a lesion that completely ablated the occipital visual areas, thus suggesting that this invasion may be consequence of a zone of nasotemporal overlap in the retinal projections to the two colliculi. Neurones located in the superficial layers typically responded briskly to stimulation of both eyes, with a bias towards the contralateral eye. After cortical lesions the neuronal responses to the ipsilateral eye were depressed, and the ocular-dominance histograms shifted towards an even stronger dominance by the contralateral eye. However, cells located in the rostral pole of the SC remained responsive to the ipsilateral eye after cortical lesions. Responses in the stratum opticum and stratum griseum intermediale were more severely affected by cortical lesions than those in the stratum griseum superficiale. Our results demonstrate that the SC in flying foxes retain some generalized mammalian characteristics, such as the stronger direct projections of the contralateral eye and the location of the upper, lower, central, and peripheral representations in the SC. Nonetheless, the extent of visual representation in the SC demonstrates a specialized, primate-like pattern. These observations are consistent with the hypothesis that megachiropterans are members of a group that branched off early during the differentiation of primates from basal mammals.

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PubMedDate not supplied

Connectional and neurochemical subdivisions of the pulvinar in Cebus monkeys.

Based on cytoarchitectonic criteria, the primate pulvinar nucleus has been subdivided into medial (PM), lateral (PL), and inferior (PI) regions. However, these subdivisions show no correlation with those established by electrophysiological, immunocytochemical, or neuroanatomical tracer studies. In this work, we studied the connections of the pulvinar nucleus of Cebus monkey with visual areas V1, V2, V4, MT, and PO by means of retrograde fluorescent tracers injected into these areas. Based on the projection zones to cortical visual areas, the visual portion of the pulvinar of Cebus monkey was subdivided into three subregions: P1, P2, and P3, similar to those described in the macaque (Ungerleider et al., 1984). In Cebus, P1 includes the centrolateral portion of traditionally defined PI and adjacent portion of PL. P2 is located in the dorsal portion of PL and P3 includes the medial portion of PI and extends dorsally into adjacent PL and PM. In addition, we studied the histology of the pulvinar using multiple criteria, such as cytoarchitecture and myeloarchitecture; histochemistry for cytochrome oxidase, NADPH-diaphorase, and acetylcholinesterase; and immunocytochemistry for two calcium-binding proteins, calbindin and parvalbumin, and for a neurofilament recognized by the SMI-32 antibody. Some of these stains, mainly calbindin, showed additional subdivisions of the Cebus pulvinar, beyond the traditional PI, PL, and PM. Based on this immunohistochemical staining, the border of PI is moved dorsally above the brachium of the superior colliculus and PI can be subdivided in five regions (PI(P), PI(M), PI(C), PI(L), and PI(LS)). Regions P1, P2, and P3 defined based on efferent connections with cortical visual areas are not architectonically/neurochemically homogeneous. Rather they appear to consist of further chemoarchitectonic subdivisions. These distinct histochemical regions might be related to different functional modules of visual processing within one connectional area.

Acetylcholinesterase↗

PubMedDate not supplied

Organization of the second visual area in the megachiropteran bat Pteropus.

The organization of peristriate cortex was studied in nine flying foxes (genus Pteropus). Based on receptive field mapping and architectonic data, we report on the organization of the second visual area (V2). V2 forms a continuous belt 2-4 mm wide bordering V1 anteriorly. In each hemisphere, V2 contains a precisely organized representation of the entire contralateral visual field. The vertical meridian of the visual field (VM), and a short strip of the ipsilateral hemifield are represented at the posterior border of V2, with V1. The area centralis is represented approximately at the center of the posterior border of V2. At each mediolateral level, progressively more peripheral portions of the visual field are represented as V2 is crossed from posterior to anterior. The representation of the upper quadrant is continuous, and confined to the lateral half of V2. In contrast, the representation of the lower quadrant is split along a line running from the temporal edge of the field of vision to the optic disk. As a result of this arrangement, the portions of the lower quadrant close to the VM are represented medially, and those away from the VM laterally in V2. The entire representation of the horizontal meridian is located in lateral V2, and is not split between medial and lateral V2 as in primates. The linear cortical magnification factor (CMF) decays by a factor of 3-5 from the central to the peripheral representation. The CMF is anisotropic, and equal distances in the visual field are magnified twice as much parallel to the V1/V2 border than perpendicular to this border. Moreover, points in the lower quadrant are magnified relative to symmetrical points in the upper quadrant. V2 is histologically distinct from all surrounding areas in both cytochrome oxidase- and Nissl-stained sections. These results suggest that V2 is an homologous area common to all archontans, and imply that much of the variability reported among mammals may be due to technical factors, rather than true species differences.

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PubMedDate not supplied

Visuotopic reorganization in the primary visual cortex of adult cats following monocular and binocular retinal lesions.

The effect of discrete monocular retinal lesions on the representation of the visual field in the primary visual area (V1) was investigated in adult cats. Lesions were created using argon lasers, 8 d to 4(1/2) months prior to electrophysiological recording. This produced lesion projection zones (LPZs) in V1, 1.6-9.5 mm wide, that were deprived of their normal input from one eye, but that received a normal input from the other eye. Nevertheless, at the majority of recording sites within these zones neuronal responses were elicited by stimulation of the lesioned eye, with receptive fields being displaced onto regions of retina surrounding the lesion, while receptive fields determined through stimulation of the normal eye followed the normal visuotopic organization of V1. However, neuronal responses to stimulation of the lesioned eye within the LPZs were characterized by rapid habituation and unusually low firing rates in comparison with responses to stimulation of the normal eye. Stimulation of the normal eye temporarily marked the responsiveness of neurons within the LPZ to stimulation of the lesioned eye. The proportion of neurons responsive to stimulation of the lesioned eye was higher just inside the borders of the LPZs than at the centers of these zones. However, neurons responsive to stimulation of the test eye were found up to 3.6 mm from the perimeter of the LPZs, and therefore the shifts in the visuotopic map caused by retinal lesions cannot be explained solely on the basis of the normal scatter of receptive fields and point-image size in V1. The proportion of cells responsive to stimulation of the lesioned eye was highest in the infragranular layers, and lowest in the supragranular layers. By combining a restricted lesion of one eye with laser photocoagulation of the optic disc of the other eye, the effects of the normal eye on the lesion-induced visuotopic reorganization were also investigated. Neither chronic nor acute deactivation produced any discernible further changes in visuotopy or in the characteristics of neuronal responses to stimulation of the eye with the discrete lesions. Our findings show that the representations of the two eyes in adult visual cortex are capable of independent reorganization. These findings parallel those of work in auditory cortex, suggesting that topographic reorganization in primary sensory areas of adult cortex may be governed by similar mechanisms.

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PubMedDate not supplied

Comparison of dendritic fields of layer III pyramidal neurons in striate and extrastriate visual areas of the marmoset: a Lucifer yellow intracellular injection.

Basal dendritic field areas of layer III pyramidal neurons were compared between the first (V1), second (V2), dorsolateral (DL) and fundus of the superior temporal (FST) areas in marmoset monkey visual cortex. These areas correspond to early stages of visual processing (V1, V2) and to areas specialized for the analysis of shape (DL) and motion (FST). Neurons in fixed tangential cortical slices (250 microns) were injected with Lucifer Yellow and immunohistochemically processed for a diaminobenzidine reaction product. Dendritic field areas were calculated for layer III pyramidal cells whose complete basal projection was judged to be within the section (n = 189). Borders between different visual areas were established based on cytochrome oxidase immunohistochemistry and myelin patterns in the experimental hemisphere, and electrophysiological recordings in the contralateral hemisphere. Pyramidal neurons in V1 had a mean basal dendritic field area of 1.84 x 10(4) microns2 (SEM = 2.04 x 10(3) microns2; n = 21). Layer III pyramidal cells in V2 had a mean basal dendritic field 1.26 times larger (mean = 2.32 x 10(4) +/- 1.78 x 10(3) microns2; n = 42) than that of V1 neurons. The mean dendritic field area of layer III pyramidal cells in DL (n = 76) was 1.5 times larger than that in V1 (mean = 2.75 x 10(4) +/- 1.59 x 10(3) microns2), and that in FST (n = 50) was 2.3 times larger (mean = 4.26 x 10(4) +/- 2.79 x 10(3) microns2). Our results show that there is a correlation between tangential dendritic field area of basal dendrites of layer III pyramidal neurons and modality of visual processing. The increase in basal dendritic field area of layer III pyramidal cells may allow more extensive sampling of inputs as required by higher-order processing of visual information.

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PubMedDate not supplied

The occipitoparietal pathway of the macaque monkey: comparison of pyramidal cell morphology in layer III of functionally related cortical visual areas.

The dendritic morphology of pyramidal cells located at the base of layer III in the primary visual area (V1), the second visual area (V2), the middle temporal area (MT), the ventral portion of the lateral intraparietal area (LIPv) and in the portion of cytoarchitectonic area 7a within the anterior bank of the superior temporal sulcus was revealed by injecting neurons with Lucifer Yellow in fixed, flattened slices of macaque monkey visual cortex. These areas correspond to different levels of the occipitoparietal cortical 'stream', which processes information related to motion and spatial relationships in the visual field. The tissue was immunocytochemically processed to obtain a light-stable diaminobenzidine reaction product, revealing the dendritic morphology in fine detail. Retrogradely labelled MT-projecting neurons in supragranular V1 (layer IIIc of Hassler's nomenclature, corresponding to Brodmann's layer IVb) were predominantly pyramidal, although many spiny multipolar (stellate) cells were also found. The average basal dendritic field area of pyramidal neurons in sublamina IIIc of V1 was significantly smaller than that in the homologous layer of V2, within the cytochrome oxidase-rich thick stripes. Furthermore, the average basal dendritic field areas of V1 and V2 pyramidal neurons were significantly smaller than those of neurons in MT, LIPv and area 7a. There was no difference in basal dendritic field area between layer III pyramidal neurons in areas MT, LIPv and 7a. While the shape of most basal dendritic fields was circularly symmetrical in the dimension tangential to the cortical layers, there were significant biases in complexity, with dendritic branches tending to cluster along particular axes. Sholl analysis revealed that the dendritic fields of neurons in areas MT, LIPv and 7a were significantly more complex (i.e. had a larger number of branches) than those of V1 or V2 neurons. Analysis of basal dendritic spine densities revealed regional variations along the dendrites, with peak densities being observed 40-130 microns from the cell body, depending on the visual area. The peak spine density of layer III pyramidal neurons in V1 was lower than that observed in V2, MT or LIPv, which were all similar. Pyramidal neurons in area 7a had the greatest peak spine density, which was on average 1.7 times that found in V1. Calculations based on the average spine density and number of dendritic branches at different distances from the cell body demonstrated a serial increase in the total number of basal dendritic spines per neuron at successive stations of the occipitoparietal pathway. Our observations, comparing dendritic fields of neurons in the homologous cortical layer at different levels of a physiologically defined 'stream', indicate changes in pyramidal cell morphology between functionally related areas. The relatively large, complex, spine-dense dendritic fields of layer III pyramidal cells in rostral areas of the occipitoparietal pathway allow these cells to sample a greater number of more diverse inputs in comparison with cells in 'lower' areas of the proposed hierarchy.

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PubMedDate not supplied

Morphological variation of layer III pyramidal neurones in the occipitotemporal pathway of the macaque monkey visual cortex.

We compared the morphological characteristics of layer III pyramidal neurones in different visual areas of the occipitotemporal cortical 'stream', which processes information related to object recognition in the visual field (including shape, colour and texture). Pyramidal cells were intracellularly injected with Lucifer Yellow in cortical slices cut tangential to the cortical layers, allowing quantitative comparisons of dendritic field morphology, spine density and cell body size between the blobs and interblobs of the primary visual area (V1), the interstripe compartments of the second visual area (V2), the fourth visual area (V4) and cytoarchitectonic area TEO. We found that the tangential dimension of basal dendritic fields of layer III pyramidal neurones increases from caudal to rostral visual areas in the occipitotemporal pathway, such that TEO cells have, on average, dendritic fields spanning an area 5-6 times larger than V1 cells. In addition, the data indicate that V1 cells located within blobs have significantly larger dendritic fields than those of interblob cells. Sholl analysis of dendritic fields demonstrated that pyramidal cells in V4 and TEO are more complex (i.e. exhibit a larger number of branches at comparable distances from the cell body) than cells in V1 or V2. Moreover, this analysis demonstrated that the dendrites of many cells in V1 cluster along specific axes, while this tendency is less marked in extrastriate areas. Most notably, there is a relatively large proportion of neurones with 'morphologically orientation-biased' dendritic fields (i.e. branches tend to cluster along two diametrically opposed directions from the cell body) in the interblobs in V1, as compared with the blobs in V1 and extrastriate areas. Finally, counts of dendritic spines along the length of basal dendrites revealed similar peak spine densities in the blobs and the interblobs of V1 and in the V2 interstripes, but markedly higher spine densities in V4 and TEO. Estimates of the number of dendritic spines on the basal dendritic fields of layer III pyramidal cells indicate that cells in V2 have on average twice as many spines as V1 cells, that V4 cells have 3.8 times as many spines as V1 cells, and that TEO cells have 7.5 times as many spines as V1 cells. These findings suggest the possibility that the complex response properties of neurones in rostral stations in the occipitotemporal pathway may, in part, be attributed to their larger and more complex basal dendritic fields, and to the increase in both number and density of spines on their basal dendrites.

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