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1.
Sci Rep ; 11(1): 4983, 2021 03 02.
Article in English | MEDLINE | ID: mdl-33654118

ABSTRACT

Quantitatively comparing brain-wide connectivity of different types of neuron is of vital importance in understanding the function of the mammalian cortex. Here we have designed an analytical approach to examine and compare datasets from hierarchical segmentation ontologies, and applied it to long-range presynaptic connectivity onto excitatory and inhibitory neurons, mainly located in layer 2/3 (L2/3), of mouse primary visual cortex (V1). We find that the origins of long-range connections onto these two general cell classes-as well as their proportions-are quite similar, in contrast to the inputs on to a cell type in L6. These anatomical data suggest that distal inputs received by the general excitatory and inhibitory classes of neuron in L2/3 overlap considerably.


Subject(s)
Neurons/physiology , Primary Visual Cortex , Synapses/physiology , Animals , Mice , Mice, Transgenic , Nerve Net/anatomy & histology , Nerve Net/physiology , Primary Visual Cortex/anatomy & histology , Primary Visual Cortex/physiology
2.
J Comp Neurol ; 529(1): 129-140, 2021 01.
Article in English | MEDLINE | ID: mdl-32361987

ABSTRACT

The extrageniculate visual pathway, which carries visual information from the retina through the superficial layers of the superior colliculus and the pulvinar, is poorly understood. The pulvinar is thought to modulate information flow between cortical areas, and has been implicated in cognitive tasks like directing visually guided actions. In order to better understand the underlying circuitry, we performed retrograde injections of modified rabies virus in the visual cortex and pulvinar of the Long-Evans rat. We found a relatively small population of cells projecting to primary visual cortex (V1), compared to a much larger population projecting to higher visual cortex. Reciprocal corticothalamic projections showed a similar result, implying that pulvinar does not play as big a role in directly modulating rodent V1 activity as previously thought.


Subject(s)
Primary Visual Cortex/anatomy & histology , Pulvinar/anatomy & histology , Visual Pathways/anatomy & histology , Animals , Female , Primary Visual Cortex/cytology , Pulvinar/cytology , Rats , Rats, Long-Evans , Visual Cortex/anatomy & histology , Visual Cortex/cytology , Visual Pathways/cytology
3.
Curr Biol ; 31(4): 733-741.e7, 2021 02 22.
Article in English | MEDLINE | ID: mdl-33275889

ABSTRACT

Orientation preference maps (OPMs) are a prominent feature of primary visual cortex (V1) organization in many primates and carnivores. In rodents, neurons are not organized in OPMs but are instead interspersed in a "salt and pepper" fashion, although clusters of orientation-selective neurons have been reported. Does this fundamental difference reflect the existence of a lower size limit for orientation columns (OCs) below which they cannot be scaled down with decreasing V1 size? To address this question, we examined V1 of one of the smallest living primates, the 60-g prosimian mouse lemur (Microcebus murinus). Using chronic intrinsic signal imaging, we found that mouse lemur V1 contains robust OCs, which are arranged in a pinwheel-like fashion. OC size in mouse lemurs was found to be only marginally smaller compared to the macaque, suggesting that these circuit elements are nearly incompressible. The spatial arrangement of pinwheels is well described by a common mathematical design of primate V1 circuit organization. In order to accommodate OPMs, we found that the mouse lemur V1 covers one-fifth of the cortical surface, which is one of the largest V1-to-cortex ratios found in primates. These results indicate that the primate-type visual cortical circuit organization is constrained by a size limitation and raises the possibility that its emergence might have evolved by disruptive innovation rather than gradual change.


Subject(s)
Cheirogaleidae , Primary Visual Cortex/anatomy & histology , Primary Visual Cortex/physiology , Animals , Cheirogaleidae/anatomy & histology , Cheirogaleidae/physiology , Female , Male , Models, Neurological , Neurons/physiology , Orientation , Primary Visual Cortex/cytology
4.
Cereb Cortex ; 30(6): 3483-3517, 2020 05 18.
Article in English | MEDLINE | ID: mdl-31897474

ABSTRACT

The cerebral cortex of primates encompasses multiple anatomically and physiologically distinct areas processing visual information. Areas V1, V2, and V5/MT are conserved across mammals and are central for visual behavior. To facilitate the generation of biologically accurate computational models of primate early visual processing, here we provide an overview of over 350 published studies of these three areas in the genus Macaca, whose visual system provides the closest model for human vision. The literature reports 14 anatomical connection types from the lateral geniculate nucleus of the thalamus to V1 having distinct layers of origin or termination, and 194 connection types between V1, V2, and V5, forming multiple parallel and interacting visual processing streams. Moreover, within V1, there are reports of 286 and 120 types of intrinsic excitatory and inhibitory connections, respectively. Physiologically, tuning of neuronal responses to 11 types of visual stimulus parameters has been consistently reported. Overall, the optimal spatial frequency (SF) of constituent neurons decreases with cortical hierarchy. Moreover, V5 neurons are distinct from neurons in other areas for their higher direction selectivity, higher contrast sensitivity, higher temporal frequency tuning, and wider SF bandwidth. We also discuss currently unavailable data that could be useful for biologically accurate models.


Subject(s)
Visual Cortex/anatomy & histology , Visual Cortex/physiology , Visual Pathways/anatomy & histology , Visual Pathways/physiology , Animals , Geniculate Bodies/anatomy & histology , Geniculate Bodies/physiology , Macaca , Neurons/cytology , Neurons/physiology , Primary Visual Cortex/anatomy & histology , Primary Visual Cortex/cytology , Primary Visual Cortex/physiology , Visual Cortex/cytology
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