Abstract
Orientation preference maps (OPMs) are present in carnivores (such as cats and ferrets) and primates but are absent in rodents. In this study we investigate the possible link between astrocyte arbors and presence of OPMs. We simulate the development of orientation maps with varying hypercolumn widths using a variant of the Laterally Interconnected Synergetically Self-Organizing Map (LISSOM) model, the Gain Control Adaptive Laterally connected (GCAL) model, with an additional layer simulating astrocytic activation. The synaptic activity of V1 neurons is given as input to the astrocyte layer. The activity of this astrocyte layer is now used to modulate bidirectional plasticity of lateral excitatory connections in the V1 layer. By simply varying the radius of the astrocytes, the extent of lateral excitatory neuronal connections can be manipulated. An increase in the radius of lateral excitatory connections subsequently increases the size of a single hypercolumn in the OPM. When these lateral excitatory connections become small enough the OPM disappears and a salt-and-pepper organization emerges.
Highlights
The cortex is the outermost layer of cerebral tissue, composed of neuronal cell bodies and protoplasmic astroytes
Columns of neurons in the primary visual cortex (V1) are known to be tuned to visual stimuli containing edges of a particular orientation. The arrangement of these cortical columns varies across species. In many species such as in ferrets, cats, and monkeys a topology preserving map is observed, wherein tuned columns are observed in close proximity to each other, resulting in the formation of Orientation Preference Maps (OPMs)
We explore the role of astrocytes in the arrangement of these cortical columns using a self-organizing computational model
Summary
The cortex is the outermost layer of cerebral tissue, composed of neuronal cell bodies and protoplasmic astroytes. The 3-d volume of cortical tissue could be locally approximated as a 2-d sheet of nodes, with a single node representative of all the neurons within a particular column With this approximation it becomes possible to describe a 2-d map in the neuronal space with each node responding to a particular feature in the stimulus space. A model which simulates the development of such maps, would aid in understanding which factors contribute to the development of such features maps. These factors could include internal factors such as the connectivity between the nodes, or the available area of the cortex onto which the features are to be mapped. Features of the stimuli used for training the model themselves act as external factors
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