The Role of LGN Directional Selectivity in Visual Cortical Processing
Project Number1R21EY030291-01A1
Contact PI/Project LeaderSWADLOW, HARVEY A
Awardee OrganizationUNIVERSITY OF CONNECTICUT STORRS
Description
Abstract Text
PROJECT SUMMARY
The lateral geniculate nucleus (LGN) of rabbits and rodents contains a population of neurons that
show strong directional selectivity (DS) to visual stimulation. Although these LGN DS neurons are
known to project to the primary visual cortex (V1), their synaptic targets, and their role in the synthesis
of V1 receptive fields are unknown. Whereas in cats and primates, LGN neurons display little or no
orientation and directional selectivity and these properties are thought to be largely synthesized within
V1, in rabbits and rodents these properties could potentially be inherited, in part, from the LGN DS
neurons. The proposed experiments will address this question, aiming to understand how LGN DS
neurons contribute to the synthesis of the diverse receptive field seen in V1 neurons. This will be
accomplished using two sets of complementary methods, in fully awake rabbits. First (Aim 1), we will
determine which layers of V1 receive a strong input from LGN DS neurons. We will do this using
single-axon spike-triggered current source-density analysis, a method that provides a view of the
laminar profile of the presynaptic (axonal) and monosynaptic local field potentials and currents
generated by the spikes of single thalamocortical neurons within the topographically aligned region of
recipient cortex. Next (Aim 2), we will record the spike trains of both LGN DS neurons, and
retinotopically aligned cortical neurons of different receptive field classes. We will determine which
cortical neurons within the synaptic recipient zone of the LGN DS neuron receives synaptic input
(using methods of extracellular cross-correlation), and how the directional preferences of the LGN DS
neurons relate to the preferences of their synaptic targets. Direction and orientation selectivity are
among the most salient response properties of visual cortical neurons and this project is aimed at
understanding how these properties emerge.
Public Health Relevance Statement
NARRATIVE
The current work will have an important impact on our understanding of how complex properties seen in
cortical neurons are synthesized and, more generally, it will contribute to our understanding of how
motion is perceived by the mammalian visual system. A disruption in motion perception is associated
numerous clinical disorders. A better understanding of the principals of motion perception will provide a
basis for future clinical studies of related to mental health, visual and behavioral disorders.
Eye Disease and Disorders of Vision; Neurosciences
Sub Projects
No Sub Projects information available for 1R21EY030291-01A1
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 1R21EY030291-01A1
Patents
No Patents information available for 1R21EY030291-01A1
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 1R21EY030291-01A1
Clinical Studies
No Clinical Studies information available for 1R21EY030291-01A1
News and More
Related News Releases
No news release information available for 1R21EY030291-01A1
History
No Historical information available for 1R21EY030291-01A1
Similar Projects
No Similar Projects information available for 1R21EY030291-01A1