An essential step in understanding sensory processing is to identify the synaptic circuitry underlying its neural representation. Aberrant network activity that disrupts excitation-inhibition balance can have severe consequences, contributing to the development of epilepsy, schizophrenia or Parkinson's disease. Identifying the mechanisms for the spread of excitation will directly inform about potential abnormalities that arise under pathological conditions. Thalamic projections to cortical layer 4 (L4) are the primary pathway by which sensory information enters the cortex via the thalamus. Information is thought to flow along a hierarchical series of connections from L4 to superficial L2/3, to the output cells in L5/6. However, thalamic neurons send sparse projections to virtually all layers of cortex, notably to the L5/L6 border. Mechanisms may exist that render sparse projections, often ignored in the study of circuits, highly effective in spreading excitatory activity. This would suggest a more complex mechanism of sensory information processing than previously thought, by which information relayed by thalamus reaches cortical output neurons via direct parallel pathways. Using optogenetics, electrophysiology, and behavioral paradigms, we propose to demonstrate that direct thalamocortical inputs can strongly, and directly drive L5 output neurons without L4 activity, and determine how the direct and indirect pathways affect sensory behavior.

Public Health Relevance

Detailed knowledge about the organization and function of cortical circuitry is a necessary first step in understanding the mechanism of cortical information processing. Aberrant network activity that disrupts excitation-inhibition balance can have severe consequences, contributing to the development of epilepsy, schizophrenia and Parkinson's disease. The proposed studies will characterize the mechanisms for the spread of excitation, which can directly inform about abnormalities that arise under pathological conditions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32NS084768-01
Application #
8595873
Study Section
Special Emphasis Panel (ZRG1-F02B-D (20))
Program Officer
Gnadt, James W
Project Start
2013-06-01
Project End
2015-05-31
Budget Start
2013-06-01
Budget End
2014-05-31
Support Year
1
Fiscal Year
2013
Total Cost
$53,942
Indirect Cost
Name
Columbia University (N.Y.)
Department
Neurosciences
Type
Schools of Medicine
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Hong, Y Kate; Lacefield, Clay O; Rodgers, Chris C et al. (2018) Sensation, movement and learning in the absence of barrel cortex. Nature 561:542-546