Neurons communicate using both chemical transmission at traditional synapses and electrical transmission through gap junctions. Electrical transmission is well studied in the mammalian retina, where gap junctions exist between all five major classes of neurons. Retinal ganglion cells (RGCs), the output cells of the retina, comprise ~40 functional types in mammals. Gap junctional coupling among RGCs has always been described as ?homotypic,? that is, between RGCs of the same type. We have discovered, for the first time, heterotypic electrical coupling in the mouse retina, between two RGCs of different types, called F-miniON and F-miniOFF RGCs. The existence of heterotypic RGC coupling breaks the rule of functional parallelism between RGC channels and requires new ideas about the role of coupling in retinal computation. This project aims to explore the functional role of heterotypic RGC coupling in the F-mini network through two specific aims.
In Aim 1 we will determine whether coupling between F-miniON and F-miniOFF RGCs creates a novel pathway for mixing ON and OFF signals in the inner retina.
In Aim 2 we will determine which features of moving stimuli are encoded by synchronized spiking between F-miniON and F-miniOFF RGCs. The proposed studies will advance our understanding of how chemical and electrical synaptic inputs interact to perform neural computations and how sharing of signals between parallel pathways contributes to sensory encoding.

Public Health Relevance

The goal of our research is to discover the mechanisms of visual computation in the retina. This proposal studies a novel circuit in two different types of retinal ganglion cells are electrically coupled. Our discovery of heterotypic coupling in retinal ganglion cells, the output cells of the retina, challenges a long-standing principle of functional parallelism, requiring new ideas about early stages of visual computation. This research will have impacts beyond the retina in revealing fundamental principles of neural circuit architecture and mechanism in line with the goals of the BRAIN initiative.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
1R01EY031329-01
Application #
9944076
Study Section
Neurotransporters, Receptors, and Calcium Signaling Study Section (NTRC)
Program Officer
Greenwell, Thomas
Project Start
2020-07-01
Project End
2025-04-30
Budget Start
2020-07-01
Budget End
2021-04-30
Support Year
1
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Northwestern University at Chicago
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611