Despite decades of research characterizing the structure and function of numerous cell types in the retina, the encoding properties of retinal amacrine cells remain largely unknown. The overall goal of my research is to contribute to our current understanding of visual processing in the retina by characterizing the intrinsic properties and connectivity of two newly identified retinal amacrine cell subtypes. To determine the physiological properties and synaptic microcircuitry of the CRH-1 retinal amacrine cell. I will be the first to (A) characterize the light responses of genetically labeled CRH-1 amacrine cells to a variety of visual stimuli. I will then (B) place CRH-1 into the context of a functional circuit by identifying postsynaptic retinal ganglion cells. These measurements will allow me determine whether CRH-1 cells could mediate feedforward inhibition in the inner retina. To examine the dynamics of gap-junctional coupling between nNOS-2 amacrine cells and the role of this network in visual processing. In preliminary experiments characterizing another genetically labeled amacrine cell, nNOS-2, I have discovered that these cells form an extensive coupled network. I will examine (A) whether nNOS-2 coupling is modulated by mean luminance and whether the modulatory signaling pathway involves dopamine or nitric oxide. I will also (B) determine how nNOS-2 coupling impacts visual response properties by measuring dendritic morphology and receptive fields in the same cells.

Public Health Relevance

The overall goal of my research is to understand how cell-specific neural circuits in the retina contribute to the processing of visual information. These studies are of great clinical importance because particular retinal diseases are likely to damage specific retinal circuits, and gaining a better understanding of the connectivity and function of each cell and circuit will enable the development of more targeted diagnostic tests and interventions.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32EY025930-01
Application #
8981864
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Agarwal, Neeraj
Project Start
2015-08-01
Project End
2018-07-31
Budget Start
2015-08-01
Budget End
2016-07-31
Support Year
1
Fiscal Year
2015
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
Jacoby, Jason; Nath, Amurta; Jessen, Zachary F et al. (2018) A Self-Regulating Gap Junction Network of Amacrine Cells Controls Nitric Oxide Release in the Retina. Neuron 100:1149-1162.e5
Jacoby, Jason; Schwartz, Gregory W (2017) Three Small-Receptive-Field Ganglion Cells in the Mouse Retina Are Distinctly Tuned to Size, Speed, and Object Motion. J Neurosci 37:610-625
Jacoby, Jason; Zhu, Yongling; DeVries, Steven H et al. (2015) An Amacrine Cell Circuit for Signaling Steady Illumination in the Retina. Cell Rep 13:2663-70