The goal of this proposal is to determine the role that neural activity plays in the development of circuits within the retina. Specifically, we hope to gain insight into how signaling through NMDA receptors (NMDARs) contributes to the formation of excitatory circuits. We hypothesize that signaling through NMDARs is required for synapse formation between cone bipolar cells (cBCs) and retinal ganglion cells (RGCs). To test this hypothesis we have developed two aims.
In Aim 1, we will use transgenic mouse lines in which a single functional type of RGC is labeled to determine whether the subunit composition of NMDARs (eg. NR2A, NR2B) changes during development in each of several RGC types.
In Aim 2, we will use a mouse line in which RGCs lack functional NMDARs to determine whether NMDARs contribute to synapse formation between cBCs and RGCs. In the course of this work, we hope to improve our understanding of how synapse formation is regulated in the retina. Our findings will provide crucial insight that will guide future research aimed at developing strategies to promote synapse formation. These strategies might prove invaluable in developing therapies to treat the many retinal diseases that stem from cell death.

Public Health Relevance

In this study, we propose to test whether specific electrical and chemical activity is necessary for normal development of the connections between cells in the mammalian retina. This will extend our understanding of how the retina gives rise to sight and, ultimately, might lead to improvements in the treatment of both genetic and age-related retinal disorders that cause blindness.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32EY021063-02
Application #
8431733
Study Section
Special Emphasis Panel (ZRG1-F03B-H (20))
Program Officer
Greenwell, Thomas
Project Start
2010-12-01
Project End
2012-11-30
Budget Start
2011-12-01
Budget End
2012-11-30
Support Year
2
Fiscal Year
2012
Total Cost
$52,190
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Zhao, Xiwu; Stafford, Ben K; Godin, Ashley L et al. (2014) Photoresponse diversity among the five types of intrinsically photosensitive retinal ganglion cells. J Physiol 592:1619-36
Speer, Colenso M; Sun, Chao; Liets, Lauren C et al. (2014) Eye-specific retinogeniculate segregation proceeds normally following disruption of patterned spontaneous retinal activity. Neural Dev 9:25
Stafford, Benjamin K; Manookin, Michael B; Singer, Joshua H et al. (2014) NMDA and AMPA receptors contribute similarly to temporal processing in mammalian retinal ganglion cells. J Physiol 592:4877-89
Stafford, Benjamin K; Park, Silvia J H; Wong, Kwoon Y et al. (2014) Developmental changes in NMDA receptor subunit composition at ON and OFF bipolar cell synapses onto direction-selective retinal ganglion cells. J Neurosci 34:1942-8