The long-term objective is to delineate the cellular mechanisms by which spontaneous correlated neural activity is generated in the developing mammalian retina. Very early in brain development, before sensory experience is possible, both electrical and chemical activity is generated spontaneously throughout the immature nervous system. There is growing evidence that this early activity is critical for the appropriate development of neural circuits. Developing a detailed understanding of the organizing principles that govern the normal development of the human nervous system may make it possible to understand the origin of neurological birth defects. In addition, it will provide critical insights into devising strategies that allow the nervous system to rewire normal functioning neural circuits in response to developmental abnormalities such as amblyopia (lazy eye). The cellular basis of spontaneous activity in the retina has been studied primarily by electrophysiology and calcium imaging. Spontaneous retinal activity is characterized by depolarizations that occur with a period on the order of minutes. Indeed, we can reproduce this slow periodicity in dissociated retina neurons, indicating that the pacemaker underlying this periodicity may be cell autonomous. Here we propose to test the hypothesis that this slow periodicity is set by oscillations in the second messenger, cAMP. The goals of this proposal are two fold. First, we propose to implement in retinal neurons the use of two indicators - one sensitive to levels of the second-messenger cAMP levels, and the second sensitive to activity of protein kinase-A. Second, we will then use these indicators to determine whether spontaneous oscillations in cAMP underlie the periodicity observed in both the intact retina as well spontaneously active networks formed by dissociated retinal neurons.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21EY016417-01
Application #
6903059
Study Section
Neurodifferentiation, Plasticity, and Regeneration Study Section (NDPR)
Program Officer
Hunter, Chyren
Project Start
2005-05-01
Project End
2007-03-31
Budget Start
2005-05-01
Budget End
2006-03-31
Support Year
1
Fiscal Year
2005
Total Cost
$215,290
Indirect Cost
Name
University of California San Diego
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Dunn, Timothy A; Storm, Daniel R; Feller, Marla B (2009) Calcium-dependent increases in protein kinase-A activity in mouse retinal ganglion cells are mediated by multiple adenylate cyclases. PLoS One 4:e7877
Dunn, Timothy A; Feller, Marla B (2008) Imaging second messenger dynamics in developing neural circuits. Dev Neurobiol 68:835-44
Wang, Chih-Tien; Blankenship, Aaron G; Anishchenko, Anastasia et al. (2007) GABA(A) receptor-mediated signaling alters the structure of spontaneous activity in the developing retina. J Neurosci 27:9130-40
Firth, Sally I; Feller, Marla B (2006) Dissociated GABAergic retinal interneurons exhibit spontaneous increases in intracellular calcium. Vis Neurosci 23:807-14
Dunn, Timothy A; Wang, Chih-Tien; Colicos, Michael A et al. (2006) Imaging of cAMP levels and protein kinase A activity reveals that retinal waves drive oscillations in second-messenger cascades. J Neurosci 26:12807-15