Alterations of visual experience in development induce dramatic reorganization of connections in the primary visual cortex. The capacity for experience-dependent plasticity declines with age. Visual cortical plasticity requires the activation of the cAMP responsive element (CRE) signaling pathway, an activity-dependent cascade that leads to gene expression. The objective of this proposal is to better define the involvement of calcium and cAMP-dependent signaling components in visual cortical plasticity. The primary model that we use is the monocular deprivation effect, which refers to changes in visual cortical function and morphology induced by monocular deprivation. Our hypotheses are that regulation of CRE/CREB signaling underlies the loss of plasticity with age and that ERK, p90RSK, and CREB play distinct roles in the plasticity mechanism. Specifically, the major questions addressed by the proposed experiments are: (1) Does CREB activity regulate the critical period for ocular dominance plasticity? We will use transgenic mice engineered to have regulatable enhancement of CREB function in the adult. (2) Is p90RSK the regulatory switch for activity dependent gene expression in the visual cortex? We will express a mutant form of RSK2 to examine whether RSK activity controls CRE-mediated gene expression and visual cortical plasticity. (3) How are signaling components of the CRE/CREB pathway regulated in the visual cortex? We will use biochemical approaches to elucidate the interactions of different signaling components in the visual cortex. (4) How do CREB, ERK, p90RSK, and activity interact to regulate the dendritic morphology of visual cortical neurons? We will use viral system that expresses mutant forms of signaling molecules together with GFP in order to assess the role of these signaling proteins in the control of dendritic morphology. It is our hope that this research will shed light on basic mechanisms underlying developmental plasticity and why it declines with age. Our findings may help in the development of therapies to enhance plasticity in the developing and mature brain, potentially allowing treatments for central visual dysfunction and other intractable brain disorders.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
1R01EY014238-01A2
Application #
6728723
Study Section
Molecular, Cellular and Developmental Neurosciences 2 (MDCN)
Program Officer
Oberdorfer, Michael
Project Start
2004-02-01
Project End
2004-08-31
Budget Start
2004-02-01
Budget End
2004-08-31
Support Year
1
Fiscal Year
2004
Total Cost
$51,256
Indirect Cost
Name
University of Washington
Department
Psychiatry
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Fischer, Quentin S; Graves, Aundrea; Evans, Scott et al. (2007) Monocular deprivation in adult mice alters visual acuity and single-unit activity. Learn Mem 14:277-86
Fischer, Quentin S; Aleem, Salman; Zhou, Hongyi et al. (2007) Adult visual experience promotes recovery of primary visual cortex from long-term monocular deprivation. Learn Mem 14:573-80
Cao, Zhiping; Liu, Lijuan; Lickey, Marvin et al. (2007) Virally mediated knock-down of NR2 subunits ipsilateral to the deprived eye blocks ocular dominance plasticity. Exp Brain Res 177:64-77
Suzuki, Seigo; Zhou, Hongyi; Neumaier, John F et al. (2007) Opposing functions of CREB and MKK1 synergistically regulate the geometry of dendritic spines in visual cortex. J Comp Neurol 503:605-17