The goals of this project are to determine the factors that regulate the differentiation neurons comprising the mammalian limbic system and to define the molecular mechanisms that mediate the formation of functional neural circuits during development. Our laboratory is most interested in gaining a basic understanding of these mechanisms in those parts of the mammalian central nervous system that mediate emotional behavior, memory and learning. We will characterize the role of cell surface proteins in the formation of connections, focusing prinicipally on the limbic system associated membrane protein (LAMP), 64,000 dalton glycoprotein isolated in our laboratory that is expressed early in development and may in part regulate the formation of limbic system connections. We propose 3 sets of experiments that will examine different aspects of the development of this system: 1) The role of LAMP and macromolecules carrying the HNK-1 carbohydrate epitope in the regulation of process differentiation and the innervation of targets by limbin neurons will continue to be evaluation in both roller tube explant and monolayer culture systems. 2) LAMP expression will be used as a marker in cortical transplant studies to evaluate the intrinsic and extrinsic factors that may mediate the commitment and differentiation of neurons destined for specific limbic cortical areas. 3) Molecular characterization of LAMP will continue by analyzing metabolic changes in LAMP during axonal growth and by purifying substantial amounts of LAMP to generate new mono- and polyclonal antibodies and in a collaborrative effort, deduce partial sequence information. In a second collaborative arrangement, we will perform expression library screening to isolate and clone the LAMP gene for subsequent sequence analysis and in situ localization of neurons expressing the LAMP gene. These basic developmental studies employ a variety of technical approaches, both anatomical and molecular, to address basic issues of neural circuit formation. Our long-term goal is to utilize this information to determine how developmental defects may result in specific behavioral abnormalities, and ultimately how these may be corrected.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37MH045507-07
Application #
2246629
Study Section
Special Emphasis Panel (NSS)
Project Start
1989-09-01
Project End
1999-08-31
Budget Start
1995-09-30
Budget End
1996-08-31
Support Year
7
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Medicine & Dentistry of NJ
Department
Neurosciences
Type
Schools of Medicine
DUNS #
622146454
City
Piscataway
State
NJ
Country
United States
Zip Code
08854
Qiu, Shenfeng; Champagne, Danielle L; Peters, Melinda et al. (2010) Loss of limbic system-associated membrane protein leads to reduced hippocampal mineralocorticoid receptor expression, impaired synaptic plasticity, and spatial memory deficit. Biol Psychiatry 68:197-204
Koshibu, Kyoko; Levitt, Pat (2008) Gene x environment effects: stress and memory dysfunctions caused by stress and gonadal factor irregularities during puberty in control and TGF-alpha hypomorphic mice. Neuropsychopharmacology 33:557-65
Persico, Antonio M; Di Pino, Giovanni; Levitt, Pat (2006) Multiple receptors mediate the trophic effects of serotonin on ventroposterior thalamic neurons in vitro. Brain Res 1095:17-25
Koshibu, Kyoko; Levitt, Pat (2006) Transforming growth factor-alpha induces sex-specific neurochemical imbalance in the stress- and memory-associated brain structures. Neuropharmacology 50:807-13
Persico, A M; Levitt, P; Pimenta, A F (2006) Polymorphic GGC repeat differentially regulates human reelin gene expression levels. J Neural Transm 113:1373-82
Koshibu, Kyoko; Ahrens, Eric T; Levitt, Pat (2005) Postpubertal sex differentiation of forebrain structures and functions depend on transforming growth factor-alpha. J Neurosci 25:3870-80
Torii, Masaaki; Levitt, Pat (2005) Dissociation of corticothalamic and thalamocortical axon targeting by an EphA7-mediated mechanism. Neuron 48:563-75
Dennis, Kathleen E; Levitt, Pat (2005) Regional expression of brain derived neurotrophic factor (BDNF) is correlated with dynamic patterns of promoter methylation in the developing mouse forebrain. Brain Res Mol Brain Res 140:1-9
Koshibu, K; Levitt, P (2005) Sex differences in expression of transforming growth factor-alpha and epidermal growth factor receptor mRNA in Waved-1 and C57Bl6 mice. Neuroscience 134:877-87
Bolz, Jurgen; Uziel, Daniela; Muhlfriedel, Sven et al. (2004) Multiple roles of ephrins during the formation of thalamocortical projections: maps and more. J Neurobiol 59:82-94

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