Mental retardation is caused by a variety of factors including mutations that affect brain development and therefore impair cognitive function. However, some of the genes involved in brain development may also have roles in the adult CNS. Disruption of these adult functions could result in learning deficits independently of any developmental abnormalities. Importantly, these post-development impairments in function may be more easily reversible than changes established during development. For example, previous studies involved the Notch pathway in neurogenesis. Additionally, recent findings demonstrated the expression of Notch 1 in the post-natal brain suggesting that this pathway may also have a role in modulating function in the adult brain. Additionally, recent findings demonstrated the expression of Notch 1 in the post-natal brain suggesting that this pathway also have a role in modulating function in the adult brain. Interestingly, our laboratory found that Notch 1 heterozygous mice (Notch+/-) have specific spatial learning and memory deficits, while motor coordination and other behaviors required to test spatial learning seemed unaffected by this mutation. Since Notch 1 is expressed in the adult hippocampus, we propose to study the impact of the Notch+/- mutation in hippocampal physiology and in other hippocampal-dependent learning and memory. To determine whether disruption of the Notch pathway specifically in adult neurons can affect cognitive function, we will take advantage of the LBD-inducible strategy that we recently used successfully to regulate the transcription factor CREB in adult mice. We will manipulate Notch function by fusing the RBP-J(R218H) dominant-negative gene with a mutant estrogen receptor ligand-binding domain (LBD/G521R). Injection of tamoxifen (the inducer) should trigger the activation of the Notch 1 dominant-negative repressor. We will use both types of mutant mice to address the following questions: 1- Is the Notch pathway required for learning and memory? Is it required for any other behaviors? 2- Is the Notch pathway required for hippocampal synaptic function?

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Center Core Grants (P30)
Project #
5P30HD004612-31
Application #
6483443
Study Section
National Institute of Child Health and Human Development Initial Review Group (CHHD)
Project Start
2001-07-01
Project End
2002-06-30
Budget Start
Budget End
Support Year
31
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Van, Christina; Condro, Michael C; Lov, Kenny et al. (2018) PACAP/PAC1 Regulation of Inflammation via Catecholaminergic Neurons in a Model of Multiple Sclerosis. J Mol Neurosci :
Ago, Yukio; Hayata-Takano, Atsuko; Kawanai, Takuya et al. (2017) Impaired extinction of cued fear memory and abnormal dendritic morphology in the prelimbic and infralimbic cortices in VPAC2 receptor (VIPR2)-deficient mice. Neurobiol Learn Mem 145:222-231
Yvone, Griselda M; Zhao-Fleming, Hannah H; Udeochu, Joe C et al. (2017) Disabled-1 dorsal horn spinal cord neurons co-express Lmx1b and function in nociceptive circuits. Eur J Neurosci 45:733-747
Krityakiarana, Warin; Zhao, Paul M; Nguyen, Kevin et al. (2016) Proof-of Concept that an Acute Trophic Factors Intervention After Spinal Cord Injury Provides an Adequate Niche for Neuroprotection, Recruitment of Nestin-Expressing Progenitors and Regeneration. Neurochem Res 41:431-49
Espinosa-Jeffrey, Araceli; Blanchi, Bruno; Biancotti, Juan Carlos et al. (2016) Efficient Generation of Viral and Integration-Free Human Induced Pluripotent Stem Cell-Derived Oligodendrocytes. Curr Protoc Stem Cell Biol 38:2D.18.1-2D.18.27
Condro, Michael C; Matynia, Anna; Foster, Nicholas N et al. (2016) High-resolution characterization of a PACAP-EGFP transgenic mouse model for mapping PACAP-expressing neurons. J Comp Neurol 524:3827-3848
Espinosa-Jeffrey, Araceli; Nguyen, Kevin; Kumar, Shalini et al. (2016) Simulated microgravity enhances oligodendrocyte mitochondrial function and lipid metabolism. J Neurosci Res 94:1434-1450
Krityakiarana, Warin; Zhao, Paul M; Nguyen, Kevin et al. (2016) Erratum to: Proof-of Concept that an Acute Trophic Factors Intervention After Spinal Cord Injury Provides an Adequate Niche for Neuroprotection, Recruitment of Nestin-Expressing Progenitors and Regeneration. Neurochem Res 41:1844
Abad, Catalina; Jayaram, Bhavaani; Becquet, Laurine et al. (2016) VPAC1 receptor (Vipr1)-deficient mice exhibit ameliorated experimental autoimmune encephalomyelitis, with specific deficits in the effector stage. J Neuroinflammation 13:169
Khankan, Rana R; Griffis, Khris G; Haggerty-Skeans, James R et al. (2016) Olfactory Ensheathing Cell Transplantation after a Complete Spinal Cord Transection Mediates Neuroprotective and Immunomodulatory Mechanisms to Facilitate Regeneration. J Neurosci 36:6269-86

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