Journal
MOLECULAR AND CELLULAR NEUROSCIENCE
Volume 46, Issue 1, Pages 45-54Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.mcn.2010.08.005
Keywords
GEF; Synaptic plasticity; Dendrite; Dendritic spine; Rac1; Knockout; Fear conditioning
Categories
Funding
- NIH-NIMH [R01MH071316, MH078064, MH57014, P01 MH074866]
- National Alliance for Autism Research (NAAR)
- National Alliance for Research on Schizophrenia and Depression (NARSAD)
- Alzheimer's Association
- Dunbar Funds
- NIH-NINDS [R37 NS034696]
- NINDS [5T32NS041234]
- NIH [1F31AG031621]
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Regulation of forebrain cellular structure and function by small GTPase pathways is crucial for normal and pathological brain development and function. Kalirin is a brain-specific activator of Rho-like small GTPases implicated in neuropsychiatric disorders. We have recently demonstrated key roles for kalirin in cortical synaptic transmission, dendrite branching, spine density, and working memory. However, little is known about the impact of the complete absence of kalirin on the hippocampus in mice. We thus investigated hippocampal function, structure, and associated behavioral phenotypes in KALRN knockout (KO) mice we have recently generated. Here we show that KALRN KO mice had modest impairments in hippocampal LW, but normal hippocampal synaptic transmission. In these mice, both context and cue-dependent fear conditioning were impaired. Spine density and dendrite morphology in hippocampal pyramidal neurons were not significantly affected in the KALRN KO mice, but small alterations in the gross morphology of the hippocampus were detected. These data suggest that hippocampal structure and function are more resilient to the complete loss of kalirin, and reveal impairments in fear learning. These studies allow the comparison of the phenotypes of different kalirin mutant mice and shed light on the brain region-specific functions of small GTPase signaling. (C) 2010 Elsevier Inc. All rights reserved.
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