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Proc Natl Acad Sci U S A ; 102(39): 14052-7, 2005 Sep 27.
Article in English | MEDLINE | ID: mdl-16172381

ABSTRACT

The neuronal PAS domain protein 3 (NPAS3) gene encoding a brain-enriched transcription factor was recently found to be disrupted in a family suffering from schizophrenia. Mice harboring compound disruptions in the NPAS3 and related NPAS1 genes manifest behavioral and neuroanatomical abnormalities reminiscent of schizophrenia. Herein we demonstrate that Npas3-/- mice are deficient in expression of hippocampal FGF receptor subtype 1 mRNA, most notably in the dentate gyrus. In vivo BrdUrd-labeling shows that basal neural precursor cell proliferation in the dentate gyrus of Npas3-/- mice is reduced by 84% relative to wild-type littermates. We propose that a deficiency in adult neurogenesis may cause the behavioral and neuroanatomical abnormalities seen in Npas3-/- mice, and we speculate that impaired neurogenesis may be involved in the pathophysiology of schizophrenia.


Subject(s)
Basic Helix-Loop-Helix Transcription Factors/metabolism , Hippocampus/cytology , Neurons/cytology , Schizophrenia/genetics , Animals , Basic Helix-Loop-Helix Transcription Factors/genetics , Behavior, Animal , Cell Proliferation , Dentate Gyrus/anatomy & histology , Dentate Gyrus/chemistry , Dentate Gyrus/cytology , Dentate Gyrus/growth & development , Female , Fibroblast Growth Factor 2/pharmacology , Hippocampus/chemistry , Male , Mice , Mice, Neurologic Mutants , Neurons/metabolism , Neurons/physiology , Oligonucleotide Array Sequence Analysis , RNA, Messenger/metabolism , Schizophrenia/metabolism , Stem Cells/metabolism
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