Title | Slitrk5 deficiency impairs corticostriatal circuitry and leads to obsessive-compulsive-like behaviors in mice. |
Publication Type | Journal Article |
Year of Publication | 2010 |
Authors | Shmelkov SV, Hormigo A, Jing D, Proenca CC, Bath KG, Milde T, Shmelkov E, Kushner JS, Baljevic M, Dincheva I, Murphy AJ, Valenzuela DM, Gale NW, Yancopoulos GD, Ninan I, Lee FS, Rafii S |
Journal | Nat Med |
Volume | 16 |
Issue | 5 |
Pagination | 598-602, 1p following 602 |
Date Published | 2010 May |
ISSN | 1546-170X |
Keywords | Animals, Behavior, Animal, Compulsive Behavior, Grooming, Membrane Proteins, Mice, Mice, Knockout, Neostriatum, Nerve Tissue Proteins, Obsessive-Compulsive Disorder, Synapses, Synaptic Transmission |
Abstract | Obsessive-compulsive disorder (OCD) is a common psychiatric disorder defined by the presence of obsessive thoughts and repetitive compulsive actions, and it often encompasses anxiety and depressive symptoms. Recently, the corticostriatal circuitry has been implicated in the pathogenesis of OCD. However, the etiology, pathophysiology and molecular basis of OCD remain unknown. Several studies indicate that the pathogenesis of OCD has a genetic component. Here we demonstrate that loss of a neuron-specific transmembrane protein, SLIT and NTRK-like protein-5 (Slitrk5), leads to OCD-like behaviors in mice, which manifests as excessive self-grooming and increased anxiety-like behaviors, and is alleviated by the selective serotonin reuptake inhibitor fluoxetine. Slitrk5(-/-) mice show selective overactivation of the orbitofrontal cortex, abnormalities in striatal anatomy and cell morphology and alterations in glutamate receptor composition, which contribute to deficient corticostriatal neurotransmission. Thus, our studies identify Slitrk5 as an essential molecule at corticostriatal synapses and provide a new mouse model of OCD-like behaviors. |
DOI | 10.1038/nm.2125 |
Alternate Journal | Nat. Med. |
PubMed ID | 20418887 |
PubMed Central ID | PMC2907076 |
Grant List | RC1 MH088814 / MH / NIMH NIH HHS / United States RC1 AI080309-01 / AI / NIAID NIH HHS / United States MH079513 / MH / NIMH NIH HHS / United States U01 HL066952 / HL / NHLBI NIH HHS / United States P50 MH079513 / MH / NIMH NIH HHS / United States RC1 MH088814-02 / MH / NIMH NIH HHS / United States RC1 AI080309 / AI / NIAID NIH HHS / United States R01 NS052819 / NS / NINDS NIH HHS / United States R01 NS052819-07 / NS / NINDS NIH HHS / United States R01 HL097797-02 / HL / NHLBI NIH HHS / United States R01 HL097797 / HL / NHLBI NIH HHS / United States / / Howard Hughes Medical Institute / United States AI080309 / AI / NIAID NIH HHS / United States HL097797 / HL / NHLBI NIH HHS / United States NS052819 / NS / NINDS NIH HHS / United States HL66592 / HL / NHLBI NIH HHS / United States U01 HL066952-010002 / HL / NHLBI NIH HHS / United States |