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GAP43 Located on Corticostriatal Terminals Restrains Novelty-Induced Hyperactivity in Mice

dc.contributor.authorMaroto Martínez, Irene Berenice
dc.contributor.authorCostas Insúa, Carlos
dc.contributor.authorMontero Fernández, Carlos
dc.contributor.authorHermoso-López, Alba
dc.contributor.authorLebouc, Margaux
dc.contributor.authorBajo Grañeras, Raquel
dc.contributor.authorÁlvaro-Blázquez, Alicia
dc.contributor.authorBlázquez Ortiz, Cristina
dc.contributor.authorCannich, Astrid
dc.contributor.authorMarsicano, Giovanni
dc.contributor.authorMartín Herranz, Ricardo
dc.contributor.authorBaufreton, Jérôme
dc.contributor.authorRodríguez Crespo, José Ignacio
dc.contributor.authorBellocchio, Luigi
dc.contributor.authorGuzmán Pastor, Manuel
dc.date.accessioned2025-01-14T10:00:03Z
dc.date.available2025-01-14T10:00:03Z
dc.date.issued2024-07-31
dc.descriptionSignificance Statement Psychiatric alterations such as attention deficit/hyperactivity disorder, schizophrenia, and bipolar disorder pose a significant health and socioeconomic burden to our society. Animal models that recapitulate precise phenotypic traits of those diseases are therefore warranted for developing new therapeutic interventions. Here, we found that mice lacking the protein GAP43 selectively in telencephalic glutamatergic neurons show a robust novelty-induced hyperactive phenotype, a behavioral deficit often associated to psychiatric diseases. These mice exhibit profound alterations in corticostriatal excitatory plasticity and a selective overactivation of dorsal-striatum neurons in response to a novel environment. Our findings thus unveil an important role of GAP43 in corticostriatal function and provide a new animal model with a delimited neuronal-circuit alteration for studying novelty-induced hyperactivity in psychiatric disorders.
dc.description.abstractGrowth-associated protein of 43 kDa (GAP43) is a key cytoskeleton-associated component of the presynaptic terminal that facilitates neuroplasticity. Downregulation of GAP43 expression has been associated to various psychiatric conditions in humans and evokes hippocampus-dependent memory impairments in mice. Despite the extensive studies conducted on hippocampal GAP43 in past decades, however, very little is known about its roles in modulating the excitatory versus inhibitory balance in other brain regions. We recently generated conditional knock-out mice in which the Gap43 gene was selectively inactivated in either telencephalic glutamatergic neurons (Gap43fl/fl;Nex1Cre mice, hereafter Glu-GAP43−/− mice) or forebrain GABAergic neurons (Gap43fl/fl;Dlx5/6Cre mice, hereafter GABA-GAP43−/− mice). Here, we show that Glu-GAP43−/− but not GABA-GAP43−/−mice of either sex show a striking hyperactive phenotype when exposed to a novel environment. This behavioral alteration of Glu-GAP43−/− mice was linked to a selective activation of dorsal-striatum neurons, as well as to an enhanced corticostriatal glutamatergic transmission and an abrogation of corticostriatal endocannabinoid-mediated long-term depression. In line with these observations, GAP43 was abundantly expressed in corticostriatal glutamatergic terminals of wild-type mice. The novelty-induced hyperactive phenotype of Glu-GAP43−/− mice was abrogated by chemogenetically inhibiting corticostriatal afferences with a Gi-coupled “designer receptor exclusively activated by designer drugs” (DREADDs), thus further supporting that novelty-induced activity is controlled by GAP43 at corticostriatal excitatory projections. Taken together, these findings show an unprecedented regulatory role of GAP43 in the corticostriatal circuitry and provide a new mouse model with a delimited neuronal-circuit alteration for studying novelty-induced hyperactivity, a phenotypic shortfall that occurs in diverse psychiatric diseases.
dc.description.departmentDepto. de Bioquímica y Biología Molecular
dc.description.facultyFac. de Ciencias Químicas
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipMICINN/FEDER
dc.description.statuspub
dc.identifier.citationMaroto IB, Costas-Insua C, Montero-Fernández C, Hermoso-López A, Lebouc M, Bajo-Grañeras R, Álvaro-Blázquez A, Blázquez-Ortiz C, Cannich A, Marsicano M, Martín R, Baufreton J, Rodríguez-Crespo I, Bellocchio L y Guzmán M. GAP43 Located on Corticostriatal Terminals Restrains Novelty-Induced Hyperactivity in Mice. J Neurosci . 2024 Sep 25;44(39):e0701242024. doi: 10.1523/JNEUROSCI.0701-24.2024.
dc.identifier.doi10.1523/JNEUROSCI.0701-24.2024
dc.identifier.issn1529-2401
dc.identifier.officialurlhttps://www.jneurosci.org/content/44/39/e0701242024
dc.identifier.pmid39168654
dc.identifier.urihttps://hdl.handle.net/20.500.14352/114180
dc.issue.number39
dc.journal.titleThe Journal of Neuroscience
dc.language.isoeng
dc.page.initiale0701242024
dc.publisherJournal of Neuroscience
dc.relation.projectIDRTI2018-095311-B-I00
dc.relation.projectIDPID2021-125118OB-I00
dc.rights.accessRightsopen access
dc.subject.cdu577.1
dc.subject.keywordCannabinoide
dc.subject.keywordCircuito corticoestriatal
dc.subject.keywordGAP43
dc.subject.keywordTransmisión glutamatérgica
dc.subject.keywordLong-term depression
dc.subject.keywordActividad motora
dc.subject.ucmCiencias Biomédicas
dc.subject.ucmNeurociencias (Biológicas)
dc.subject.ucmBioquímica (Biología)
dc.subject.ucmBiología molecular (Biología)
dc.subject.unesco24 Ciencias de la Vida
dc.subject.unesco2490 Neurociencias
dc.subject.unesco2403 Bioquímica
dc.subject.unesco2415 Biología Molecular
dc.subject.unesco2406 Biofísica
dc.titleGAP43 Located on Corticostriatal Terminals Restrains Novelty-Induced Hyperactivity in Mice
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number44
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscoveryf91524de-7b0c-458e-8c4a-d41a4c7d39d2

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