New functions of Semaphorin 3E and its receptor PlexinD1 during developing and adult hippocampal formation

dc.contributor.authorMata Rodríguez, Agata
dc.contributor.authorGil Fernández, Vanessa
dc.contributor.authorPérez Clausell, Jeús
dc.contributor.authorDasilva, Miguel
dc.contributor.authorGonzález-Calixto, Mari Carmen
dc.contributor.authorSoriano García, Eduardo
dc.contributor.authorGarcía-Verdugo, José Manuel
dc.contributor.authorSánchez-Vives, María Victoria
dc.contributor.authorRío Fernández, José Antonio del
dc.date.accessioned2018-11-09T14:43:49Z
dc.date.available2018-11-09T14:43:49Z
dc.date.issued2018-01-22
dc.date.updated2018-11-09T14:43:50Z
dc.description.abstractThe development and maturation of cortical circuits relies on the coordinated actions of long and short range axonal guidance cues. In this regard, the class 3 semaphorins and their receptors have been seen to be involved in the development and maturation of the hippocampal connections. However, although the role of most of their family members have been described, very few data about the participation of Semaphorin 3E (Sema3E) and its receptor PlexinD1 during the development and maturation of the entorhino-hippocampal (EH) connection are available. In the present study, we focused on determining their roles both during development and in adulthood. We determined a relevant role for Sema3E/PlexinD1 in the layer-specific development of the EH connection. Indeed, mice lacking Sema3E/PlexinD1 signalling showed aberrant layering of entorhinal axons in the hippocampus during embryonic and perinatal stages. In addition, absence of Sema3E/PlexinD1 signalling results in further changes in postnatal and adult hippocampal formation, such as numerous misrouted ectopic mossy fibers. More relevantly, we describe how subgranular cells express PlexinD1 and how the absence of Sema3E induces a dysregulation of the proliferation of dentate gyrus progenitors leading to the presence of ectopic cells in the molecular layer. Lastly, Sema3E mutant mice displayed increased network excitability both in the dentate gyrus and the hippocampus proper.
dc.format.extent16 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec680430
dc.identifier.issn2045-2322
dc.identifier.pmid29358640
dc.identifier.urihttps://hdl.handle.net/2445/125965
dc.language.isoeng
dc.publisherNature Publishing Group
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1038/s41598-018-19794-0
dc.relation.ispartofScientific Reports, 2018, vol. 8, p. 1381
dc.relation.urihttps://doi.org/10.1038/s41598-018-19794-0
dc.rightscc-by (c) Mata, Agata et al., 2018
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Biologia Cel·lular, Fisiologia i Immunologia)
dc.subject.classificationNeurobiologia del desenvolupament
dc.subject.classificationProteïnes
dc.subject.otherDevelopmental neurobiology
dc.subject.otherProteins
dc.titleNew functions of Semaphorin 3E and its receptor PlexinD1 during developing and adult hippocampal formation
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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