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dc.contributor.authorCasas-Torremocha, Diana
dc.contributor.authorPorrero, César
dc.contributor.authorRodriguez-Moreno, Javier
dc.contributor.authorGarcía-Amado, María
dc.contributor.authorLübke, Joachim H.R.
dc.contributor.authorNúñez Molina, Ángel 
dc.contributor.authorClascá, Francisco
dc.contributor.otherUAM. Departamento de Anatomía, Histología y Neurocienciaes_ES
dc.date.accessioned2019-10-24T15:19:11Z
dc.date.available2019-10-24T15:19:11Z
dc.date.issued2019-03-27
dc.identifier.citationBrain Structure and Function 224.4 (2019):1627-1645en_US
dc.identifier.issn1863-2653 (print)es_ES
dc.identifier.issn1863-2661 (online)es_ES
dc.identifier.urihttp://hdl.handle.net/10486/688975
dc.description.abstractRodents extract information about nearby objects from the movement of their whiskers through dynamic computations that are carried out by a network of forebrain structures that includes the thalamus and the primary sensory (S1BF) and motor (M1wk) whisker cortices. The posterior nucleus (Po), a higher order thalamic nucleus, is a key hub of this network, receiving cortical and brainstem sensory inputs and innervating both motor and sensory whisker-related cortical areas. In a recent study in rats, we showed that Po inputs differently impact sensory processing in S1BF and M1wk. Here, in C57BL/6 mice, we measured Po synaptic bouton layer distribution and size, compared cortical unit response latencies to “in vivo” Po activation, and pharmacologically examined the glutamatergic receptor mechanisms involved. We found that, in S1BF, a large majority (56%) of Po axon varicosities are located in layer (L)5a and only 12% in L2–L4, whereas in M1wk this proportion is inverted to 18% and 55%, respectively. Light and electron microscopic measurements showed that Po synaptic boutons in M1wk layers 3–4 are significantly larger (~ 50%) than those in S1BF L5a. Electrical Po stimulation elicits different area-specific response patterns. In S1BF, responses show weak or no facilitation, and involve both ionotropic and metabotropic glutamate receptors, whereas in M1wk, unit responses exhibit facilitation to repetitive stimulation and involve ionotropic NMDA glutamate receptors. Because of the different laminar distribution of axon terminals, synaptic bouton size and receptor mechanisms, the impact of Po signals on M1wk and S1BF, although simultaneous, is likely to be markedly different.en_US
dc.description.sponsorshipThis study was supported by European Union’s Horizon 2020 (Grant Agreement no. 785907 HBP SGA2) and Ministerio de Economía y Competitividad/Fondo Europeo para el Desarrollo Regional (MINECO/FEDER) Grant BFU2017-88549 to F.C., and MINECO/FEDER Grant BFU2012-36107 to A.N.en_US
dc.format.extent19 pag.es_ES
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherSpringer (part of Springer Nature)en_US
dc.relation.ispartofBrain Structure and Functionen_US
dc.rights© 2019, The Author(s).en_US
dc.subject.otherCerebral cortexen_US
dc.subject.otherExcitatory synaptic boutonsen_US
dc.subject.otherHigher order thalamusen_US
dc.subject.otherMetabotropic receptorsen_US
dc.subject.otherNMDA receptorsen_US
dc.subject.otherThalamocortical projectionsen_US
dc.titlePosterior thalamic nucleus axon terminals have different structure and functional impact in the motor and somatosensory vibrissal corticesen_US
dc.typearticleen
dc.subject.ecienciaMedicinaes_ES
dc.relation.publisherversionhttps://doi.org/10.1007/s00429-019-01862-4es_ES
dc.identifier.doi10.1007/s00429-019-01862-4es_ES
dc.identifier.publicationfirstpage1627es_ES
dc.identifier.publicationissue4es_ES
dc.identifier.publicationlastpage1645es_ES
dc.identifier.publicationvolume224es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/785907/EU//HBP SGA2es_ES
dc.relation.projectIDGobierno de España. BFU2017-88549es_ES
dc.relation.projectIDGobierno de España. BFU2012-36107es_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.rights.ccReconocimientoes_ES
dc.rights.accessRightsopenAccessen
dc.authorUAMCasas Torremocha, Diana (281230)
dc.authorUAMClasca Cabre, Francisco (259664)
dc.authorUAMPorrero Calzado, Cesar (261418)
dc.authorUAMRodríguez Moreno, Javier (262570)
dc.authorUAMNúñez Molina, Ángel (259225)
dc.facultadUAMFacultad de Medicina


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