Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/138540
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dc.contributor.authorBosch, Carles-
dc.contributor.authorMartínez García, Albert-
dc.contributor.authorMasachs Janoher, Núria-
dc.contributor.authorTeixeira, Catia Marlene-
dc.contributor.authorFernaud, Isabel-
dc.contributor.authorUlloa Darquea, Fausto Alexander-
dc.contributor.authorPérez Martínez, Mª Esther-
dc.contributor.authorLois, Carlos-
dc.contributor.authorComella i Carnicé, Joan Xavier, 1963--
dc.contributor.authorDeFelipe, Javier-
dc.contributor.authorMerchán Pérez, Angel-
dc.contributor.authorSoriano García, Eduardo-
dc.date.accessioned2019-07-29T12:03:53Z-
dc.date.available2019-07-29T12:03:53Z-
dc.date.issued2015-05-21-
dc.identifier.issn1662-5129-
dc.identifier.urihttp://hdl.handle.net/2445/138540-
dc.description.abstractThe fine analysis of synaptic contacts is usually performed using transmission electron microscopy (TEM) and its combination with neuronal labeling techniques. However, the complex 3D architecture of neuronal samples calls for their reconstruction from serial sections. Here we show that focused ion beam/scanning electron microscopy (FIB/SEM) allows efficient, complete, and automatic 3D reconstruction of identified dendrites, including their spines and synapses, from GFP/DAB-labeled neurons, with a resolution comparable to that of TEM. We applied this technology to analyze the synaptogenesis of labeled adult-generated granule cells (GCs) in mice. 3D reconstruction of dendritic spines in GCs aged 3-4 and 8-9 weeks revealed two different stages of dendritic spine development and unexpected features of synapse formation, including vacant and branched dendritic spines and presynaptic terminals establishing synapses with up to 10 dendritic spines. Given the reliability, efficiency, and high resolution of FIB/SEM technology and the wide use of DAB in conventional EM, we consider FIB/SEM fundamental for the detailed characterization of identified synaptic contacts in neurons in a high-throughput manner.-
dc.format.extent17 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherFrontiers Media-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3389/fnana.2015.00060-
dc.relation.ispartofFrontiers In Neuroanatomy, 2015, vol. 9, p. 60-
dc.relation.urihttps://doi.org/10.3389/fnana.2015.00060-
dc.rightscc-by (c) Bosch, Carles et al., 2015-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es-
dc.sourceArticles publicats en revistes (Biologia Cel·lular, Fisiologia i Immunologia)-
dc.subject.classificationNeurones-
dc.subject.classificationSinapsi-
dc.subject.otherNeurons-
dc.subject.otherSynapses-
dc.titleFIB/SEM technology allows highthroughput 3D reconstruction of dendritic spines and synapses in GFP-traced adult-generated neurons-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec657440-
dc.date.updated2019-07-29T12:03:53Z-
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/604102/EU//HBP-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid26052271-
Appears in Collections:Articles publicats en revistes (Biologia Cel·lular, Fisiologia i Immunologia)
Publicacions de projectes de recerca finançats per la UE

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