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dc.contributor.authorBosch, Carles
dc.contributor.authorMartinez, Albert
dc.contributor.authorMasachs, Nuria
dc.contributor.authorTeixeira, Catia M.
dc.contributor.authorFernaud, Isabel
dc.contributor.authorUlloa, Fausto
dc.contributor.authorPerez-Martinez, Esther
dc.contributor.authorLois, Carlos
dc.contributor.authorComella, Joan X.
dc.contributor.authorDeFelipe, Javier
dc.contributor.authorMerchan-Perez, Angel
dc.contributor.authorSoriano, Eduardo
dc.date2022-08-11T08:09:44.000
dc.date.accessioned2022-08-23T16:41:38Z
dc.date.available2022-08-23T16:41:38Z
dc.date.issued2015-05-21
dc.date.submitted2016-04-25
dc.identifier.citationFront Neuroanat. 2015 May 21;9:60. doi: 10.3389/fnana.2015.00060. eCollection 2015. <a href="http://dx.doi.org/10.3389/fnana.2015.00060">Link to article on publisher's site</a>
dc.identifier.issn1662-5129 (Linking)
dc.identifier.doi10.3389/fnana.2015.00060
dc.identifier.pmid26052271
dc.identifier.urihttp://hdl.handle.net/20.500.14038/39925
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.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=26052271&dopt=Abstract">Link to Article in PubMed</a>
dc.rights<p>Copyright © 2015 Bosch, Martínez, Masachs, Teixeira, Fernaud, Ulloa, Pérez-Martínez, Lois, Comella, DeFelipe, Merchán-Pérez and Soriano. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject3D-reconstruction
dc.subjectFIB/SEM
dc.subjectadult neurogenesis
dc.subjectdendritic spines
dc.subjectelectron microscopy
dc.subjectsynapses
dc.subjectDevelopmental Neuroscience
dc.titleFIB/SEM technology and high-throughput 3D reconstruction of dendritic spines and synapses in GFP-labeled adult-generated neurons
dc.typeJournal Article
dc.source.journaltitleFrontiers in neuroanatomy
dc.source.volume9
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=3735&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/2731
dc.identifier.contextkey8515413
refterms.dateFOA2022-08-23T16:41:39Z
html.description.abstract<p>The 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.</p>
dc.identifier.submissionpathoapubs/2731
dc.contributor.departmentLois Lab
dc.contributor.departmentNeurobiology
dc.source.pages60


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<p>Copyright © 2015 Bosch, Martínez, Masachs, Teixeira, Fernaud, Ulloa, Pérez-Martínez, Lois, Comella, DeFelipe, Merchán-Pérez and Soriano. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
Except where otherwise noted, this item's license is described as <p>Copyright © 2015 Bosch, Martínez, Masachs, Teixeira, Fernaud, Ulloa, Pérez-Martínez, Lois, Comella, DeFelipe, Merchán-Pérez and Soriano. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>