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dc.contributor.authorGayoso, Jorge
dc.contributor.authorGarrosa, Manuel
dc.contributor.authorGayoso, Sara
dc.contributor.authorRodríguez-Arias, Carlos Alberto
dc.contributor.authorMartin-Ferrero, Miguel Ángel
dc.contributor.authorGayoso, Manuel José
dc.date.accessioned2024-12-20T08:13:10Z
dc.date.available2024-12-20T08:13:10Z
dc.date.issued2020
dc.identifier.citationMicron. May 2020 ;Vol.132:102841: p.1-6es
dc.identifier.issn0968-4328es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/72929
dc.descriptionProducción Científicaes
dc.description.abstractThe histological study of hard pieces such as tendons and calcified lesions and tissues is a field that has been gaining increased attention owing to the rapid development of implantable prostheses, among other factors. In these studies, serial sectioning is utilized to detect areas of interest throughout the entire piece, as it enables the application of the appropriate light and electron microscopy techniques in these areas. We propose the “threesectioning method” that subjects the pieces to three consecutive cycles of embedding and sectioning to localize and study the areas of interest, as an efficient technique for these histological studies. The pieces were first embedded in epoxy resin and then cut into thick sections (approximately 300 μm) for the first cycle. Next, areas of interest selected on these thick sections were re-embedded in epoxy resin to be sectioned again (second sectioning) to obtain a series of semithin sections (1–3 μm). These semithin sections are usually studied using the most relevant techniques for light microscopy. Smaller areas of interest are selected to be cut into ultrathin sections (60–90 nm) for transmission electron microscopy. If necessary, the selected areas of the semithin sections an be embedded again, and then cut into new ultrathin sections. The different kinds of sections we have described here may also be studied using scanning electron microscopy. This systematic method facilitates correlative microscopy from lower to higher magnifications along with the usage of a broad variety of histological techniques including electron microscopy.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherElsevieres
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccesses
dc.subject.classificationHard Tissue, Prostheses, Plastic Enbedding, Epoxy resin, Sectioning, Bone, Nerve, Thick sections, Ultrathin sections, TEM, SEM.es
dc.titleThree-sectioning method: A procedure for studying hard tissues and large pieces under light and electron microscopyes
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holderElsevieres
dc.identifier.doi10.1016/j.micron.2020.102841es
dc.relation.publisherversionhttps://www.elsevier.com/locate/micrones
dc.identifier.publicationfirstpage102841es
dc.identifier.publicationtitleMicrones
dc.identifier.publicationvolume132es
dc.peerreviewedSIes
dc.description.projectEste trabajo forma parte del proyecto de investigación financiado por la Junta de Castilla y León a través del Centro en Red de Medicina Regenerativaes
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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