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    •   UVaDOC Principal
    • PRODUCCIÓN CIENTÍFICA
    • Departamentos
    • Dpto. Biología Celular, Genética, Histología y Farmacología
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    Por favor, use este identificador para citar o enlazar este ítem:https://uvadoc.uva.es/handle/10324/72929

    Título
    Three-sectioning method: A procedure for studying hard tissues and large pieces under light and electron microscopy
    Autor
    Gayoso Del Villar, Jorge
    Garrosa García, ManuelAutoridad UVA Orcid
    Gayoso del Villar, Sara
    Rodríguez Arias, Carlos AlbertoAutoridad UVA
    Martín Ferrero, Miguel ÁngelAutoridad UVA Orcid
    Gayoso Rodríguez, Manuel JoséAutoridad UVA Orcid
    Año del Documento
    2020
    Editorial
    Elsevier
    Descripción
    Producción Científica
    Documento Fuente
    Micron. May 2020 ;Vol.132:102841: p.1-6
    Resumen
    The 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.
    Palabras Clave
    Hard Tissue, Prostheses, Plastic Enbedding, Epoxy resin, Sectioning, Bone, Nerve, Thick sections, Ultrathin sections, TEM, SEM.
    ISSN
    0968-4328
    Revisión por pares
    SI
    DOI
    10.1016/j.micron.2020.102841
    Patrocinador
    Este trabajo forma parte del proyecto de investigación financiado por la Junta de Castilla y León a través del Centro en Red de Medicina Regenerativa
    Version del Editor
    https://www.sciencedirect.com/science/article/pii/S0968432819303142
    Propietario de los Derechos
    Elsevier
    Idioma
    eng
    URI
    https://uvadoc.uva.es/handle/10324/72929
    Tipo de versión
    info:eu-repo/semantics/publishedVersion
    Derechos
    restrictedAccess
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    • DEP05 - Artículos de revista [198]
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    Universidad de Valladolid

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