Cargando…

Application of the mirror technique for block-face scanning electron microscopy

The mirror technique adapted for electron microscopy allows correlating neuronal structures across the cutting plane of adjoining light microscopic sections which, however, have a limited thickness, typically less than 100 µm (Talapka et al. in Front Neuroanat, 2021, 10.3389/fnana.2021.652422). Here...

Descripción completa

Detalles Bibliográficos
Autores principales: Talapka, Petra, Bába, Bence Béla, Mészár, Zoltán, Kisvárday, Réka Eszter, Kocsis, Zsolt, Srivastava, Mohit, Kisvárday, Zoltán
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232443/
https://www.ncbi.nlm.nih.gov/pubmed/35643821
http://dx.doi.org/10.1007/s00429-022-02506-w
Descripción
Sumario:The mirror technique adapted for electron microscopy allows correlating neuronal structures across the cutting plane of adjoining light microscopic sections which, however, have a limited thickness, typically less than 100 µm (Talapka et al. in Front Neuroanat, 2021, 10.3389/fnana.2021.652422). Here, we extend the mirror technique for tissue blocks in the millimeter range and demonstrate compatibility with serial block-face electron microscopy (SBEM). An essential step of the methodological improvement regards the recognition that unbound resin must be removed from the tissue surface to gain visibility of surface structures. To this, the tissue block was placed on absorbent paper during the curing process. In this way, neuronal cell bodies could be unequivocally identified using epi-illumination and confocal microscopy. Thus, the layout of cell bodies which were cut by the sectioning plane can be correlated with the layout of their complementary part in the adjoining section processed for immunohistochemistry. The modified mirror technique obviates the spatial limit in investigating synaptology of neurochemically identified structures such as neuronal processes, dendrites and axons. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00429-022-02506-w.