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Scanning electron microscopy of murine skin ultrathin sections and cultured keratinocytes

Generating high-quality electron microscopy images of the skin and keratinocytes can be challenging. Here we describe a simple protocol for scanning electron microscopy (SEM) of murine skin. The protocol enables characterization of the ultrastructure of the epidermis, dermis, hair follicles, basemen...

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Detalles Bibliográficos
Autores principales: Banerjee, Avinanda, Biswas, Ritusree, Lim, Ryan, Pasolli, Hilda Amalia, Raghavan, Srikala
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379523/
https://www.ncbi.nlm.nih.gov/pubmed/34458866
http://dx.doi.org/10.1016/j.xpro.2021.100729
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author Banerjee, Avinanda
Biswas, Ritusree
Lim, Ryan
Pasolli, Hilda Amalia
Raghavan, Srikala
author_facet Banerjee, Avinanda
Biswas, Ritusree
Lim, Ryan
Pasolli, Hilda Amalia
Raghavan, Srikala
author_sort Banerjee, Avinanda
collection PubMed
description Generating high-quality electron microscopy images of the skin and keratinocytes can be challenging. Here we describe a simple protocol for scanning electron microscopy (SEM) of murine skin. The protocol enables characterization of the ultrastructure of the epidermis, dermis, hair follicles, basement membrane, and cell-cell junctions. We detail the specific steps for sample preparation and highlight the critical need for proper orientation of the sample for ultrathin sectioning. We also describe the isolation and preparation of primary keratinocyte monolayers for SEM. For complete details on the use and execution of this protocol, please refer to Biswas et al. (2021).
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spelling pubmed-83795232021-08-27 Scanning electron microscopy of murine skin ultrathin sections and cultured keratinocytes Banerjee, Avinanda Biswas, Ritusree Lim, Ryan Pasolli, Hilda Amalia Raghavan, Srikala STAR Protoc Protocol Generating high-quality electron microscopy images of the skin and keratinocytes can be challenging. Here we describe a simple protocol for scanning electron microscopy (SEM) of murine skin. The protocol enables characterization of the ultrastructure of the epidermis, dermis, hair follicles, basement membrane, and cell-cell junctions. We detail the specific steps for sample preparation and highlight the critical need for proper orientation of the sample for ultrathin sectioning. We also describe the isolation and preparation of primary keratinocyte monolayers for SEM. For complete details on the use and execution of this protocol, please refer to Biswas et al. (2021). Elsevier 2021-08-17 /pmc/articles/PMC8379523/ /pubmed/34458866 http://dx.doi.org/10.1016/j.xpro.2021.100729 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Banerjee, Avinanda
Biswas, Ritusree
Lim, Ryan
Pasolli, Hilda Amalia
Raghavan, Srikala
Scanning electron microscopy of murine skin ultrathin sections and cultured keratinocytes
title Scanning electron microscopy of murine skin ultrathin sections and cultured keratinocytes
title_full Scanning electron microscopy of murine skin ultrathin sections and cultured keratinocytes
title_fullStr Scanning electron microscopy of murine skin ultrathin sections and cultured keratinocytes
title_full_unstemmed Scanning electron microscopy of murine skin ultrathin sections and cultured keratinocytes
title_short Scanning electron microscopy of murine skin ultrathin sections and cultured keratinocytes
title_sort scanning electron microscopy of murine skin ultrathin sections and cultured keratinocytes
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379523/
https://www.ncbi.nlm.nih.gov/pubmed/34458866
http://dx.doi.org/10.1016/j.xpro.2021.100729
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