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Establishment of long-term ostracod epidermal culture
Primary crustacean cell culture was introduced in the 1960s, but to date limited cell lines have been established. Skogsbergia lerneri is a myodocopid ostracod, which has a body enclosed within a thin, durable, transparent bivalved carapace, through which the eye can see. The epidermal layer lines t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658072/ https://www.ncbi.nlm.nih.gov/pubmed/33034828 http://dx.doi.org/10.1007/s11626-020-00508-8 |
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author | Morgan, Siân R. Paletto, Laura Rumney, Benjamin Malik, Farhana T. White, Nick Lewis, Philip N. Parker, Andrew R. Holden, Simon Meek, Keith M. Albon, Julie |
author_facet | Morgan, Siân R. Paletto, Laura Rumney, Benjamin Malik, Farhana T. White, Nick Lewis, Philip N. Parker, Andrew R. Holden, Simon Meek, Keith M. Albon, Julie |
author_sort | Morgan, Siân R. |
collection | PubMed |
description | Primary crustacean cell culture was introduced in the 1960s, but to date limited cell lines have been established. Skogsbergia lerneri is a myodocopid ostracod, which has a body enclosed within a thin, durable, transparent bivalved carapace, through which the eye can see. The epidermal layer lines the inner surface of the carapace and is responsible for carapace synthesis. The purpose of the present study was to develop an in vitro epidermal tissue and cell culture method for S. lerneri. First, an optimal environment for the viability of this epidermal tissue was ascertained, while maintaining its cell proliferative capacity. Next, a microdissection technique to remove the epidermal layer for explant culture was established and finally, a cell dissociation method for epidermal cell culture was determined. Maintenance of sterility, cell viability and proliferation were key throughout these processes. This novel approach for viable S. lerneri epidermal tissue and cell culture augments our understanding of crustacean cell biology and the complex biosynthesis of the ostracod carapace. In addition, these techniques have great potential in the fields of biomaterial manufacture, the military and fisheries, for example, in vitro toxicity testing. |
format | Online Article Text |
id | pubmed-7658072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-76580722020-11-12 Establishment of long-term ostracod epidermal culture Morgan, Siân R. Paletto, Laura Rumney, Benjamin Malik, Farhana T. White, Nick Lewis, Philip N. Parker, Andrew R. Holden, Simon Meek, Keith M. Albon, Julie In Vitro Cell Dev Biol Anim Article Primary crustacean cell culture was introduced in the 1960s, but to date limited cell lines have been established. Skogsbergia lerneri is a myodocopid ostracod, which has a body enclosed within a thin, durable, transparent bivalved carapace, through which the eye can see. The epidermal layer lines the inner surface of the carapace and is responsible for carapace synthesis. The purpose of the present study was to develop an in vitro epidermal tissue and cell culture method for S. lerneri. First, an optimal environment for the viability of this epidermal tissue was ascertained, while maintaining its cell proliferative capacity. Next, a microdissection technique to remove the epidermal layer for explant culture was established and finally, a cell dissociation method for epidermal cell culture was determined. Maintenance of sterility, cell viability and proliferation were key throughout these processes. This novel approach for viable S. lerneri epidermal tissue and cell culture augments our understanding of crustacean cell biology and the complex biosynthesis of the ostracod carapace. In addition, these techniques have great potential in the fields of biomaterial manufacture, the military and fisheries, for example, in vitro toxicity testing. Springer US 2020-10-09 2020 /pmc/articles/PMC7658072/ /pubmed/33034828 http://dx.doi.org/10.1007/s11626-020-00508-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Morgan, Siân R. Paletto, Laura Rumney, Benjamin Malik, Farhana T. White, Nick Lewis, Philip N. Parker, Andrew R. Holden, Simon Meek, Keith M. Albon, Julie Establishment of long-term ostracod epidermal culture |
title | Establishment of long-term ostracod epidermal culture |
title_full | Establishment of long-term ostracod epidermal culture |
title_fullStr | Establishment of long-term ostracod epidermal culture |
title_full_unstemmed | Establishment of long-term ostracod epidermal culture |
title_short | Establishment of long-term ostracod epidermal culture |
title_sort | establishment of long-term ostracod epidermal culture |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658072/ https://www.ncbi.nlm.nih.gov/pubmed/33034828 http://dx.doi.org/10.1007/s11626-020-00508-8 |
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