Novel methods to establish whole-body primary cell cultures for the cnidarians Nematostella vectensis and Pocillopora damicornis
Abstract Cnidarians are emerging model organisms for cell and molecular biology research. However, successful cell culture development has been challenging due to incomplete tissue dissociation and contamination. In this report, we developed and tested several different methodologies to culture prim...
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2021-02-01
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Online Access: | https://doi.org/10.1038/s41598-021-83549-7 |
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doaj-175cdaa83688460c8babaf0723585c9c2021-02-21T12:33:20ZengNature Publishing GroupScientific Reports2045-23222021-02-011111910.1038/s41598-021-83549-7Novel methods to establish whole-body primary cell cultures for the cnidarians Nematostella vectensis and Pocillopora damicornisJames D. Nowotny0Michael T. Connelly1Nikki Traylor-Knowles2Rosenstiel School of Marine and Atmospheric Science, University of MiamiRosenstiel School of Marine and Atmospheric Science, University of MiamiRosenstiel School of Marine and Atmospheric Science, University of MiamiAbstract Cnidarians are emerging model organisms for cell and molecular biology research. However, successful cell culture development has been challenging due to incomplete tissue dissociation and contamination. In this report, we developed and tested several different methodologies to culture primary cells from all tissues of two species of Cnidaria: Nematostella vectensis and Pocillopora damicornis. In over 170 replicated cell cultures, we demonstrate that physical dissociation was the most successful method for viable and diverse N. vectensis cells while antibiotic-assisted dissociation was most successful for viable and diverse P. damicornis cells. We also demonstrate that a rigorous antibiotic pretreatment results in less initial contamination in cell cultures. Primary cultures of both species averaged 12–13 days of viability, showed proliferation, and maintained high cell diversity including cnidocytes, nematosomes, putative gastrodermal, and epidermal cells. Overall, this work will contribute a needed tool for furthering functional cell biology experiments in Cnidaria.https://doi.org/10.1038/s41598-021-83549-7 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
James D. Nowotny Michael T. Connelly Nikki Traylor-Knowles |
spellingShingle |
James D. Nowotny Michael T. Connelly Nikki Traylor-Knowles Novel methods to establish whole-body primary cell cultures for the cnidarians Nematostella vectensis and Pocillopora damicornis Scientific Reports |
author_facet |
James D. Nowotny Michael T. Connelly Nikki Traylor-Knowles |
author_sort |
James D. Nowotny |
title |
Novel methods to establish whole-body primary cell cultures for the cnidarians Nematostella vectensis and Pocillopora damicornis |
title_short |
Novel methods to establish whole-body primary cell cultures for the cnidarians Nematostella vectensis and Pocillopora damicornis |
title_full |
Novel methods to establish whole-body primary cell cultures for the cnidarians Nematostella vectensis and Pocillopora damicornis |
title_fullStr |
Novel methods to establish whole-body primary cell cultures for the cnidarians Nematostella vectensis and Pocillopora damicornis |
title_full_unstemmed |
Novel methods to establish whole-body primary cell cultures for the cnidarians Nematostella vectensis and Pocillopora damicornis |
title_sort |
novel methods to establish whole-body primary cell cultures for the cnidarians nematostella vectensis and pocillopora damicornis |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-02-01 |
description |
Abstract Cnidarians are emerging model organisms for cell and molecular biology research. However, successful cell culture development has been challenging due to incomplete tissue dissociation and contamination. In this report, we developed and tested several different methodologies to culture primary cells from all tissues of two species of Cnidaria: Nematostella vectensis and Pocillopora damicornis. In over 170 replicated cell cultures, we demonstrate that physical dissociation was the most successful method for viable and diverse N. vectensis cells while antibiotic-assisted dissociation was most successful for viable and diverse P. damicornis cells. We also demonstrate that a rigorous antibiotic pretreatment results in less initial contamination in cell cultures. Primary cultures of both species averaged 12–13 days of viability, showed proliferation, and maintained high cell diversity including cnidocytes, nematosomes, putative gastrodermal, and epidermal cells. Overall, this work will contribute a needed tool for furthering functional cell biology experiments in Cnidaria. |
url |
https://doi.org/10.1038/s41598-021-83549-7 |
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