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Developments in marine invertebrate primary culture reveal novel cell morphologies in the model bivalve Crassostrea gigas
Cell culture provides useful model systems used in a wide range of biological applications, but its utility in marine invertebrates is limited due to the lack of immortalised cell lines. Primary cell and tissue cultures are typically used but remain poorly characterised for oysters, which can cause...
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Published in: | PeerJ (San Francisco, CA) CA), 2020-06, Vol.8, p.e9180, Article e9180 |
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description | Cell culture provides useful model systems used in a wide range of biological applications, but its utility in marine invertebrates is limited due to the lack of immortalised cell lines. Primary cell and tissue cultures are typically used but remain poorly characterised for oysters, which can cause issues with experimental consistency and reproducibility. Improvements to methods of repeatable isolation, culture, and characterisation of oyster cells and tissues are required to help address these issues. In the current study, systematic improvements have been developed to facilitate the culture of primary cells from adult Pacific oyster tissues and identify novel cell morphologies that have not been reported previously. Cultures analysed by light microscopy, qPCR, and live cell imaging demonstrated maintenance of live, metabolically active Pacific oyster cells for several weeks post-explant. Interestingly, whole hearts dissected from adult oysters were found to continue contracting rhythmically up to 8 weeks after being transferred to a tissue culture system. Mantle tissue explants were also actively moving in the culture system. These improvements in primary cell culture of bivalves may be beneficial for research in ecotoxicology, virology, immunology, and genetic resistance to disease. |
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Primary cell and tissue cultures are typically used but remain poorly characterised for oysters, which can cause issues with experimental consistency and reproducibility. Improvements to methods of repeatable isolation, culture, and characterisation of oyster cells and tissues are required to help address these issues. In the current study, systematic improvements have been developed to facilitate the culture of primary cells from adult Pacific oyster tissues and identify novel cell morphologies that have not been reported previously. Cultures analysed by light microscopy, qPCR, and live cell imaging demonstrated maintenance of live, metabolically active Pacific oyster cells for several weeks post-explant. Interestingly, whole hearts dissected from adult oysters were found to continue contracting rhythmically up to 8 weeks after being transferred to a tissue culture system. Mantle tissue explants were also actively moving in the culture system. These improvements in primary cell culture of bivalves may be beneficial for research in ecotoxicology, virology, immunology, and genetic resistance to disease.</description><identifier>ISSN: 2167-8359</identifier><identifier>EISSN: 2167-8359</identifier><identifier>DOI: 10.7717/peerj.9180</identifier><identifier>PMID: 32547861</identifier><language>eng</language><publisher>United States: PeerJ. Ltd</publisher><subject>Bivalvia ; Cell Biology ; Cell culture ; Cell lines ; Crassostrea gigas ; Disease resistance ; Diseases ; EDTA ; Environmental toxicology ; Explants ; Invertebrates ; Isolation ; Laboratories ; Light microscopy ; Live cell imaging ; Mantle ; Marine Biology ; Methods ; Microorganisms ; Microscopy ; Novels ; Oysters ; Pacific oyster ; Primary cell culture ; Seawater ; Senescence ; Tissue culture ; Tissue explant</subject><ispartof>PeerJ (San Francisco, CA), 2020-06, Vol.8, p.e9180, Article e9180</ispartof><rights>2020 Potts et al.</rights><rights>COPYRIGHT 2020 PeerJ. Ltd.</rights><rights>2020 Potts et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 Potts et al. 2020 Potts et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c570t-35bc39b6fb669feb5518dab64fee3ac791136233caa49a3d32f5be16ab10b24c3</citedby><cites>FETCH-LOGICAL-c570t-35bc39b6fb669feb5518dab64fee3ac791136233caa49a3d32f5be16ab10b24c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2408352034/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2408352034?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32547861$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Potts, Robert W A</creatorcontrib><creatorcontrib>Gutierrez, Alejandro P</creatorcontrib><creatorcontrib>Cortés-Araya, Yennifer</creatorcontrib><creatorcontrib>Houston, Ross D</creatorcontrib><creatorcontrib>Bean, Tim P</creatorcontrib><title>Developments in marine invertebrate primary culture reveal novel cell morphologies in the model bivalve Crassostrea gigas</title><title>PeerJ (San Francisco, CA)</title><addtitle>PeerJ</addtitle><description>Cell culture provides useful model systems used in a wide range of biological applications, but its utility in marine invertebrates is limited due to the lack of immortalised cell lines. Primary cell and tissue cultures are typically used but remain poorly characterised for oysters, which can cause issues with experimental consistency and reproducibility. Improvements to methods of repeatable isolation, culture, and characterisation of oyster cells and tissues are required to help address these issues. In the current study, systematic improvements have been developed to facilitate the culture of primary cells from adult Pacific oyster tissues and identify novel cell morphologies that have not been reported previously. Cultures analysed by light microscopy, qPCR, and live cell imaging demonstrated maintenance of live, metabolically active Pacific oyster cells for several weeks post-explant. Interestingly, whole hearts dissected from adult oysters were found to continue contracting rhythmically up to 8 weeks after being transferred to a tissue culture system. Mantle tissue explants were also actively moving in the culture system. These improvements in primary cell culture of bivalves may be beneficial for research in ecotoxicology, virology, immunology, and genetic resistance to disease.</description><subject>Bivalvia</subject><subject>Cell Biology</subject><subject>Cell culture</subject><subject>Cell lines</subject><subject>Crassostrea gigas</subject><subject>Disease resistance</subject><subject>Diseases</subject><subject>EDTA</subject><subject>Environmental toxicology</subject><subject>Explants</subject><subject>Invertebrates</subject><subject>Isolation</subject><subject>Laboratories</subject><subject>Light microscopy</subject><subject>Live cell imaging</subject><subject>Mantle</subject><subject>Marine Biology</subject><subject>Methods</subject><subject>Microorganisms</subject><subject>Microscopy</subject><subject>Novels</subject><subject>Oysters</subject><subject>Pacific oyster</subject><subject>Primary cell culture</subject><subject>Seawater</subject><subject>Senescence</subject><subject>Tissue culture</subject><subject>Tissue explant</subject><issn>2167-8359</issn><issn>2167-8359</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUl1r2zAUNWNjLV1f9gOGYbCHQTJLsiX7ZVCyrSsU9rI9iyv5ylGQrUySA_33VZOsTWDSgy7nnnPQ_SiK96RaCkHEly1i2Cw70laviktKuFi0rOlen8QXxXWMmyqflvKqZW-LC0abWrScXBYP33CHzm9HnFIs7VSOEOyEOdphSKgCJCy3wWb4odSzS3PAMmQNuHLyWVpqdK4cfdiuvfODxb1LWmPG-pxWdgduh-UqQIw-poBQDnaA-K54Y8BFvD6-V8WfH99_r34u7n_d3q1u7he6EVVasEZp1iluFOedQdU0pO1B8dogMtCiI4RxypgGqDtgPaOmUUg4KFIpWmt2VdwdfHsPG3ksRXqwcg_4MEgIyWqHkhnODbZQc1XVXatACF4haxhSarSC7PX14LWd1Yi9zk0L4M5MzzOTXcvB76SggrRdlQ0-Hg2C_ztjTHLj5zDl-iWt82waWrH6hTVA_pWdjM9merRRyxueR0c5EySzlv9h5dvjaLWf0NiMnwk-nQjWeYRpHb2bk_VTPCd-PhB18DEGNM8Vkko-bZ3cb5182rpM_nDak2fqvx1jj_Ij1NY</recordid><startdate>20200601</startdate><enddate>20200601</enddate><creator>Potts, Robert W A</creator><creator>Gutierrez, Alejandro P</creator><creator>Cortés-Araya, Yennifer</creator><creator>Houston, Ross D</creator><creator>Bean, Tim P</creator><general>PeerJ. 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Primary cell and tissue cultures are typically used but remain poorly characterised for oysters, which can cause issues with experimental consistency and reproducibility. Improvements to methods of repeatable isolation, culture, and characterisation of oyster cells and tissues are required to help address these issues. In the current study, systematic improvements have been developed to facilitate the culture of primary cells from adult Pacific oyster tissues and identify novel cell morphologies that have not been reported previously. Cultures analysed by light microscopy, qPCR, and live cell imaging demonstrated maintenance of live, metabolically active Pacific oyster cells for several weeks post-explant. Interestingly, whole hearts dissected from adult oysters were found to continue contracting rhythmically up to 8 weeks after being transferred to a tissue culture system. Mantle tissue explants were also actively moving in the culture system. These improvements in primary cell culture of bivalves may be beneficial for research in ecotoxicology, virology, immunology, and genetic resistance to disease.</abstract><cop>United States</cop><pub>PeerJ. Ltd</pub><pmid>32547861</pmid><doi>10.7717/peerj.9180</doi><oa>free_for_read</oa></addata></record> |
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subjects | Bivalvia Cell Biology Cell culture Cell lines Crassostrea gigas Disease resistance Diseases EDTA Environmental toxicology Explants Invertebrates Isolation Laboratories Light microscopy Live cell imaging Mantle Marine Biology Methods Microorganisms Microscopy Novels Oysters Pacific oyster Primary cell culture Seawater Senescence Tissue culture Tissue explant |
title | Developments in marine invertebrate primary culture reveal novel cell morphologies in the model bivalve Crassostrea gigas |
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