5
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Developments in marine invertebrate primary culture reveal novel cell morphologies in the model bivalve Crassostrea gigas

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          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.

          Related collections

          Most cited references39

          • Record: found
          • Abstract: found
          • Article: not found

          Cellular senescence in human myoblasts is overcome by human telomerase reverse transcriptase and cyclin-dependent kinase 4: consequences in aging muscle and therapeutic strategies for muscular dystrophies.

          Cultured human myoblasts fail to immortalize following the introduction of telomerase. The availability of an immortalization protocol for normal human myoblasts would allow one to isolate cellular models from various neuromuscular diseases, thus opening the possibility to develop and test novel therapeutic strategies. The parameters limiting the efficacy of myoblast transfer therapy (MTT) could be assessed in such models. Finally, the presence of an unlimited number of cell divisions, and thus the ability to clone cells after experimental manipulations, reduces the risks of insertional mutagenesis by many orders of magnitude. This opportunity for genetic modification provides an approach for creating a universal donor that has been altered to be more therapeutically useful than its normal counterpart. It can be engineered to function under conditions of chronic damage (which are very different than the massive regeneration conditions that recapitulate normal development), and to overcome the biological problems such as cell death and failure to proliferate and migrate that limit current MTT strategies. We describe here the production and characterization of a human myogenic cell line, LHCN-M2, that has overcome replicative aging due to the expression of telomerase and cyclin-dependent kinase 4. We demonstrate that it functions as well as young myoblasts in xenotransplant experiments in immunocompromized mice under conditions of regeneration following muscle damage.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Properties of a clonal muscle cell line from rat heart.

              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              A New Critical Estimate of Named Species-Level Diversity of the Recent Mollusca*

                Bookmark

                Author and article information

                Contributors
                Journal
                PeerJ
                PeerJ
                peerj
                peerj
                PeerJ
                PeerJ Inc. (San Diego, USA )
                2167-8359
                1 June 2020
                2020
                : 8
                : e9180
                Affiliations
                [1 ]The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh , Edinburgh, United Kingdom
                [2 ]Centre for Environment Fisheries and Aquaculture Science (Cefas) Weymouth Laboratory , Dorset, United Kingdom
                Article
                9180
                10.7717/peerj.9180
                7271890
                32547861
                6c8603d5-16f3-48f1-b529-d70e33655191
                ©2020 Potts et al.

                This is an open access article distributed under the terms of the Creative Commons Attribution 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.

                History
                : 15 January 2020
                : 22 April 2020
                Funding
                Funded by: Biotechnology and Biological Sciences Research Council (BBSRC)
                Award ID: BB/M010996/1
                Funded by: BBSRC Institute Strategic Programme Grants
                Award ID: BBS/E/D/20002172
                Award ID: BBS/E/D/30002275
                Funded by: Centre for Environment, Fisheries and Aquaculture Science (Cefas) Seedcorn
                Award ID: DP901W
                This work was supported by the Biotechnology and Biological Sciences Research Council (BBSRC) (grant number BB/M010996/1), BBSRC Institute Strategic Programme Grants (BBS/E/D/20002172 and BBS/E/D/30002275) and Centre for Environment, Fisheries and Aquaculture Science (Cefas) Seedcorn project DP901W. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Cell Biology
                Marine Biology

                primary cell culture,pacific oyster,tissue explant,live cell imaging

                Comments

                Comment on this article