Establishment and characterisation of single cell-derived embryonic stem cell lines from the gilthead seabream, Sparus aurata

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URI: http://hdl.handle.net/10498/24934
DOI: 10.1016/j.cbpb.2021.110626
ISSN: 1096-4959
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2021-05Department
Biología; Biomedicina, Biotecnología y Salud PúblicaSource
Comparative Biochemistry and Physiology, Part B 256 (2021) 110626Abstract
An important bottleneck in fish aquaculture research is the supply and maintenance of embryos, larvae, juvenile
and adult specimens. In this context, cell lines represent alternative experimental models for in vitro studies that
complement in vivo assays. This allows us to perform easier experimental design and sampling and avoid the
sacrifice of animals. Embryonic stem (ES) cell lines have attracted increasing attention because they have the
capability to proliferate indefinitely and could be differentiated into any cell type of the organism. To minimise
cell heterogeneity and increase uniformity of in vitro studies results, in this manuscript we report the development
and characterisation of two single cell-derived ES cell lines (monoclonal) from the morula stage embryos of
the gilthead seabream, Sparus aurata, named as SAEC-A3 and SAEC-H7. Both cell lines have been passaged for
over 100 times, indicating the establishment of long-term, immortalised ES cell cultures. Sequence analyses
confirmed the seabream origin of the cell lines, and growth analyses evidenced their high viability and proliferating
activity, particularly in culture medium supplemented with 10–15% fetal bovine serum and 22 ◦C. Both
cell lines showed the ability to generate embryoid bodies and show different sensitivity and response to all-trans
retinoic acid. The analysis of epithelial (col1α1) and neuronal (sox3) markers in differentiated cultures revealed
that SAEC-A3 tended to differentiate towards epithelial-like cells whereas SAEC-H7 tended to differentiate towards
neuronal-like cells. Both cell lines were efficiently transfected with pDsRed2-ER and/or pEGFP-N1 plasmids,
indicating that they could represent useful biotechnological tools. Daily expression of pcna showed
significant expression rhythms, with maximum levels of cell proliferation during the day-night transition.
Currently, these cell lines are being successfully used as experimental models for the study of cellular metabolism,
physiology and rhythms as well as for toxicological, pharmacological and gene expression analyses.
Subjects
Embryonic stem cell lines; Monoclonal cell line; pcna; In vitro studies; Sparus aurata; Embryoid bodies; AquacultureCollections
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