Abstract
We have devised a cell culture system for Penaeus monodon prawn cells that uses a defined synthetic medium. Organs were removed from adult prawns ranging in size from 13-19 cm rostrum-to-telson length. Cultures consisted of either a blend of hematopoietic and lymphoid cells or ovarian cells. The cells divide rapidly in culture, doubling on average once per week for 5 to 6 weeks. These cultures continue to survive for at least 5 months but the rates of cell division are low after the first 5-6 weeks. In the literature, unicellular eukaryotic marine organisms such as chytrids may contaminate marine cell cultures. In some cases these eukaryotic contaminants may be difficult to distinguish from prawn cells unless detailed ultrastructure or characteristic developmental stages such as zoospores can be observed. Alternatively, we prepared molecular probes from repeated DNA sequences 100-400 bp in length in the P. monodon genome. These species-specific probes were hybridised to genomic DNA from cell culture to confirm proliferation of P. monodon cells in our cultures.
Original language | English (US) |
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Pages (from-to) | 219-223 |
Number of pages | 5 |
Journal | Methods in Cell Science |
Volume | 21 |
Issue number | 4 |
DOIs | |
State | Published - 1999 |
Externally published | Yes |
Keywords
- Cell culture
- In vitro
- Prawn tissues
ASJC Scopus subject areas
- Cell Biology