Short-term storage of sterlet Acipenser ruthenus testicular cells at -80 °C
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
26964775
DOI
10.1016/j.cryobiol.2016.03.002
PII: S0011-2240(16)30013-X
Knihovny.cz E-resources
- Keywords
- Aciperserids, Cryopreservation, Germ cells, Sterlet,
- MeSH
- Ethylene Glycol pharmacology MeSH
- Cryopreservation methods MeSH
- Cryoprotective Agents pharmacology MeSH
- Endangered Species MeSH
- Fishes * MeSH
- Temperature MeSH
- Testis cytology MeSH
- Organ Preservation methods MeSH
- Cell Survival MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Ethylene Glycol MeSH
- Cryoprotective Agents MeSH
The conservation of sturgeons is of critical importance, and optimization of long-term storage is crucial to cell survival. This study aimed to examine the viability rates of several variations of sturgeon testicular cells storage at -80 °C for purpose of a short-term storage in a deep freezer or shipment on dried ice. Testes extracted from three immature fish were cut into small pieces, immersed in a cryomedium composed of phosphate buffered saline with 0.5% bovine serum albumin, 50 mM glucose, and 1.5 M ethylene glycol as a cryoprotectant, chilled from 10 to -80 °C at a cooling rate of 1 °C per min, and stored under varying conditions. Our results revealed a significant effect of storage conditions on the number of living and dead cells (p > 0.05). Samples that were stored for 7 days at -80 °C showed a considerable decline in terms of cell viability compared to samples stored for 2 days storage at -80 °C or in LN. This result indicated that testicular cells can be stored at -80 °C and/or on dry ice, for 2 days with minimum loss of viability.
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