Cryopreservation of early stage Siberian sturgeon Acipenser baerii germ cells, comparison of whole tissue and dissociated cells
Language English Country Netherlands Media print-electronic
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
26920821
DOI
10.1016/j.cryobiol.2016.02.005
PII: S0011-2240(16)30008-6
Knihovny.cz E-resources
- Keywords
- Cryopreservation, Germ cells, Germ-line chimera, Oogonia, Spermatogonia, Sturgeon,
- MeSH
- Dimethyl Sulfoxide pharmacology MeSH
- Ethylene Glycol pharmacology MeSH
- Glycerol pharmacology MeSH
- Cryopreservation methods MeSH
- Cryoprotective Agents pharmacology MeSH
- Endangered Species MeSH
- Organ Culture Techniques MeSH
- Ovum cytology drug effects transplantation MeSH
- Cell Proliferation drug effects MeSH
- Propylene Glycol pharmacology MeSH
- Fishes physiology MeSH
- Spermatozoa cytology drug effects transplantation MeSH
- Cell Survival drug effects MeSH
- Freezing MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Dimethyl Sulfoxide MeSH
- Ethylene Glycol MeSH
- Glycerol MeSH
- Cryoprotective Agents MeSH
- Propylene Glycol MeSH
Several sturgeon species are near extinction; therefore an efficient conservation strategy is required. Germ stem cells can be used for long-term storage and restoration of genetic information using surrogate reproduction. This study compared cryopreservation procedures of early stages of Siberian sturgeon Acipenser baerii testicular and ovarian cells. Whole gonad tissue or dissociated cells were frozen at a cooling rate of 1 °C/min in phosphate buffered saline with 0.5% bovine serum albumin, 50 mM glucose, and one of four different 1.5 M cryoprotectants: dimethyl sulfoxide, glycerol, ethylene glycol, or dimethyl sulfoxide with propanediol. The number of living cells obtained from 0.1 g of gonadal tissue after freeze/thaw of both whole tissue and dissociated cells was higher using ethylene glycol than with other cryoprotectants. Although there were no differences in the number of living cells in cryopreserved whole tissue vs. dissociated cells, the number of dead cells was lower with whole tissue cryopreservation, indicating that cells that died during freeze/thaw were digested during subsequent enzymatic dissociation. This resulted in more than 90% live cells after freeze/thaw and dissociation. The thawed tissue cryopreserved using ethylene glycol as protectant as well as fresh gonadal tissue were dissociated, and the cells were labelled by PKH26 and transplanted into larvae of sterlet Acipenser ruthenus. Ninety days post-transplant of both fresh and cryopreserved cells, introduced cells proliferated in more than half of the recipients.
References provided by Crossref.org
Delivery of Iron Oxide Nanoparticles into Primordial Germ Cells in Sturgeon
Cryopreservation and transplantation of common carp spermatogonia
Dnd1 Knockout in Sturgeons By CRISPR/Cas9 Generates Germ Cell Free Host for Surrogate Production
Elimination of primordial germ cells in sturgeon embryos by ultraviolet irradiation