PUBLICATION

Vitrification of caudal fin explants from zebrafish adult specimens

Authors
Cardona-Costa, J., Roig, J., Perez-Camps, M., and Garcia-Ximenez, F.
ID
ZDB-PUB-070210-38
Date
2006
Source
Cryo letters   27(5): 329-332 (Journal)
Registered Authors
Cardona-Costa, Jose
Keywords
Cryopreservation, vitrification, cryoprotectants, zebrafish, tissue culture, biodiversity
MeSH Terms
  • Animals
  • Cryopreservation/methods*
  • Cryoprotective Agents/pharmacology
  • Cryoprotective Agents/standards
  • Dimethyl Sulfoxide/pharmacology
  • Drug Combinations
  • Ethylene Glycol/pharmacology
  • Methanol/pharmacology
  • Organ Culture Techniques
  • Propylene Glycol/pharmacology
  • Zebrafish*
PubMed
17256066
Abstract
No data on vitrification of tissue samples are available in fishes. Three vitrification solutions were compared: V1: 20% ethylene glycol and 20% dimethyl sulphoxide; V2: 25% propylene glycol and 20% dimethyl sulphoxide, and; V3: 20% propylene glycol and 13% methanol, all three prepared in Hanks' buffered salt solution plus 20 percent FBS, following the same one step vitrification procedure developed in mammals. Caudal fin tissue pieces were vitrified into 0.25 ml plastic straws in 30s and stored in liquid nitrogen for 3 days minimum, warmed (10s in nitrogen vapour and 5s in a 25 degree C water bath) and cultured (L-15 plus 20% FBS at 28.5 degree C). At the third day of culture, both attachment and outgrowing rates were recorded. V3 led to the worst results (8% of attachment rate). V1 and V2 allow higher attachment rates (V1: 63% vs V2: 50%. P < 0.05) but not significantly different outgrowing rates (83% to 94%). Vitrification of caudal fin pieces is advantageous in fish biodiversity conservation, particularly in the wild, due to the simplicity of procedure and equipment.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping