ZFIN ID: ZDB-PUB-041111-9
Developmental expression of aquaporin-3 in zebrafish embryos (Danio rerio)
Lance, S.L., Peterson, A.S., and Hagedorn, M.
Date: 2004
Source: Comparative biochemistry and physiology. Toxicology & pharmacology : CBP 138(3): 251-258 (Journal)
Registered Authors: Hagedorn, Mary
Keywords: Cryobiology; Cryopreservation; Teleost fish; Embryos; Zebrafish; Water permeability; Cryoprotectant permeability; Aquaporins
MeSH Terms:
  • Animals
  • Aquaporin 3
  • Aquaporins/metabolism*
  • Culture Media
  • Embryo, Nonmammalian/drug effects
  • Embryo, Nonmammalian/embryology
  • Embryo, Nonmammalian/metabolism
  • Gene Expression Regulation, Developmental*/drug effects
  • Microscopy, Confocal
  • Osmolar Concentration
  • Sodium Chloride/pharmacology
  • Sucrose/pharmacology
  • Survival Rate
  • Zebrafish/embryology*
  • Zebrafish/metabolism*
PubMed: 15533783 Full text @ Comp. Biochem. Physiol. C Toxicol. Pharmacol.
Fish embryos have never been successfully cryopreserved because of the low permeability of cryoprotectants into the yolk. Recently, we used aquaporin-3 fused with a green fluorescent protein (AQP3GFP) to modify the zebrafish embryo, and demonstrated that the pores functioned physiologically. This increased the water and cryoprotectant permeability of the membranes. We have continued our work on AQP3-modified embryos and here we report their developmental expression of AQP3, the success of various culture media on their survival and development, and their reproductive success. The AQP3GFP expression begins within 30 m after the mRNA AQP3GFP injection into the yolk of the 1- to 4-cell embryo. This expression is distributed in the membranes throughout the blastoderm and the yolk syncytial layer within 24 h. It diminishes after 96 h. We found no difference in the survival or normal development of embryos from AQP3GFP or wild-type adults. Additionally, zebrafish embryos did not require special culture medium to survive after AQP3GFP modification. In fact, they survived best in embryo medium (ca. 40 mOsm). Embryos reared entirely in embryo medium had a higher percent survival and a higher percent normal development than those exposed to a high osmolality sucrose culture medium (ca. 330 mOsm). The mechanism whereby these embryos can maintain their internal osmolality in a hypoosmotic solution with water channels in their membranes is unknown.