Chill sensitivity and cryoprotectant permeability of dechorionated zebrafish embryos, Brachydanio rerio

被引:92
作者
Hagedorn, M
Kleinhans, FW
Wildt, DE
Rall, WF
机构
[1] SMITHSONIAN INST, CONSERVAT & RES CTR, WASHINGTON, DC 20008 USA
[2] INDIANA UNIV PURDUE UNIV, DEPT PHYS, INDIANAPOLIS, IN 46202 USA
[3] NIH, VET RESOURCES PROGRAM, NATL CTR RES RESOURCES, BETHESDA, MD 20892 USA
关键词
D O I
10.1006/cryo.1997.2002
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The zebrafish (Brachydanio rerio) was used as a model for basic studies of the chilling sensitivity, permeability and toxicity of cryoprotectants. In both intact and dechorionated embryos, early stage embryos (1.25, 1.5, 1.75, and 2 h) were more susceptible (P < 0.05) to chilling injury at 0 degrees C than late-stage embryos (50, 75, and 100% epiboly and three-somite stage). Moreover, enzymatic removal of the chorion did not alter (P > 0.05) this pattern of sensitivity to chilling. Eight-hour zebrafish embryos tolerated short-term exposures to temperatures ranging from 4 to 23 degrees C for 3.5 h with no detrimental developmental effects. The permeability of dechorionated embryos to cryoprotectants was examined by measuring the kinetics of volumetric change at various develop mental stages (16 cells to six somites or ca 1.25 to 14 h postfertilization) at 28.5 degrees C. The dechorionated zebrafish embryo is composed of two complex cellular compartments (i.e., a large yolk and the developing blastoderm). From 40 to 100% epiboly, the volumes of the yolk and blastoderm remained constant, ca 82 and 18%, respectively. However, these volumes changed rapidly after epiboly. For example, at the six-somite stage, the yolk composed 61% of the total volume, whereas the blastoderm composed 39%. When three- and six-somite embryos were placed in 1.5 and 2.0 M cryoprotectants (dimethyl sulfoxide and propylene glycol), osmometric measurement of volume changes indicated no permeation of the cryoprotectants. However, some permeation was observed for six-somite embryos immersed in a 2.0 M methanol solution, but not for 3-somite embryos. For up to 30 min at room temperature, these cryoprotectant solutions were not toxic to zebrafish embryos; however, 1.5 M glycerol and ethylene glycol solutions were. We conclude that the complex nature of the zebrafish embryo reduces the effectiveness and predictive value of light microscopical measurements for cryoprotectant permeability studies. (C) 1997 Academic Press.
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页码:251 / 263
页数:13
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