Functionality of cryopreserved juvenile ovaries from mutant mice in different genetic background strains after allotransplantation

被引:4
作者
Huang, Kuo-Yu [1 ,2 ]
de Groot, Suzanna A. [1 ]
Woelders, Henri [3 ]
van der Horst, Gijsbertus T. J. [4 ]
Themmen, Axel P. N. [5 ]
Colenbrander, Ben [2 ]
van Vlissingen, J. Martje Fentener [1 ]
机构
[1] Erasmus Univ, Med Ctr, Erasmus Lab Anim Sci Ctr, NL-3000 CA Rotterdam, Netherlands
[2] Univ Utrecht, Fac Vet Med, Dept Farm Anim Hlth, NL-3508 TD Utrecht, Netherlands
[3] Univ Wageningen & Res Ctr, Anim Sci Grp, NL-8200 AB Lelystad, Netherlands
[4] Erasmus Univ, Med Ctr, Dept Genet, NL-3000 CA Rotterdam, Netherlands
[5] Erasmus Univ, Med Ctr, Dept Internal Med, NL-3000 CA Rotterdam, Netherlands
关键词
Mutant mouse; Ovary transplant; Cryopreservation; Ultra-rapid freezing; Fertility; IN-VITRO FERTILIZATION; ADULT-MOUSE OVARIES; DNA-REPAIR ENZYME; ORTHOTOPIC TRANSPLANTATION; ANTRAL FOLLICLES; TISSUE; VITRIFICATION; OOCYTES; FERTILITY; PROTEIN;
D O I
10.1016/j.cryobiol.2009.10.003
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The rapid expansion of mutant mouse colonies for biomedical research has resulted in lack of space at laboratory animal facilities and increasing risks of losing precious lines These challenges require cheap and effective methods in addition to freezing embryos and sperm to archive the expanding Mutant mouse lines Cryopreservation of mouse ovarian tissue has been reported, but the application in the diverse mutant lines and genetic backgrounds has not yet been studied In this Study, Juvenile ovaries (10-day-old) collected from genetically modified mouse lines were cryopreserved using high concentrations of cryoprotectants (dimethyl sulfoxide (Me2SO) and ethylene glycol (EG)) and instrumented ultra-rapid freezing The validation of the frozen ovary batches was assessed by orthotopically transplanting a thawed ovary into a nearly completely ovariectomized mature female (congenic with the ovary donor) After 2 weeks of recovery, the ovary recipient Was Continuously paired with a male (congenic with the ovary donor) to evaluate the fertility of the recipient and delivered offspring were genotyped to evaluate the continued functionality of the grafted ovary The recipient females delivered genetically modified offspring starting 6 weeks after ovary transplantation and lasting up to 6 months The presented cryopreservation and transplantation protocols enabled retrieval of the genetic modification in 20 (from 22) genetically modified mutant mouse models on a C57BL/6 (17). FVB (2), or BALB/c (1) background The thawed ovaries functioned after successful orthotopic allotransplantation to congenic wild-type recipients and produced mutant offspring, which allowed recreation of the desired genotype as a heterozygote oil the proper genetic background The results indicate that cryopreservation of mouse ovaries is a promising method to preserve genetic modification of the increasing number Of Mutant mouse models and call be used as a model for ovary cryopreservation using a variety of mouse mutants (C) 2009 Elsevier Inc All rights reserved
引用
收藏
页码:129 / 137
页数:9
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