4.1 Article

Assessment of three generations of mice derived by ICSI using freeze-dried sperm

期刊

ZYGOTE
卷 17, 期 3, 页码 239-251

出版社

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0967199409005292

关键词

Freeze drying; ICSI; Microsatellite; Mouse; Sperm

资金

  1. National Institute of Child Health and Human Development [U01 HD38205]
  2. National Center for Research Resources [U01 HD38228]
  3. NIH/NCRR U42 [RR014905]
  4. UC Davis Mouse Biology Program
  5. National Center for Research Resources (NCRR) [UL1 RR024146]
  6. National Institutes of Health (NIH)
  7. NIH Roadmap for Medical Research

向作者/读者索取更多资源

Although the derivation of mice by intracytoplasmic sperm injection (ICSI) using freeze-dried sperm has been demonstrated previously, a comprehensive analysis of their viability, health, and fertility has not. The purpose of the present study was to determine the extent to which ICSI using freeze-dried sperm stored at 4 degrees C for 1-2 months from mice on either an inbred (C57BL/6J) or hybrid (B6D2F1/J) genetic background results in genomic instability and/or phenotypic abnormality in mice and two generations of their progeny. Fertilization rates (number of 2-cells per injected oocytes) using ICSI of fresh and freeze-dried sperm were similar within and between mouse strains, although fewer freeze-dried sperm-derived embryos than fresh sperm-derived embryos developed to blastocysts in vitro (C57BL/6J and B6D2F1/J) and liveborn pups in vivo (B6D2F1/J only). Nevertheless, once born, mice derived by ICSI using freeze-dried sperm in both mouse strains were healthy and reproductively Sound. No major differences in litter size, weaning rate, and sex ratio were noted in the two generations of progeny (F2 and F3) of ICSI-derived offspring using freeze-dried sperm compared with that in the natural mating (control) group. Further, there was no evidence that either ICSI or freeze drying induced genomic instability, as determined by microsatellite analysis of the derived mice and Subsequent generations when compared with both parental genotypes, nor were there differences in the number or types of pathological changes in any of the three generations of progeny. We conclude that viable, healthy and genomically stable mice can be derived by ICSI using freeze-dried mouse sperm stored in the refrigerator for at least 2 months. Further, because freeze drying is a simpler and more economical technique compared with embryo and sperm cryopreservation, the results of this study justify additional research to continue to develop and enhance the technique for the preservation, storage, and sharing of genetically altered mice.

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