Literature DB >> 12297546

Intracytoplasmic sperm injection is more efficient than in vitro fertilization for generating mouse embryos from cryopreserved spermatozoa.

Monika A Szczygiel1, Hirokazu Kusakabe, Ryuzo Yanagimachi, David G Whittingham.   

Abstract

Efficient and dependable mouse cryopreservation methods are urgently needed because the production of mice with transgenes and disrupted and mutant genes is now commonplace. Preservation of these unique genomes provides an essential safeguard for future research. Unfortunately, mouse spermatozoa appear more vulnerable to freezing than other species, e.g., bovine and human. In this study, we examined the efficiency of intracytoplasmic sperm injection (ICSI) and in vitro fertilization (IVF) in generating embryos from mouse spermatozoa frozen with 18% raffinose and 3% skim milk for cryoprotection. A comparison was made between the inbred strain C57BL/6J, commonly used in mutagenic and transgenic studies, and a hybrid strain B6D2F1 (C57BL/6J x DBA/2J). C57BL/6J spermatozoa are known to be more sensitive to freezing than B6D2F1. Fertilization of oocytes after IVF was significantly lower with C57BL/6J spermatozoa when compared with B6D2F1 spermatozoa for both fresh and frozen spermatozoa (fresh, 89 vs. 55%; frozen, 56 vs. 9%). Freezing also reduced the fertility of B6D2F1 spermatozoa (89 vs. 56%). Fertilization improved dramatically after ICSI with fresh and frozen C57BL/6J spermatozoa (90 and 85%) and also with frozen B6D2F1 spermatozoa (87%). The development of two-cell embryos to the blastocyst stage was lower for C57BL/6J than B6D2F1 (42-61% and 84-98%) in all treatments but similar for embryos within each strain. The normality of chromosomes from fresh and frozen spermatozoa was assessed in oocytes prior to first cleavage. The majority of oocytes had normal chromosomes after IVF (98-100%) and ICSI (87-95%), indicating that chromosomal abnormalities were not responsible for the poorer development in vitro of C57BL/6J embryos. In conclusion, our data show that ICSI is a more efficient and effective technique than IVF for generating embryos from frozen spermatozoa. More important, ICSI is especially valuable for strains where IVF with fresh spermatozoa produces few or no embryos.

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Year:  2002        PMID: 12297546     DOI: 10.1095/biolreprod67.4.1278

Source DB:  PubMed          Journal:  Biol Reprod        ISSN: 0006-3363            Impact factor:   4.285


  15 in total

1.  Phenotype screening for genetically determined age-onset disorders and increased longevity in ENU-mutagenized mice.

Authors:  Dabney K Johnson; Eugene M Rinchik; Naima Moustaid-Moussa; Darla R Miller; Robert W Williams; Edward J Michaud; Monica M Jablonski; Andrea Elberger; Kristen Hamre; Richard Smeyne; Elissa Chesler; Daniel Goldowitz
Journal:  Age (Dordr)       Date:  2005-05-02

2.  The improvement in fertilizing ability of cryopreserved mouse spermatozoa using laser-microdissected oocytes.

Authors:  Takehito Kaneko; Miho Yanagi; Tatsuyuki Nakashima; Naomi Nakagata
Journal:  Reprod Med Biol       Date:  2006-11-23

3.  Oocytes from female mice on MF1 genetic background are not suitable for assisted reproduction†.

Authors:  Yasushiro Yamauchi; Anna Ajduk; Monika A Ward
Journal:  Biol Reprod       Date:  2020-03-13       Impact factor: 4.285

4.  Mitochondrial hydrogen peroxide and defective cholesterol efflux prevent in vitro fertilization by cryopreserved inbred mouse sperm.

Authors:  Jeffrey E Gray; Joshua Starmer; Vivian S Lin; Bryan C Dickinson; Terry Magnuson
Journal:  Biol Reprod       Date:  2013-07-25       Impact factor: 4.285

5.  Spermatozoa and spermatids retrieved from frozen reproductive organs or frozen whole bodies of male mice can produce normal offspring.

Authors:  Narumi Ogonuki; Keiji Mochida; Hiromi Miki; Kimiko Inoue; Martin Fray; Takamasa Iwaki; Kazuo Moriwaki; Yuichi Obata; Kazuto Morozumi; Ryuzo Yanagimachi; Atsuo Ogura
Journal:  Proc Natl Acad Sci U S A       Date:  2006-08-18       Impact factor: 11.205

6.  Archiving and distributing mouse lines by sperm cryopreservation, IVF, and embryo transfer.

Authors:  Hideko Takahashi; Chengyu Liu
Journal:  Methods Enzymol       Date:  2010       Impact factor: 1.600

7.  The effect on intracytoplasmic sperm injection outcome of genotype, male germ cell stage and freeze-thawing in mice.

Authors:  Narumi Ogonuki; Manami Mori; Akie Shinmen; Kimiko Inoue; Keiji Mochida; Akihiko Ohta; Atsuo Ogura
Journal:  PLoS One       Date:  2010-06-11       Impact factor: 3.240

8.  Assisted reproduction technologies impair placental steroid metabolism.

Authors:  Abby C Collier; Shogo J Miyagi; Yasuhiro Yamauchi; Monika A Ward
Journal:  J Steroid Biochem Mol Biol       Date:  2009-05-03       Impact factor: 4.292

9.  Effect of IVF and laser zona dissection on DNA methylation pattern of mouse zygotes.

Authors:  Dominika D Peters; Konstantin Lepikhov; Karsten Rodenacker; Susan Marschall; Auke Boersma; Peter Hutzler; Hagen Scherb; Jörn Walter; Martin Hrabé de Angelis
Journal:  Mamm Genome       Date:  2009-10-13       Impact factor: 2.957

10.  Biopsy of embryos produced by in vitro fertilization affects development in C57BL/6 mouse strain.

Authors:  Atsushi Sugawara; Monika A Ward
Journal:  Theriogenology       Date:  2012-11-19       Impact factor: 2.740

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