Literature DB >> 9369169

Positive effect of partial zona-pellucida dissection on the in vitro fertilizing capacity of cryopreserved C57BL/6J transgenic mouse spermatozoa of low motility.

N Nakagata1, M Okamoto, O Ueda, H Suzuki.   

Abstract

Although cryopreservation of mouse spermatozoa has recently become available for use, as yet there are considerable differences in fertilization efficiency of cryopreserved spermatozoa among various mouse strains. In this study, oocytes subjected to partial dissection of the zona pellucida (PZD) were inseminated with frozen-thawed C57BL/6J mouse spermatozoa. At 30, 60, 120, and 240 min after insemination, the oocytes were washed in human tubal fluid medium and cultured for 3-6 h. The fertilization rates of the PZD oocytes in each group at 6-7 h after insemination were significantly higher than that of the zona-intact control (73-88% vs 12%, respectively) (p < 0.01); but the incidence of polyspermy was nevertheless quite low (1.3-2.4%). The development rates of the monospermic oocytes to the morula and early blastocyst stages were in the 87-92% range, with 31-40% of those developing into offspring after embryo transfer. When the cryopreserved spermatozoa of C57BL/6J transgenic mice were used to fertilize PZD oocytes, the fertilization rates were as high as (73-76%) those of the PZD oocytes inseminated with the cryopreserved C57BL/6J spermatozoa, with 30-31% of the morulae and early blastocysts derived from the monospermatic oocytes developing into offspring. These results indicate that PZD of oocytes may provide an alternative when the fertilizing capacity of mouse spermatozoa has been compromised by cryopreservation.

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Year:  1997        PMID: 9369169     DOI: 10.1095/biolreprod57.5.1050

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


  20 in total

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2.  Optimization of cryoprotectant loading into murine and human oocytes.

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Review 4.  Simple gamete preservation and artificial reproduction of mammals using micro-insemination techniques.

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Review 5.  Overview of new developments in and the future of cryopreservation in the laboratory mouse.

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Journal:  Mamm Genome       Date:  2012-08-31       Impact factor: 2.957

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

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Journal:  Biol Reprod       Date:  2013-07-25       Impact factor: 4.285

8.  Combinational Treatment of Trichostatin A and Vitamin C Improves the Efficiency of Cloning Mice by Somatic Cell Nuclear Transfer.

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9.  Inhibition of in vitro fertilizing capacity of cryopreserved mouse sperm by factors released by damaged sperm, and stimulation by glutathione.

Authors:  Mary L Bath
Journal:  PLoS One       Date:  2010-02-24       Impact factor: 3.240

10.  Safety, efficacy and efficiency of laser-assisted IVF in subfertile mutant mouse strains.

Authors:  Ming-Wen Li; Kristy L Kinchen; Jadine M Vallelunga; Diana L Young; Kaleb D K Wright; Lisa N Gorano; Katherine Wasson; K C Kent Lloyd
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