Literature DB >> 16128410

Medium effects on capacitation and sperm penetration through the zona pellucida in inbred BALB/c spermatozoa.

Seiji Kito1, Yuki Ohta.   

Abstract

Inbred BALB/c mice are one of the most difficult inbred strains to fertilize in vitro. In this study we examined the abilities of various media used for mouse in vitro fertilization (IVF) to support capacitation and sperm penetration through the zona pellucida (ZP) of inbred BALB/c spermatozoa. Media examined were TYH, M16, CZB, mWhitten medium, T6, modified Tyrode's solution (mTyrode's), mKSOM, MEM and TCM199. Modified human tubal fluid (mHTF) was used as a control medium. When sperm were capacitated and inseminated in the same medium, mHTF showed the best fertilization (approximately 80%) scored by male pronuclear formation (<26%) at 5h post-insemination (PI). When sperm were capacitated in various media and inseminated in mHTF, sperm capacitated in TYH solution (93%) but no other media (<45%) showed a significantly higher level of sperm nuclear decondensation (SND) than mHTF at 2 h PI (approximately 65%). When sperm were capacitated in mHTF and inseminated in various media, only mTyrode's (52%) was not significantly lower than mHTF (66%) in terms of SND at 2h PI (<49%). Sperm capacitation also was examined by chlortetracycline (CTC) staining. Sperm capacitated in TYH solution showed a significantly higher percentage of capacitation (46%) than those treated in HTF (28%) and other media (<24%). These results indicate that the best approach for IVF in the BALB/c strain is capacitation in TYH and insemination in mHTF. Poor fertilization of BALB/c may result from suboptimal conditions of sperm capacitation and insemination, and overall IVF success may differ depending on strains used.

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Year:  2005        PMID: 16128410     DOI: 10.1017/s0967199405003205

Source DB:  PubMed          Journal:  Zygote        ISSN: 0967-1994            Impact factor:   1.442


  5 in total

1.  A protocol for rat in vitro fertilization during conventional laboratory working hours.

Authors:  Toshihiro Aoto; Ri-ichi Takahashi; Masatsugu Ueda
Journal:  Transgenic Res       Date:  2011-02-26       Impact factor: 2.788

Review 2.  Overview of new developments in and the future of cryopreservation in the laboratory mouse.

Authors:  Mo Guan; Susan Marschall; Marcello Raspa; Amanda R Pickard; Martin D Fray
Journal:  Mamm Genome       Date:  2012-08-31       Impact factor: 2.957

3.  Epigenetic effect of putrescine supplementation during in vitro maturation of oocytes on offspring in mice.

Authors:  Chennan Shi; Jingyi Zhang; Zhengjie Yan; Li Gao; Chao Gao; Wei Wu; Jiayin Liu; Yugui Cui
Journal:  J Assist Reprod Genet       Date:  2022-03-07       Impact factor: 3.412

4.  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

5.  Conserving, distributing and managing genetically modified mouse lines by sperm cryopreservation.

Authors:  G Charles Ostermeier; Michael V Wiles; Jane S Farley; Robert A Taft
Journal:  PLoS One       Date:  2008-07-30       Impact factor: 3.240

  5 in total

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