Literature DB >> 23846105

Applications of cryopreserved unfertilized mouse oocytes for in vitro fertilization.

Naomi Nakagata1, Toru Takeo, Kiyoko Fukumoto, Tomoko Kondo, Yukie Haruguchi, Yumi Takeshita, Yuko Nakamuta, Hiroko Matsunaga, Shuuji Tsuchiyama, Yuta Ishizuka, Kimi Araki.   

Abstract

Since the first successful reports into oocyte freezing, many papers concerning the cryopreservation of mouse oocytes have been published. However, a simple and practical cryopreservation method for unfertilized C57BL/6 mouse oocytes, and an IVF system using these cryopreserved oocytes have yet to be established, in spite of the fact that C57BL/6 is the prevalent inbred strain and is used for large-scale knockout programs. In this study, unfertilized C57BL/6 mouse oocytes were cryopreserved via a simple vitrification method. After warming, IVF was performed using cryopreserved unfertilized oocytes and fresh sperm, cryopreserved unfertilized oocytes and cold-stored sperm, cryopreserved unfertilized oocytes and frozen sperm (C57BL/6 strain sperm), and cryopreserved unfertilized oocytes and frozen sperm derived from GEM strains (C57BL/6 background GEM strains). Nearly all of the cryopreserved oocytes were recovered, of which over 90% were morphologically normal. Those oocytes were then used for in vitro fertilization, resulting in 72-97% of oocytes developing into 2-cell embryos. A portion of the 2-cell embryos were transferred to recipients, resulting in live young being produced from 32-49% of the embryos. In summary, we established the simple and practical method of mouse oocyte vitrification with high survivability and developmental ability and the IVF using the vitrified-warmed oocytes with fresh, cold-stored or cryopreserved sperm with high fertility.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cold-stored sperm; Cryopreserved sperm; Fresh Sperm; In vitro fertilization; Mouse; Oocyte vitrification

Mesh:

Year:  2013        PMID: 23846105     DOI: 10.1016/j.cryobiol.2013.06.011

Source DB:  PubMed          Journal:  Cryobiology        ISSN: 0011-2240            Impact factor:   2.487


  16 in total

1.  Investigations of motility and fertilization potential in thawed cryopreserved mouse sperm from cold-stored epididymides.

Authors:  Toru Takeo; Kiyoko Fukumoto; Tomoko Kondo; Yukie Haruguchi; Yumi Takeshita; Yuko Nakamuta; Shuuji Tsuchiyama; Hidetaka Yoshimoto; Norihiko Shimizu; Ming-Wen Li; Kristy Kinchen; Jadine Vallelunga; K C Kent Lloyd; Naomi Nakagata
Journal:  Cryobiology       Date:  2013-11-04       Impact factor: 2.487

2.  Impact of prolonged oocyte incubation time before vitrification on oocyte survival, embryo formation, and embryo quality in mice.

Authors:  Azade Karami; Mitra Bakhtiari; Mehri Azadbakht; Rostam Ghorbani; Mozafar Khazaei; Mansour Rezaei
Journal:  In Vitro Cell Dev Biol Anim       Date:  2017-02-03       Impact factor: 2.416

3.  Superovulation using the combined administration of inhibin antiserum and equine chorionic gonadotropin increases the number of ovulated oocytes in C57BL/6 female mice.

Authors:  Toru Takeo; Naomi Nakagata
Journal:  PLoS One       Date:  2015-05-29       Impact factor: 3.240

4.  Production of knockout mice by DNA microinjection of various CRISPR/Cas9 vectors into freeze-thawed fertilized oocytes.

Authors:  Yoshiko Nakagawa; Tetsushi Sakuma; Takuya Sakamoto; Masaki Ohmuraya; Naomi Nakagata; Takashi Yamamoto
Journal:  BMC Biotechnol       Date:  2015-05-22       Impact factor: 2.563

5.  Laser-assisted in vitro fertilization facilitates fertilization of vitrified-warmed C57BL/6 mouse oocytes with fresh and frozen-thawed spermatozoa, producing live pups.

Authors:  Stephanie E Woods; Peimin Qi; Elizabeth Rosalia; Tony Chavarria; Allan Discua; John Mkandawire; James G Fox; Alexis García
Journal:  PLoS One       Date:  2014-03-11       Impact factor: 3.240

6.  Culture time of vitrified/warmed zygotes before microinjection affects the production efficiency of CRISPR-Cas9-mediated knock-in mice.

Authors:  Yoshiko Nakagawa; Tetsushi Sakuma; Norihisa Nishimichi; Yasuyuki Yokosaki; Toru Takeo; Naomi Nakagata; Takashi Yamamoto
Journal:  Biol Open       Date:  2017-05-15       Impact factor: 2.422

7.  Rescue in vitro fertilization method for legacy stock of frozen mouse sperm.

Authors:  Naomi Nakagata; Toru Takeo; Kiyoko Fukumoto; Yukie Haruguchi; Tomoko Kondo; Yumi Takeshita; Yuko Nakamuta; Tomoko Umeno; Shuuji Tsuchiyama
Journal:  J Reprod Dev       Date:  2014-02-04       Impact factor: 2.214

8.  Application of oocyte cryopreservation technology in TALEN-mediated mouse genome editing.

Authors:  Yoshiko Nakagawa; Tetsushi Sakuma; Naomi Nakagata; Sho Yamasaki; Naoki Takeda; Masaki Ohmuraya; Takashi Yamamoto
Journal:  Exp Anim       Date:  2014

9.  Prolonged exposure to hyaluronidase decreases the fertilization and development rates of fresh and cryopreserved mouse oocytes.

Authors:  Yuta Ishizuka; Toru Takeo; Satohiro Nakao; Hidetaka Yoshimoto; Yumiko Hirose; Yuki Sakai; Yuka Horikoshi; Shiori Takeuji; Shuuji Tsuchiyama; Naomi Nakagata
Journal:  J Reprod Dev       Date:  2014-09-12       Impact factor: 2.214

10.  Ultra-superovulation for the CRISPR-Cas9-mediated production of gene-knockout, single-amino-acid-substituted, and floxed mice.

Authors:  Yoshiko Nakagawa; Tetsushi Sakuma; Norihisa Nishimichi; Yasuyuki Yokosaki; Noriyuki Yanaka; Toru Takeo; Naomi Nakagata; Takashi Yamamoto
Journal:  Biol Open       Date:  2016-08-15       Impact factor: 2.422

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