Literature DB >> 18408352

Defined system for in vitro production of porcine embryos using a single basic medium.

Koji Yoshioka1, Chie Suzuki, Akira Onishi.   

Abstract

We have previously indicated that porcine blastocysts can be produced by in vitro fertilization (IVF) and culture (IVC) in chemically defined porcine gamete medium (PGM) and porcine zygote medium (PZM)-5, respectively, In the present study, the effects of basic media and macromolecular components on in vitro maturation (IVM) were investigated to develop a defined system for in vitro embryo production using a single basic medium through IVM, IVF and IVC. Porcine immature oocytes were matured in porcine oocyte medium (POM) or modified North Carolina State University (mNCSU) 37, which were supplemented with either 10% (v/v) porcine follicular fluid (pFF) or 3 mg/ml polyvinyl alcohol (PVA) as a macromolecular component (designated POM+pFF, POM+PVA, mNCSU37+pFF and mNCSU37+PVA). In the maturation with mNCSU37+PVA, the percentages of oocytes that reached the metaphase II stages were significantly lower than those in the other treatments. Following IVM with the above media, oocytes were treated with an electrical stimulus and cycloheximide for parthenogenetic activation and were cultured in PZM-5 for 5 days. The rates of cleavage and blastocyst formation of parthenogenetic oocytes were significantly lowered for maturation with mNCSU37+PVA compared with the other treatments, while there were no significant differences in the total numbers of cells in blastocysts among the treatments. Following IVF and IVC, the rates of penetration, male pronucleus formation, cleavage and blastocyst formation were significantly lower when oocytes were matured in mNCSU37+PVA than in other maturation media. The normal fertilization rate was significantly higher in POM+PVA compared with the other treatments, although the total number of cells in blastocysts was reduced with the addition of PVA to both POM and mNCSU37 compared with pFF supplementation. These results demonstrate that porcine blastocysts can be produced by the defined system using a single basic medium.

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Year:  2008        PMID: 18408352     DOI: 10.1262/jrd.20001

Source DB:  PubMed          Journal:  J Reprod Dev        ISSN: 0916-8818            Impact factor:   2.214


  33 in total

1.  Modifications of human growth differentiation factor 9 to improve the generation of embryos from low competence oocytes.

Authors:  Jing-Jie Li; Satoshi Sugimura; Thomas D Mueller; Melissa A White; Georgia A Martin; Lesley J Ritter; Xiao-Yan Liang; Robert B Gilchrist; David G Mottershead
Journal:  Mol Endocrinol       Date:  2015-01

2.  Follicular factors determining granulosa cell number and developmental competence of porcine oocytes.

Authors:  Yasuhisa Munakata; Manami Ueda; Ryoka Kawahara-Miki; Kazuki Kansaku; Nobuhiko Itami; Koumei Shirasuna; Takehito Kuwayama; Hisataka Iwata
Journal:  J Assist Reprod Genet       Date:  2018-07-12       Impact factor: 3.412

3.  Small-extracellular vesicles and their microRNA cargo from porcine follicular fluids: the potential association with oocyte quality.

Authors:  Ahmed Gad; Matej Murin; Alexandra Bartkova; Veronika Kinterova; Katerina Marcollova; Jozef Laurincik; Radek Prochazka
Journal:  J Anim Sci Biotechnol       Date:  2022-06-20

4.  Effects of In Vitro Maturation on Histone Acetylation in Metaphase II Oocytes and Early Cleavage Embryos.

Authors:  Ning Wang; Fang Le; Qi-Tao Zhan; Li Li; Min-Yue Dong; Guo-Lian Ding; Chen-Ming Xu; Shi-Wen Jiang; He-Feng Huang; Fan Jin
Journal:  Obstet Gynecol Int       Date:  2010-06-20

5.  Cumulin, an Oocyte-secreted Heterodimer of the Transforming Growth Factor-β Family, Is a Potent Activator of Granulosa Cells and Improves Oocyte Quality.

Authors:  David G Mottershead; Satoshi Sugimura; Sara L Al-Musawi; Jing-Jie Li; Dulama Richani; Melissa A White; Georgia A Martin; Andrew P Trotta; Lesley J Ritter; Junyan Shi; Thomas D Mueller; Craig A Harrison; Robert B Gilchrist
Journal:  J Biol Chem       Date:  2015-08-08       Impact factor: 5.157

6.  Generating porcine chimeras using inner cell mass cells and parthenogenetic preimplantation embryos.

Authors:  Kazuaki Nakano; Masahito Watanabe; Hitomi Matsunari; Taisuke Matsuda; Kasumi Honda; Miki Maehara; Takahiro Kanai; Gota Hayashida; Mirina Kobayashi; Momoko Kuramoto; Yoshikazu Arai; Kazuhiro Umeyama; Shuh-Hei Fujishiro; Yoshihisa Mizukami; Masaki Nagaya; Yutaka Hanazono; Hiroshi Nagashima
Journal:  PLoS One       Date:  2013-04-23       Impact factor: 3.240

7.  Mural granulosa cells support to maintain the viability of growing porcine oocytes and its developmental competence after insemination.

Authors:  Takayuki Yamochi; Shu Hashimoto; Yoshiharu Morimoto
Journal:  J Assist Reprod Genet       Date:  2021-05-10       Impact factor: 3.357

8.  Trehalose in glycerol-free freezing extender enhances post-thaw survival of boar spermatozoa.

Authors:  Rukmali Athurupana; Daisen Takahashi; Sumire Ioki; Hiroaki Funahashi
Journal:  J Reprod Dev       Date:  2015-03-07       Impact factor: 2.214

9.  Successful production of piglets derived from expanded blastocysts vitrified using a micro volume air cooling method without direct exposure to liquid nitrogen.

Authors:  Koji Misumi; Yuri Hirayama; Sachiko Egawa; Shoko Yamashita; Hiroyoshi Hoshi; Kei Imai
Journal:  J Reprod Dev       Date:  2013-08-15       Impact factor: 2.214

10.  In vitro fertilization and development of porcine oocytes matured in follicular fluid.

Authors:  Budiyanto Agung; Takeshige Otoi; Dai-ichiro Fuchimoto; Shoichiro Senbon; Akira Onishi; Takashi Nagai
Journal:  J Reprod Dev       Date:  2013-02-20       Impact factor: 2.214

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