Literature DB >> 19864014

Production of good-quality porcine blastocysts by in vitro fertilization of follicular oocytes vitrified at the germinal vesicle stage.

T Somfai1, J Noguchi, H Kaneko, M Nakai, M Ozawa, N Kashiwazaki, I Egerszegi, J Rátky, T Nagai, K Kikuchi.   

Abstract

We investigated survival, meiotic competence, cytoplasmic maturation, in vitro fertilization, and development of immature porcine (Sus scrofa) oocytes cryopreserved by a modified solid surface vitrification protocol. Cumulus-oocyte complexes (COCs) collected from follicles 3 to 6mm in diameter in abattoir-derived ovaries of prepubertal gilts were either vitrified (Vitrified group), subjected to cryoprotectant treatment (CPA group), or used without any treatment (Control group). Oocyte viability was assayed by staining with fluorescein diacetate. Live oocytes were matured in vitro and their meiotic progression investigated by nuclear staining. In a series of experiments, the glutathione (GSH) content of in vitro-matured oocytes and viability of cumulus cells were assayed simultaneously. The in vitro-matured oocytes were also fertilized and cultured in vitro to assess their ability to be fertilized and to develop to the blastocyst stage, respectively. The proportion of viable oocytes in the Vitrified group was significantly lower than that in the CPA and Control groups (27.7%, 90.4%, and 100%, respectively). Among the three groups, there were no differences in meiotic competence, cumulus viability, and GSH levels at the end of in vitro maturation. Fertilization parameters (i.e., rates of male pronucleus formation, monospermy, and second polar body extrusion) were also similar among groups. However, comparison of the developmental abilities of oocytes in the Vitrified, CPA, and Control groups revealed that the Vitrified group had a significantly reduced ability to undergo first cleavage (34.4%, 63.3%, and 69.0%) and to develop to the blastocyst stage (5.1%, 25.5%, and 34.6%). The mean total cell numbers in blastocysts after 6 d of culture were not significantly different among the Vitrified, CPA, and Control groups (40.3, 42.8, and 43.4). In conclusion, despite low survival rates and impaired development in the Vitrified group, meiotic competence, cytoplasmic maturation, and subsequent fertilization characteristics of surviving germinal vesicle oocytes were unaffected by vitrification, and high-quality blastocysts were produced from vitrified immature oocytes.

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Year:  2010        PMID: 19864014     DOI: 10.1016/j.theriogenology.2009.08.008

Source DB:  PubMed          Journal:  Theriogenology        ISSN: 0093-691X            Impact factor:   2.740


  7 in total

1.  Vitrification of pig oocytes induces changes in histone H4 acetylation and histone H3 lysine 9 methylation (H3K9).

Authors:  M Spinaci; C Vallorani; D Bucci; C Tamanini; E Porcu; G Galeati
Journal:  Vet Res Commun       Date:  2012-06-17       Impact factor: 2.459

2.  An efficiency comparison of different in vitro fertilization methods: IVF, ICSI, and PICSI for embryo development to the blastocyst stage from vitrified porcine immature oocytes.

Authors:  Fahiel Casillas; Miguel Betancourt; Cristina Cuello; Yvonne Ducolomb; Alma López; Lizbeth Juárez-Rojas; Socorro Retana-Márquez
Journal:  Porcine Health Manag       Date:  2018-08-13

3.  Embryo production by intracytoplasmic injection of sperm retrieved from Meishan neonatal testicular tissue cryopreserved and grafted into nude mice.

Authors:  Hiroyuki Kaneko; Kazuhiro Kikuchi; Nguyen Thi Men; Junko Noguchi
Journal:  Anim Sci J       Date:  2018-12-06       Impact factor: 1.749

4.  Vitrification of porcine cumulus-oocyte complexes at the germinal vesicle stage does not trigger apoptosis in oocytes and early embryos, but activates anti-apoptotic Bcl-XL gene expression beyond the 4-cell stage.

Authors:  Tamás Somfai; Hiep Thi Nguyen; Men Thi Nguyen; Thanh Quang Dang-Nguyen; Hiroyuki Kaneko; Junko Noguchi; Kazuhiro Kikuchi
Journal:  J Reprod Dev       Date:  2020-01-27       Impact factor: 2.214

5.  Generation of live piglets for the first time using sperm retrieved from immature testicular tissue cryopreserved and grafted into nude mice.

Authors:  Hiroyuki Kaneko; Kazuhiro Kikuchi; Michiko Nakai; Tamas Somfai; Junko Noguchi; Fuminori Tanihara; Junya Ito; Naomi Kashiwazaki
Journal:  PLoS One       Date:  2013-07-29       Impact factor: 3.240

6.  Comparison of ethylene glycol and propylene glycol for the vitrification of immature porcine oocytes.

Authors:  Tamás Somfai; Michiko Nakai; Fuminori Tanihara; Junko Noguchi; Hiroyuki Kaneko; Naomi Kashiwazaki; István Egerszegi; Takashi Nagai; Kazuhiro Kikuchi
Journal:  J Reprod Dev       Date:  2013-05-10       Impact factor: 2.214

7.  Optimization of cryoprotectant treatment for the vitrification of immature cumulus-enclosed porcine oocytes: comparison of sugars, combinations of permeating cryoprotectants and equilibration regimens.

Authors:  Tamás Somfai; Nguyen Thi Men; Junko Noguchi; Hiroyuki Kaneko; Naomi Kashiwazaki; Kazuhiro Kikuchi
Journal:  J Reprod Dev       Date:  2015-09-27       Impact factor: 2.214

  7 in total

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