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Embryonic Stem Cell Conditioned Medium Supports In Vitro Maturation of Mouse Oocytes.
Miraki, Saber; Mokarizadeh, Aram; Banafshi, Omid; Assadollahi, Vahideh; Abdi, Mahdad; Roshani, Daem; Fathi, Fardin.
Affiliation
  • Miraki S; Department of Anatomy, Faculty of Medicine, Kurdistan University of Medical Sciences, Sanandaj, Iran.
  • Mokarizadeh A; Department of Immunology and Hematology, Faculty of Medicine, Kurdistan University of Medical Sciences, Sanandaj, Iran.
  • Banafshi O; Cellular and Molecular Research Center, Faculty of Medicine, Kurdistan University of Medical Sciences, Sanandaj, Iran.
  • Assadollahi V; Cellular and Molecular Research Center, Faculty of Medicine, Kurdistan University of Medical Sciences, Sanandaj, Iran.
  • Abdi M; Department of Anatomy, Faculty of Medicine, Kurdistan University of Medical Sciences, Sanandaj, Iran.
  • Roshani D; Social Determinants of Health Research Center, Kurdistan University of Medical Sciences, Sanandaj, Iran.
  • Fathi F; Cellular and Molecular Research Center, Faculty of Medicine, Kurdistan University of Medical Sciences, Sanandaj, Iran.
Avicenna J Med Biotechnol ; 9(3): 114-119, 2017.
Article de En | MEDLINE | ID: mdl-28706605
ABSTRACT

BACKGROUND:

This study aimed to investigate the maturation and fertilization rates of immature mouse oocytes using Embryonic Stem Cell Conditioned Medium (ESCM).

METHODS:

Germinal Vesicle (GV) stage oocytes were observed in 120 NMRI mice, aged 4-6 weeks. GV oocytes with or without cumulus cells were subjected to IVM in either ESCM, Embryonic Stem Cell Growth Medium (ESGM), or α-minimum essential medium (α-MEM). After recording the Metaphase II (MII) oocyte maturation rate, the oocytes were fertilized in vitro. The fertilization success rate was recorded after 24 hr. The embryos were maintained in potassium Simplex Optimization Medium (KSOM) for 96 hr and allowed to grow until the blastocyst stage. After recording developmental competence, they were transferred into the uteri of pseudopregnant mice and their birth rates were recorded.

RESULTS:

No significant difference existed between the maturation rates in α-MEM (68.18%) and ESCM (64.67%; p>0.05), whereas this rate was significantly higher for both α-MEM and ESCM compared to ESGM (32.22%; p<0.05). A significant difference in IVF success rate existed for oocytes grown in α-MEM (69.44%), ESCM (61.53%), and ESGM (0%). A significantly higher developmental competence was observed at the blastocyst stage for oocytes grown in α-MEM (51.2%) compared to ESCM (35%; p<0.05). 17 days after embryo transfer into the uteri of pseudopregnant mice, there was a nonsignficant (p>0.05), similar birth rate between α-MEM and ESCM (47 vs. 40%).

CONCLUSION:

ESCM is an effective medium for preantral follicle growth, oocyte maturation, and subsequent embryo development.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Avicenna J Med Biotechnol Année: 2017 Type de document: Article Pays d'affiliation: Iran

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Avicenna J Med Biotechnol Année: 2017 Type de document: Article Pays d'affiliation: Iran