Author/Authors :
Miraki, Saber Department of Anatomy - Faculty of Medicine - Kurdistan University of Medical Sciences, Sanandaj, Iran , Mokarizadeh, Aram Department of Immunology and Hematology - Faculty of Medicine - Kurdistan University of Medical Sciences, Sanandaj, Iran , Banafshi, Omid Cellular and Molecular Research Center - Faculty of Medicine - Kurdistan University of Medical Sciences, Sanandaj, Iran , Assadollahi, Vahideh Cellular and Molecular Research Center - Faculty of Medicine - Kurdistan University of Medical Sciences, Sanandaj, Iran , Abdi, Mahdad Department of Anatomy - Faculty of Medicine - Kurdistan University of Medical Sciences, Sanandaj, Iran , Roshani, Daem Social Determinants of Health Research Center - Kurdistan University of Medical Sciences, Sanandaj, Iran , Fathi, Fardin Cellular and Molecular Research Center - Faculty of Medicine - Kurdistan University of Medical Sciences, Sanandaj, Iran
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.
Keywords :
Mice , Embryonic stem cells , Assisted reproductive technologies , Oocytes