Developmental competence of human embryos derived from in vitro maturation of immature oocytes retrieved during cesarean section

2013 ◽  
Vol 40 (2) ◽  
pp. 459-464 ◽  
Author(s):  
Pallop Pongsuthirak ◽  
Teraporn Vutyavanich
Keyword(s):  
Cesarean Section ◽  
In Vitro Maturation ◽  
Developmental Competence ◽  
Human Embryos ◽  
Immature Oocytes

209 MATURATION KINETICS AFTER HOLDING EQUINE OOCYTES IN EMBRYO HOLDING MEDIUM

2016 ◽  
Vol 28 (2) ◽  
pp. 235
Author(s):  
P. Dini ◽  
O. Bogado ◽  
K. Smits ◽  
A. VanSoom ◽  
P. Daels
Keyword(s):  
In Vitro Maturation ◽  
Polar Body ◽  
Developmental Competence ◽  
Hoechst 33342 ◽  
Immature Oocytes ◽  
Maturation Rate ◽  
Chromatin Configuration ◽  
One Way Anova ◽  
Selection Of

It has been reported that immature, equine oocytes can be maintained in meiotic arrest at 24°C. To evaluate a commercial equine embryo holding medium for storage of equine oocyte at 24°C and to determine the effect of holding on maturation kinetics, cumulus‐oocyte complexes (COC) were recovered from slaughtered mares and placed in Syngro® Embryo Holding Solution at 22–25°C for 18–20 h (OH Group) or placed directly in DMEM-F12-based in vitro maturation (IVM) conditions (D-Mat Group) at 5% CO2 in air at 38.5°C. Maturation rate (metaphase II percentage; MII%) was assessed (presence of polar body under stereomicroscope) after denudation at 22, 24, and 28 h. After assessment, the denuded oocytes that were considered immature were placed back in IVM, reassessed at 24 and 28 h, and MII% was compared with that of oocytes remaining uninterrupted in IVM for 24 and 28 h. One-way ANOVA was used to compare dependent variable in different groups using PROC ANOVA (SAS, version 9.2, SAS Institute, Cary, NC, USA). A random selection of mature oocytes from both groups were fertilised using intracytoplasmic sperm injection (ICSI). A total of 250 injected oocytes were cultured in DMEM-F12 with 10% FCS. Blastocyst rates in OH and D-mat groups were similar (7.1% v. 6.3%). At 22 h, significantly more oocytes reached the MII stage in the OH group than in the D-Mat group, but MII% was similar in both groups at 24 and 28 h (Table 1). Denuded, immature oocytes reached similar maturation rate as the undenuded oocytes in the same group. Our data suggest that oocytes can be held in Syngro® Embryo Holding Solution at 22–25°C for 18–20 h without compromising oocyte developmental competence. Overnight holding of oocytes accelerates maturation with similar maturation rate at 22, 24, and 28 h of IVM in the OH group. Denudation of immature oocytes after 22 h of IVM and returning the denuded oocytes to IVM does not affect the progression of maturation. In subsequent experiment, overnight held oocytes were fixed and stained (Hoechst 33342) and MII% was evaluated after 20, 22, and 28 h of IVM. Chromatin configuration confirmed that stored oocytes reach the MII stage at 22 h. Maturation rates were significantly lower at 20 h, suggesting that 22 h of IVM is required for stored oocytes. Table 1.Maturation rates (% in MII stage) at 22, 24, and 28 h of IVM for equine oocytes held in Syngro® Embryo Holding Medium before IVM (OH) and oocytes placed directly in IVM (D-Mat) Thanks to I. Lemahieu and P. Van Damme. Study was supported by the Special Research Fund at UGent.

scholarly journals Cortical Granule Distribution and Expression Pattern of Genes Regulating Cellular Component Size, Morphogenesis, and Potential to Differentiation are Related to Oocyte Developmental Competence and Maturational Capacity In Vivo and In Vitro

Genes ◽  
2020 ◽  
Vol 11 (7) ◽  
pp. 815
Author(s):  
Magdalena Kulus ◽  
Wiesława Kranc ◽  
Michal Jeseta ◽  
Patrycja Sujka-Kordowska ◽  
Aneta Konwerska ◽  
...  
Keyword(s):  
In Vitro Maturation ◽  
Developmental Competence ◽  
Egg Cell ◽  
Cortical Granule ◽  
Distribution Analysis ◽  
Cortical Granules ◽  
Immature Oocytes ◽  
Component Size ◽  
Meiotic Competence

Polyspermia is an adverse phenomenon during mammalian fertilization when more than one sperm fuses with a single oocyte. The egg cell is prepared to prevent polyspermia by, among other ways, producing cortical granules (CGs), which are specialized intracellular structures containing enzymes that aim to harden the zona pellucida and block the fusion of subsequent sperm. This work focused on exploring the expression profile of genes that may be associated with cortical reactions, and evaluated the distribution of CGs in immature oocytes and the peripheral density of CGs in mature oocytes. Oocytes were isolated and then processed for in vitro maturation (IVM). Transcriptomic analysis of genes belonging to five ontological groups has been conducted. Six genes showed increased expression after IVM (ARHGEF2, MAP1B, CXCL12, FN1, DAB2, and SOX9), while the majority of genes decreased expression after IVM. Using CG distribution analysis in immature oocytes, movement towards the cortical zone of the oocyte during meiotic competence acquisition was observed. CGs peripheral density decreased with the rise in meiotic competence during the IVM process. The current results reveal important new insights into the in vitro maturation of oocytes. Our results may serve as a basis for further studies to investigate the cortical reaction of oocytes.

scholarly journals The Novel Pig In Vitro Maturation System to Improve Developmental Competence of Oocytes Derived from Atretic Nonvascularized Follicles

2016 ◽  
Vol 95 (4) ◽  
pp. 76-76 ◽  
Author(s):  
A. Okamoto ◽  
M. Ikeda ◽  
A. Kaneko ◽  
C. Kishida ◽  
M. Shimada ◽  
...  
Keyword(s):  
In Vitro Maturation ◽  
Developmental Competence ◽  
The Novel
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