玻璃化
胚泡
男科
低温保护剂
胚胎
低温保存
人类受精
卵母细胞
体外成熟
胚胎发生
生物
化学
解剖
医学
细胞生物学
作者
Lianyu Shi,Hai-feng Jin,Jung-Gon Kim,B. Mohana Kumar,S. Balasubramanian,S.Y. Choe,Gyu‐Jin Rho
标识
DOI:10.1016/j.anireprosci.2006.06.020
摘要
This study evaluated the effects of exposure and/or vitrification of porcine metaphase II (MII) oocytes on their in vitro viability and ultra-structural changes with two experiments. Experiment 1 examined the effect of vitrified oocytes on microtubule localization, mitochondrial morphology, chromosome organization and the developmental rate in IVF control and vitrified oocytes. Oocytes matured for 44 h were subjected to IVF (IVF control). Oocytes matured for 42 h were exposed to cryoprotectants (CPA control), followed by 2 h culture, and subjected to IVF. Oocytes vitrified at 42 h post-maturation were warmed, cultured for 2 h, and subjected to IVF (vitrified). Experiment 2 evaluated the effect of oocytes freezing on development of ICSI with and without activation and parthenotes. Fresh and vitrified oocytes were subjected to ICSI with and without electrical activation. Cleavage and blastocyst rates were significantly (P < 0.05) lower in vitrified IVF, parthenote and ICSI embryos than those in fresh counterparts. Between ICSI embryos from fresh oocytes and vitrified oocytes, the rates of blastocyst were significantly higher (P < 0.05) in activated group than the group without activation. Significant differences (P < 0.05) were observed in normal spindle configuration of vitrified (43.5%) compared to control (81.0%) oocytes, but no significant difference was observed between CPA exposed and control groups. In conclusion, porcine oocytes at MII stage are very sensitive to vitrification with altered microtubule localization and mitochondrial organization thus resulting in impaired fertilization and embryo development.
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