玻璃化
胚泡
脂肪酸
男科
胚胎
生物
低温保存
生物化学
化学
细胞生物学
胚胎发生
医学
作者
Kazuki Ohata,Kenji Ezoe,Tetsuya Miki,Shizu Kouraba,Nanoha Fujiwara,Akiko Yabuuchi,Tamotsu Kobayashi,Keiichi Kato
标识
DOI:10.1016/j.rbmo.2021.03.022
摘要
Abstract Research question Does fatty acid supplementation in vitrification and warming media influence developmental competence in oocytes after vitrification and warming? Design Mouse oocytes and four-cell embryos were vitrified and warmed with solutions supplemented with fatty acid and cultured to the blastocyst stage. To study lipid metabolism after vitrification, quantitative real-time polymerase chain reaction was used to analyse the expression of genes related to beta oxidation in mouse embryos vitrified and warmed with or without fatty acids. The effects of fatty acid supplementation in the warming solutions on the developmental competence of bovine and human embryos were analysed. Blastocyst outgrowth assay was used to evaluate the potential of human blastocysts for adhesion to fibronectin. Results The neutral lipid content of mouse oocytes in the fatty acid 1% supplementation group was significantly higher than in the fatty acid 0% group (P = 0.0032). The developmental rate to the blastocyst stage was significantly higher in the fatty acid 1% group than in the fatty acid 0% group in mice (P = 0.0345). Fatty acid supplementation in warming solution upregulated Acaa2 and Hadha in mouse embryos. Fatty acids significantly improved the developmental ability of bovine embryos to the blastocyst stage (P = 0.0048). Warming with 1% fatty acid supplementation significantly increased the proportion of human blastocysts with morphological grade A inner cell mass (P = 0.0074) and trophectoderm (P = 0.0323). Conclusions Fatty acid supplementation in the warming solutions improved the developmental competence of vitrified–warmed mouse oocytes by activating the beta-oxidation pathway. Fatty acid supplementation enhanced the developmental rate of bovine embryos to the blastocyst stage and improved morphological characteristics of human embryos vitrified at the cleavage stage.
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