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优化培养保存方法以维持猪体外成熟(IVM)后的中期II(MII)卵母细胞的发育能力。

Optimization of culture-preservation methods to maintain developmental competence in porcine metaphase II (MII) oocytes post-in vitro maturation (IVM).

作者信息

Tsuji Haruhisa, Maeyama Rei, Kato Yoko

机构信息

Laboratory of Animal Reproduction, College of Agriculture, Kindai University, 3327-204, Nakamachi, Nara 631-8505, Japan.

出版信息

Exp Anim. 2025 Apr 20;74(2):189-196. doi: 10.1538/expanim.24-0107. Epub 2024 Nov 29.

Abstract

After in vitro maturation (IVM) of porcine germinal vesicle (GV) oocytes, those that matured to the metaphase II (MII) stage were selected for further culture over a period of 24-48 h. Subsequently, these oocytes were either parthenogenetically activated or used for somatic cell nuclear transfer (SCNT) to evaluate their in vitro developmental competence. Parthenogenetically activated MII oocytes developed to the blastocyst stage after 42 h of continuous culture, whereas SCNT oocytes reached the blastocyst stage within 30 h of culture. These findings suggest that porcine MII oocytes retain their developmental competence after extended in vitro culture exceeding 30 h. This study highlights the potential of prolonged culture in enhancing the utility of MII-stage oocytes for livestock applications and possibly for future advancements in human infertility treatments.

摘要

猪生发泡(GV)卵母细胞经体外成熟(IVM)后,选择那些成熟至中期 II(MII)阶段的卵母细胞进行为期24 - 48小时的进一步培养。随后,这些卵母细胞要么进行孤雌激活,要么用于体细胞核移植(SCNT),以评估它们的体外发育能力。孤雌激活的MII卵母细胞在连续培养42小时后发育至囊胚阶段,而SCNT卵母细胞在培养30小时内达到囊胚阶段。这些发现表明,猪MII卵母细胞在体外延长培养超过30小时后仍保留其发育能力。本研究强调了延长培养在提高MII期卵母细胞在畜牧应用中的效用以及可能在未来人类不孕症治疗进展方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7fb/12044358/3675034d0974/expanim-74-189-g001.jpg

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