Maintenance of developmental competence in feline oocytes following 24 h of meiotic arrest with physiological agents.

IF 2.1
Shelley E S Sandmaier, Jason R Herrick
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Abstract

Context In vitro matured (IVM) feline oocytes exhibit reduced developmental competence compared to in vivo matured oocytes. Aims Arresting meiosis prior to IVM (pre-IVM) has been shown to improve oocyte quality in other species. Methods Cumulus-oocyte complexes (COCs) from domestic cats were matured in vitro immediately after collection or following 24h of pre-IVM. Following IVF, embryonic development was evaluated. Key results Embryonic cleavage, development to blastocyst, and hatching were not different (P >0.05) for oocytes subjected to meiotic arrest compared to control oocytes. Gene expression of pluripotency markers and blastocyst cell numbers were also unchanged by the various pre-IVM supplements. Conclusions It is possible to maintain feline oocytes in culture for up to 24h without compromising developmental competence. Implications Further manipulation of the culture environment during this period of meiotic arrest could be a novel means of improving the quality of feline oocytes.

生理药物抑制减数分裂24小时后猫卵母细胞发育能力的维持。
与体内成熟卵母细胞相比,体外成熟(IVM)猫卵母细胞表现出较低的发育能力。目的在其他物种中,在IVM前阻止减数分裂(pre-IVM)已被证明可以改善卵母细胞质量。方法将家猫卵母细胞卵母细胞复合物(COCs)采集后立即体外成熟,或在预ivm 24h后体外成熟。体外受精后,对胚胎发育进行评估。关键结果减数分裂停止的卵母细胞与对照卵母细胞相比,胚胎分裂、囊胚发育和孵化均无差异(P < 0.05)。多能性标记物的基因表达和囊胚细胞数量也被各种预ivm补充物所改变。结论在不影响发育能力的情况下,培养猫卵母细胞可达24小时。在减数分裂停滞期间进一步操纵培养环境可能是提高猫卵母细胞质量的一种新手段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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