Luciano Alberto M, Franciosi Federica, Barros Rodrigo G, Dieci Cecilia, Lodde Valentina
Reproductive and Developmental Biology Laboratory, Department of Health, Animal Science and Food Safety, University of Milan, 20133 Milan, Italy.
Anim Reprod. 2018 Aug 3;15(Suppl 1):727-736. doi: 10.21451/1984-3143-AR2018-0021. eCollection 2018 Jul-Sep.
The efficiency of assisted reproductive technologies, consisting of the transfer of embryos obtained through maturation, fertilization and early embryo culture is still limited. The quality of the oocytes is pivotal for assisted reproductive efficiency and the maturation of the oocyte represents the first key limiting step of the embryo production system. At the time of removal from the antral follicles, the oocyte is still completing the final growth and differentiation steps, needed to provide the so-called developmental competence, i.e. the machinery required to sustain fertilization and embryo development. In mono-ovular species only one oocyte per cycle is available for procreation, therefore the current assisted reproduction techniques strive to overcome this natural boundary. However, the success is still limited and overall the effectiveness does not exceed the efficiency achieved in millions of years of mammalian evolution. One of the problems lies in the intrinsic heterogeneity of the oocytes that are subjected to maturation and in the lack of dedicated approaches to finalize the differentiation process. In this review we will try to overview some of the salient aspects of current practices by emphasizing the most critical and fundamental features in oocyte differentiation that should be carefully considered for improving current techniques.
辅助生殖技术的效率仍然有限,该技术包括通过卵子成熟、受精和早期胚胎培养获得的胚胎移植。卵母细胞的质量对于辅助生殖效率至关重要,而卵母细胞的成熟是胚胎生产系统的第一个关键限制步骤。从窦卵泡中取出时,卵母细胞仍在完成最终的生长和分化步骤,以提供所谓的发育能力,即维持受精和胚胎发育所需的机制。在单胎物种中,每个周期只有一个卵母细胞可用于繁殖,因此当前的辅助生殖技术努力克服这一自然限制。然而,成功率仍然有限,总体而言,其有效性并未超过数百万年哺乳动物进化所达到的效率。问题之一在于接受成熟的卵母细胞存在内在异质性,且缺乏专门的方法来完成分化过程。在这篇综述中,我们将试图概述当前实践的一些显著方面,强调卵母细胞分化中最关键和基本的特征,这些特征对于改进当前技术应予以仔细考虑。
Anim Reprod. 2018-8-3
Hum Reprod Update. 2018-5-1
Biol Reprod. 2018-2-1
Results Probl Cell Differ. 2017
Reproduction. 2016-11