4.7 Article

Enhancing Oocyte Competence With Milrinone as a Phosphodiesterase 3A Inhibitor to Improve the Development of Porcine Cloned Embryos

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2021.647616

Keywords

oocyte; cloning; development; meiosis; milrinone

Funding

  1. Korea Health Technology R&D Project through the Korea Health Industry Development Institute - Ministry of Health and Welfare of South Korea [HI13C0954]

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The study investigated the effect of milrinone supplementation during in vitro maturation on porcine oocytes and cloned embryo development. Results showed that milrinone improved maturation and blastocyst development rates in less competent oocytes, potentially due to coordinated cytoplasmic and nuclear maturation. Milrinone supplementation also led to higher expression levels of reprogramming-related genes in oocytes, indicating its usefulness for proper nuclear reprogramming in cloned embryo production.
The objective of this study was to investigate the effect of milrinone supplementation as a phosphodiesterase 3A inhibitor during in vitro maturation (IVM) to coordinate the cytoplasmic and nuclear maturation of porcine oocytes and subsequent development of porcine cloned embryos. Brilliant cresyl blue (BCB)-stained (BCB +) oocytes, classified as well-developed, and BCB- oocytes were used in parthenogenesis (PA) and cloning, and their preimplantation development was compared. In PA embryos, BCB + oocytes had significantly higher rates of development than BCB- oocytes in terms of maturation (87.5 vs. 71.3%), cleavage (88.6 vs. 76.3%), and blastocyst development (34.3 vs. 25.3%) and also had higher cell numbers (46.9 vs. 38.9%), respectively (p < 0.05). In cloned embryos, the BCB + group also had a significantly higher blastocyst formation rate than the BCB- group (30.6 vs. 20.1%; p < 0.05). Supplementation with 75 mu M milrinone during IVM of BCB- oocytes showed improvement in maturation and blastocyst development rates, which may be due to the coordinated maturation of the cytoplasm with the nucleus as an effect of milrinone. Moreover, the analysis of nuclear reprogramming via the examination of the expression levels of the reprogramming-related genes POU5F1, DPPA2, and NDP52IL in milrinone-supplemented BCB- oocytes showed higher expression levels than that in non-treated BCB- oocytes. These findings demonstrate that milrinone is useful in improving developmental competence in less competent oocytes during IVM and for proper nuclear reprogramming in the production of porcine cloned embryos by coordinating cytoplasmic and nucleus maturation.

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