Abstract

Meiotic maturation of mammalian oocytes is a precisely orchestrated and complex process. Dimethyl sulfoxide (DMSO), a widely used solvent, drug, and cryoprotectant, is capable of disturbing asymmetric cytokinesis of oocyte meiosis in mice. However, in pigs, DMSO’s effect on oocyte meiosis still remains unknown. We aimed to evaluate if DMSO treatment will affect porcine oocyte meiosis and the underlying molecular changes as well. Interestingly, we did not observe the formation of the large first polar body and symmetric division for porcine oocytes treated with DMSO, contrary to findings reported in mice. 3% DMSO treatment could inhibit cumulus expansion, increase nuclear abnormality, disturb spindle organization, decrease reactive oxygen species level, and elevate mitochondrial membrane potential of porcine oocytes. There was no effect on germinal vesicle breakdown rate regardless of DMSO concentration. 3% DMSO treatment did not affect expression of genes involved in spindle organization (Bub1 and Mad2) and apoptosis (NF-κB, Pten, Bcl2, Caspase3 and Caspase9), however, it significantly decreased expression levels of pluripotency genes (Oct4, Sox2 and Lin28) in mature oocytes. Therefore, we demonstrated that disturbed cumulus expansion, chromosome alignment, spindle organization and pluripotency gene expression could be responsible for DMSO-induced porcine oocyte meiotic arrest and the lower capacity of subsequent embryo development. Our results provide new insights on DMSO’s effect on porcine oocyte meiosis and raise safety concerns over DMSO’s usage on female reproduction in both farm animals and humans.

Highlights

  • Meiotic maturation of mammalian oocytes is a complex process precisely orchestrated by a wide array of endocrinal and molecular cues [1]

  • When we analyzed the 3% Dimethyl sulfoxide (DMSO) treatment on cumulus expansion in detail, relative indices of cumulus expansion were found to be without significant changes during the entire process of in vitro maturation (IVM) (1.16 at 24h, 1.22 at 44h versus 1.0 at 0h, Fig 1, p > 0.05), showing different change dynamics as compared to the control group

  • When further compared the two groups at different time points, we found that cumulus expansion at 24h of IVM in 3% DMSO treatment group (n = 150) was significantly inhibited (1.16 versus 2.52) (p < 0.05), while there were not different at 44h of IVM (1.28 and 1.22, p > 0.05)

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Summary

Introduction

Meiotic maturation of mammalian oocytes is a complex process precisely orchestrated by a wide array of endocrinal and molecular cues [1]. The successful completion of meiosis and embryo development depends on a number of important factors, for instance, the correct chromosome alignment and segregation via the bipolar spindle [5], which is formed by microtubules, a cytoskeletal structure important for the extrusion of polar bodies. The extrusion of the first polar body indicates the status of nuclear maturation, while the reactive oxygen species (ROS) level, activity and distribution of ooplasmic mitochondria reflect the quality of cytoplasmic maturation [7]. If both nuclear and cytoplasmic maturation are well coordinated and synchronized, oocyte will be of better quality, and embryos subsequently formed will have better developmental competence

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