Institute of Agrobiological Sciences, National Agriculture and Food Research Organization, Tsukuba, Ibaraki, Japan.
PLoS One. 2023 Mar 17;18(3):e0282959. doi: 10.1371/journal.pone.0282959. eCollection 2023.
The present study investigated the effects of vitrification of porcine oocytes either at the immature Germinal Vesicle (GV) stage before in vitro maturation (GV-stage oocytes) or at the pronuclear stage after in vitro maturation and fertilization (zygotes) on DNA integrity in relevance with their subsequent embryo development. Vitrification at the GV stage but not at the pronuclear stage significantly increased the abundance of double-strand breaks (DSBs) in the DNA measured by the relative fluorescence after γH2AX immunostaining. Treatment of GV-stage oocytes with cryoprotectant agents alone had no effect on DSB levels. When oocytes were vitrified at the GV stage and subjected to in vitro maturation and fertilization (Day 0) and embryo culture, significantly increased DSB levels were detected in subsequent cleavage-stage embryos which were associated with low cell numbers on Day 2, the upregulation of the RAD51 gene at the 4-8 cell stage (measured by RT-qPCR) and reduced developmental ability to the blastocyst stage when compared with the non-vitrified control. However, total cell numbers and percentages of apoptotic cells (measured by TUNEL) in resultant blastocysts were not different from those of the non-vitrified control. On the other hand, vitrification of zygotes had no effect on DSB levels and the expression of DNA-repair genes in resultant embryos, and their development did not differ from that of the non-vitrified control. These results indicate that during vitrification GV-stage oocytes are more susceptible to DNA damages than zygotes, which affects their subsequent development to the blastocyst stage.
本研究调查了玻璃化冷冻在不成熟的生发泡期(GV 期)的猪卵母细胞(GV 期卵母细胞)或体外成熟和受精后的原核期(受精卵)对 DNA 完整性的影响,以及与后续胚胎发育的关系。GV 期的玻璃化冷冻而非原核期的玻璃化冷冻显著增加了 γH2AX 免疫染色后相对荧光测定的 DNA 双链断裂(DSB)的丰度。单独用冷冻保护剂处理 GV 期卵母细胞对 DSB 水平没有影响。当 GV 期卵母细胞进行玻璃化冷冻并进行体外成熟和受精(第 0 天)以及胚胎培养时,在随后的卵裂期胚胎中检测到明显增加的 DSB 水平,这些胚胎在第 2 天的细胞数量较少,RAD51 基因在 4-8 细胞阶段的上调(通过 RT-qPCR 测量),并且与非玻璃化冷冻对照组相比,发育能力降低到囊胚阶段。然而,在玻璃化冷冻组中,囊胚的总细胞数和凋亡细胞的百分比(通过 TUNEL 测量)与非玻璃化冷冻对照组没有差异。另一方面,受精卵的玻璃化冷冻对 DSB 水平和 DNA 修复基因在胚胎中的表达没有影响,其发育与非玻璃化冷冻对照组没有差异。这些结果表明,在玻璃化冷冻过程中,GV 期卵母细胞比受精卵更容易受到 DNA 损伤的影响,这会影响它们随后发育到囊胚阶段。