Advanced Maternal Age Affects the Cryosusceptibility of Ovulated but not In Vitro Matured Mouse Oocytes

Reprod Sci. 2024 May;31(5):1420-1428. doi: 10.1007/s43032-024-01462-6. Epub 2024 Jan 31.

Abstract

Oocyte cryopreservation is offered to women of various age groups for both health and social reasons. Oocytes derived from either controlled ovarian stimulation or in vitro maturation (IVM) are cryopreserved via vitrification. As maternal age is a significant determinant of oocyte quality, there is limited data on the age-related susceptibility of oocytes to the vitrification-warming procedure alone or in conjunction with IVM. In the present study, metaphase II oocytes obtained from 2, 6, 9, and 12 month old Swiss albino mice either by superovulation or IVM were used. To understand the association between maternal age and oocyte cryotolerance, oocytes were subjected to vitrification-warming and compared to non vitrified sibling oocytes. Survived oocytes were evaluated for mitochondrial potential, spindle integrity, relative expression of spindle checkpoint protein transcripts, and DNA double-strand breaks. Maturation potential and vitrification-warming survival were significantly affected (p < 0.001 and p < 0.05, respectively) in ovulated oocytes from the advanced age group but not in IVM oocytes. Although vitrification-warming significantly increased spindle abnormalities in ovulated oocytes from advanced maternal age (p < 0.01), no significant changes were observed in IVM oocytes. Furthermore, Bub1 and Mad2 transcript levels were significantly higher in vitrified-warmed IVM oocytes (p < 0.05). In conclusion, advanced maternal age can have a negative impact on the cryosusceptibility of ovulated oocytes but not IVM oocytes in mice.

Keywords: Assisted reproductive technology; Fertility preservation; In vitro maturation; Maternal age; Oocyte vitrification.

MeSH terms

  • Animals
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism
  • Cell Survival / physiology
  • Cryopreservation* / methods
  • DNA Breaks, Double-Stranded
  • Female
  • In Vitro Oocyte Maturation Techniques*
  • Mad2 Proteins / metabolism
  • Maternal Age*
  • Mice
  • Oocytes* / physiology
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • Spindle Apparatus / metabolism
  • Spindle Apparatus / physiology
  • Vitrification*

Substances

  • Mad2 Proteins
  • Mad2l1 protein, mouse
  • Bub1b protein, mouse
  • Protein Serine-Threonine Kinases
  • Cell Cycle Proteins