Clin Exp Reprod Med.  2023 Dec;50(4):244-252. 10.5653/cerm.2023.06436.

Enhancement of preimplantation mouse embryo development with optimized in vitro culture dish via stabilization of medium osmolarity

Affiliations
  • 1Department of Senior Healthcare, Graduate School of Eulji University, Seongnam, Republic of Korea
  • 2CNC Biotech Incorporated, Suwon, Republic of Korea
  • 3Department of Biomedical Laboratory Science, Graduate School of Eulji University, Seongnam, Republic of Korea
  • 4Department of Biomedical Laboratory Science, College of Health Science, Eulji University, Seongnam, Republic of Korea

Abstract


Objective
We evaluated the efficacy of the newly developed optimized in vitro culture (OIVC) dish for cultivating preimplantation mouse embryos. This dish minimizes the need for mineral oil and incorporates microwells, providing a stable culture environment and enabling independent monitoring of individual embryos.
Methods
Mouse pronuclear (PN) zygotes and two-cell-stage embryos were collected at 18 and 46 hours after human chorionic gonadotropin injection, respectively. These were cultured for 120 hours using potassium simplex optimized medium (KSOM) to reach the blastocyst stage. The embryos were randomly allocated into three groups, each cultured in one of three dishes: a 60-mm culture dish, a microdrop dish, and an OIVC dish that we developed.
Results
The OIVC dish effectively maintained the osmolarity of the KSOM culture medium over a 5-day period using only 2 mL of mineral oil. This contrasts with the significant osmolarity increase observed in the 60-mm culture dish. Additionally, the OIVC dish exhibited higher blastulation rates from two-cell embryos (100%) relative to the other dish types. Moreover, blastocysts derived from both PN zygotes and two-cell embryos in the OIVC dish group demonstrated significantly elevated mean cell numbers.
Conclusion
Use of the OIVC dish markedly increased the number of cells in blastocysts derived from the in vitro culture of preimplantation mouse embryos. The capacity of this dish to maintain medium osmolarity with minimal mineral oil usage represents a breakthrough that may advance embryo culture techniques for various mammals, including human in vitro fertilization and embryo transfer programs.

Keyword

Blastulation; Cell count; In vitro culture; Mineral oil; Optimized in vitro culture dish; Osmolar concentration
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