» Articles » PMID: 24328022

The Influence of Serum Substituents on Serum-free Vero Cell Conditioned Culture Media Manufactured from Dulbecco's Modified Eagle Medium in Mouse Embryo Culture

Overview
Date 2013 Dec 12
PMID 24328022
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: This study was conducted to examine the influences of supplementation of the serum substituents and available period of serum-free Vero cell conditioned media (SF-VCM) manufactured from Dulbecco's modified Eagle medium cultured with Vero cells for in vitro development of mouse preimplantation embryos.

Methods: A total of 1,099 two-cell embryos collected from imprinting control region mice were cultured in SF-VCM with 10% and 20% human follicular fluid (hFF), serum substitute supplement (SSS), and serum protein substitute (SPS). Development of embryos was observed every 24 hours. Results between different groups were analyzed by chi-square test, and considered statistically significant when P-value was less than 0.05.

Results: The rates of embryonic development cultured in SF-VCM supplemented with serum substituents were significantly higher compare with serum-free group (P < 0.05). The rates of embryonic development after 48 hours (morula≤) and 96 hours (blastocyst≤) were significantly higher in 20% SSS and 10% SPS than in 20% hFF supplementation (P < 0.05). And the rates of embryonic development after 96 hours (hatching blastocyst≤) were significantly higher in 10% SPS (94.5%) than in 20% SSS (82.6%) and 20% hFF supplementation (68.5%). The rates of embryonic development according to storage period of the SF-VCM supplemented with 10% SPS showed no significant difference between control, 2 weeks and 4 weeks group. However developmental rate in 6 weeks storage group was significantly lower than other groups.

Conclusion: The rate of embryonic development after 96 hours (hatching blastocyst≤) was significantly higher in SF-VCM supplemented with 10% SPS. And storage period of media up to 4 weeks did not affect on embryonic development.

References
1.
SCOTT L, Sundaram S, Smith S . The relevance and use of mouse embryo bioassays for quality control in an assisted reproductive technology program. Fertil Steril. 1993; 60(3):559-68. DOI: 10.1016/s0015-0282(16)56176-7. View

2.
Gardner D, Lane M, Stevens J, Schoolcraft W . Noninvasive assessment of human embryo nutrient consumption as a measure of developmental potential. Fertil Steril. 2001; 76(6):1175-80. DOI: 10.1016/s0015-0282(01)02888-6. View

3.
Takahashi Y, First N . In vitro development of bovine one-cell embryos: Influence of glucose, lactate, pyruvate, amino acids and vitamins. Theriogenology. 1992; 37(5):963-78. DOI: 10.1016/0093-691x(92)90096-a. View

4.
Fukui Y, McGowan L, James R, Pugh P, Tervit H . Factors affecting the in-vitro development to blastocysts of bovine oocytes matured and fertilized in vitro. J Reprod Fertil. 1991; 92(1):125-31. DOI: 10.1530/jrf.0.0920125. View

5.
Quinn P, Moinipanah R, Steinberg J, Weathersbee P . Successful human in vitro fertilization using a modified human tubal fluid medium lacking glucose and phosphate ions. Fertil Steril. 1995; 63(4):922-4. DOI: 10.1016/s0015-0282(16)57504-9. View