Improved Murine Blastocyst Quality and Development in a Single Culture Medium Compared to Sequential Culture Media

Objective: Validate single versus sequential culture media for murine embryo development. Design: Prospective laboratory experiment. Setting: Assisted Reproduction Laboratory. Animals: Murine embryos. Interventions: Thawed murine zygotes cultured for 3 or 5 days (d3 or d5) in single or sequential em...

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Veröffentlicht in:Reproductive sciences (Thousand Oaks, Calif.) Calif.), 2016-03, Vol.23 (3), p.310-317
Hauptverfasser: Hennings, Justin M., Zimmer, Randall L., Nabli, Henda, Davis, J. Wade, Sutovsky, Peter, Sutovsky, Miriam, Sharpe-Timms, Kathy L.
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Sprache:eng
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Zusammenfassung:Objective: Validate single versus sequential culture media for murine embryo development. Design: Prospective laboratory experiment. Setting: Assisted Reproduction Laboratory. Animals: Murine embryos. Interventions: Thawed murine zygotes cultured for 3 or 5 days (d3 or d5) in single or sequential embryo culture media developed for human in vitro fertilization. Main Outcome Measures: On d3, zygotes developing to the 8 cell (8C) stage or greater were quantified using 4’,6-diamidino-2-phenylindole (DAPI), and quality was assessed by morphological analysis. On d5, the number of embryos reaching the blastocyst stage was counted. DAPI was used to quantify total nuclei and inner cell mass nuclei. Localization of ubiquitin C-terminal hydrolase L1 (UCHL1) and ubiquitin C-terminal hydrolase L3 (UCHL3) was reference points for evaluating cell quality. Results: Comparing outcomes in single versus to sequential media, the odds of embryos developing to the 8C stage on d3 were 2.34 time greater (P = .06). On d5, more embryos reached the blastocyst stage (P =
ISSN:1933-7191
1933-7205
DOI:10.1177/1933719115618281