Two-phase chemically defined culture system for preimplantation rat embryos

Yue Zhou, Vasiliy Galat, Ray Garton, Greg Taborn, Koji Niwa, Philip Iannaccone*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

A limiting factor in the development of new technologies and transport of rats worldwide has been the inability to robustly culture preimplantation embryos. Previously, culture in vitro to the blastocyst stage from one-cell embryos was successful only if the one-cell embryos were isolated near the time of the first cleavage and from only a few strains. Here we report the use of commonly available, chemically defined culture media to overcome these limitations. In vitro culture of young one-cell embryos using common embryo media (KSOM, BMOC, or HTF) for 18-22 h followed by culture in mR1ECM medium allows the successful in vitro development of blastocysts from one-cell embryos after 5 days from both outbred (SD) and inbred strains of rat (WF, LEW, F344, and PVG). This system allows the parthenogenetic development of chemically activated, unfertilized oocytes to the blastocyst stage. Embryos cultured in this system develop to term and are live-born following transfer to surrogate mothers.

Original languageEnglish (US)
Pages (from-to)129-133
Number of pages5
JournalGenesis
Volume36
Issue number3
DOIs
StatePublished - Jul 1 2003

Keywords

  • Culture system
  • In vitro development
  • Preimplantation
  • Rat embryos

ASJC Scopus subject areas

  • Genetics
  • Endocrinology
  • Cell Biology

Fingerprint

Dive into the research topics of 'Two-phase chemically defined culture system for preimplantation rat embryos'. Together they form a unique fingerprint.

Cite this