| Affiliation: | (1) Department of Biochemistry and Molecular Biology, University of Texas M. D. Anderson Cancer Center Genetically Engineered Mouse Facility, 1515 Holcombe Blvd., Houston, Texas, USA;(2) Department of Molecular Genetics, University of Texas M. D. Anderson Cancer Center Genetically Engineered Mouse Facility, 1515 Holcombe Blvd., Houston, Texas, USA;(3) Department of Biostatistics and Applied Mathematics, University of Texas M. D. Anderson Cancer Center Genetically Engineered Mouse Facility, 1515 Holcombe Blvd., Houston, Texas, USA |
| Abstract: | The production of chimeric mice is a complex process, requiring the careful coordination of tissue culture cell growth, production of a large number (30–75) of competent blastocysts and the availability of appropriately timed pseudo pregnant female mice. Failure at any of these steps can impinge upon the rapid production of chimeras. One potential improvement for the efficient generation of chimeric mice would be the utilization of cryopreserved embryos suitable for injection. C57Bl/6 morulae were frozen using a standard 2-step protocol with ethylene glycol as the cryopreservation agent. We determined that cryopreserved morulae could thaw, culture to blastocyst stage in KSOM media and survive injection at rates equivalent to control embryos. Cryopreserved morulae were also equivalent to controls at all later stages in the process of production of chimeric mice, including birth rate, percentage chimerism of resulting animals and ability to produce germline progeny. Hence, cryopreservation of morulae for blastocyst injection is a suitable option to enhance the efficiency of chimeric mouse generation. |
