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Increasing the Cell Number of Host Tetraploid Embryos Can Improve the Production of Mice Derived from Embryonic Stem Cells¹

Laboratory for Genomic Reprogramming, Center for Developmental Biology, RIKEN, Kobe 650-0047, Japan

ABSTRACT

Tetraploid (4n) embryo complementation assay has shown that embryonic stem (ES) cells alone are capable of supporting embryonic development (ES mouse), allowing the recovery of mouse lines directly from cultured ES cell lines. Although the advantages of this technique are well recognized, it remains inefficient for generating ES mice. In the present study, we investigated the effects of cell number of host 4n embryos on the production of ES mice. Four independent ES cell lines (two general ES cell lines and two nuclear transfer-derived ES cell lines) were used, and each cell line was aggregated with single (1x) to triple (3x) host 4n embryos. We found that birth rate of ES mice using 1x 4n embryos was quite low (0–2%) regardless of cell line, whereas except for one cell line, approximately 6–14% of embryos developed to full term in the case of 3x 4n embryos. Contamination of host 4n cells in ES mice was quite rare, being comparable to that generated using general methods even if they were delivered from 3x 4n host embryos. These results demonstrate that the use of 3x 4n embryos is effective for generating ES mice. Our technique described here will be applicable to any ES cell line, including general ES cell lines used for gene targeting.

developmental biology, embryo, embryonic stem cells, ES mouse, tetraploid complementation assay, trophectoderm

¹ Supported by grants for Scientific Research in Priority Areas and the Project for the Realization of Regenerative Medicine (research field: technical development of stem cell manipulation) to T.W. by the Ministry of Education, Culture, Sports, Science, and Technology of Japan.

Correspondence: ²Hiroshi Ohta, Laboratory for Genomic Reprogramming, Center for Developmental Biology, RIKEN, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe 650-0047, Japan. FAX: 81 78 306 3095; e-mail: ohta{at}cdb.riken.jp