Ohta Hiroshi, Sakaide Yuko, Yamagata Kazuo, Wakayama Teruhiko
Laboratory for Genomic Reprogramming, Center for Developmental Biology, RIKEN, Kobe, Japan.
Biol Reprod. 2008 Sep;79(3):486-92. doi: 10.1095/biolreprod.107.067116. Epub 2008 May 7.
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.
四倍体(4n)胚胎互补试验表明,仅胚胎干细胞(ES细胞)就能支持胚胎发育(ES小鼠),从而能够直接从培养的ES细胞系中获得小鼠品系。尽管这项技术的优势已得到充分认可,但生成ES小鼠的效率仍然很低。在本研究中,我们调查了宿主4n胚胎的细胞数量对ES小鼠产生的影响。使用了四个独立的ES细胞系(两个普通ES细胞系和两个核移植衍生的ES细胞系),每个细胞系与单个(1X)至三个(3X)宿主4n胚胎聚集。我们发现,无论细胞系如何,使用1X 4n胚胎的ES小鼠出生率都相当低(0-2%),而在3X 4n胚胎的情况下,除了一个细胞系外,约6-14%的胚胎发育至足月。ES小鼠中宿主4n细胞的污染非常罕见,即使它们来自3X 4n宿主胚胎,其污染情况与使用常规方法产生的污染相当。这些结果表明,使用3X 4n胚胎对生成ES小鼠是有效的。我们在此描述的技术将适用于任何ES细胞系,包括用于基因靶向的普通ES细胞系。