Wang Zhongde, Jaenisch Rudolf
Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Dev Biol. 2004 Nov 1;275(1):192-201. doi: 10.1016/j.ydbio.2004.06.026.
Chimeric or entirely embryonic stem (ES) cell-derived mice ("ES mice") can be produced by injecting ES cells into diploid (2n) or tetraploid (4n) host blastocysts, respectively. Usually, between 10 and 15 ES cells are injected into the host blastocyst, but it is not clear how many of the injected cells contribute to the somatic lineages, thus serve as "founder cells" of the embryo proper. We have used genetically labeled ES cells to retrospectively determine the number of founder ES cells that generate the somatic lineages of chimeric and of ES mice. ES cell clones individually labeled with provirus were mixed in equal numbers and injected into 2n or 4n blastocysts to generate chimeric or ES mice. Southern analysis of DNA from the resulting animals indicated that the somatic lineages were most often derived from one or two and sometimes from up to three founder ES cells. The number of founder cells was independent of the total number of cells injected into the host blastocysts. Our results are consistent with the notion that constraints of the host embryo restrict the number of ES cells that can contribute to a chimeric or an ES mouse.
嵌合小鼠或完全由胚胎干细胞(ES细胞)衍生而来的小鼠(“ES小鼠”)可分别通过将ES细胞注射到二倍体(2n)或四倍体(4n)宿主囊胚中产生。通常,会将10到15个ES细胞注射到宿主囊胚中,但尚不清楚注射的细胞中有多少会对体细胞谱系产生贡献,从而成为胚胎本身的“奠基细胞”。我们利用基因标记的ES细胞来追溯性地确定产生嵌合小鼠和ES小鼠体细胞谱系的奠基ES细胞数量。用前病毒单独标记的ES细胞克隆以相等数量混合,然后注射到2n或4n囊胚中以产生嵌合小鼠或ES小鼠。对所得动物的DNA进行Southern分析表明,体细胞谱系最常源自一两个,有时多达三个奠基ES细胞。奠基细胞的数量与注射到宿主囊胚中的细胞总数无关。我们的结果与宿主胚胎的限制会限制可对嵌合小鼠或ES小鼠产生贡献的ES细胞数量这一观点一致。