Toumadje Arazdordi, Kusumoto Ken-Ichi, Parton Angela, Mericko Patricia, Dowell Lori, Ma Guozhong, Chen Luping, Barnes David W, Sato J Denry
National Stem Cell Resource, American Type Culture Collection, 10801 University Boulevard, Manassas, Virginia 20110, USA.
In Vitro Cell Dev Biol Anim. 2003 Nov-Dec;39(10):449-53. doi: 10.1290/1543-706X(2003)039<0449:PDIVOM>2.0.CO;2.
Although the ES-D3 murine embryonic stem cell line was one of the first derived, little information exists on the in vitro differentiation potential of these cells. We have used immunocytochemical and flow cytometric methods to monitor ES-D3 embryoid body differentiation in vitro during a 21-d period. Spontaneous differentiation of embryoid body cells was induced by leukemia inhibitory factor withdrawal in the absence of feeder cells. The pluripotent stem cell markers Oct-3/4, SSEA-1, and EMA-1 were found to persist for at least 7 d, whereas the primitive endoderm marker cytokeratin endo-A was expressed at increasing levels from day 6. The localization of these antigens within the embryoid bodies suggested that embryonic ectoderm- and primitive endoderm-derived tissues were segregated. Localized expression of class III beta-tubulin and sarcomeric myosin also was detected, indicating that representatives of all three embryonic germ layers were present after induction of differentiation in vitro.
尽管ES-D3小鼠胚胎干细胞系是最早获得的细胞系之一,但关于这些细胞的体外分化潜能的信息却很少。我们使用免疫细胞化学和流式细胞术方法,在21天的时间内监测ES-D3胚状体在体外的分化情况。在没有饲养层细胞的情况下,通过撤除白血病抑制因子来诱导胚状体细胞的自发分化。发现多能干细胞标志物Oct-3/4、SSEA-1和EMA-1至少持续存在7天,而原始内胚层标志物细胞角蛋白endo-A从第6天开始表达水平不断增加。这些抗原在胚状体内的定位表明,胚胎外胚层和原始内胚层来源的组织是分离的。还检测到III类β-微管蛋白和肌节肌球蛋白的定位表达,表明在体外诱导分化后,所有三个胚胎胚层的代表都存在。