Salvador Lisa M, Silva Celso P, Kostetskii Igor, Radice Glenn L, Strauss Jerome F
Center for Research on Reproduction and Women's Health, University of Pennsylvania Medical School, Philadelphia, PA 19104, USA.
Methods. 2008 Jun;45(2):172-81. doi: 10.1016/j.ymeth.2008.03.004. Epub 2008 May 29.
The study of germ cell-specific gene regulation in vitro is challenging. Here we report that the promoter of the oocyte-specific gene, Gdf9, is active in a population of cultured murine embryonic stem cells (ES) which have a phenotype resembling oocytes. The promoter region of the murine Gdf9 coupled to enhanced green fluorescent protein (eGFP) was stably transfected into XX mouse ES cells. eGFP was expressed only in oocytes of chimeric mice generated from the transfected XX ES cells. The transfected ES cells were examined when cultured on feeder layers or as embryoid bodies. Large eGFP-positive cells, surrounded by a structure resembling a zona pellucida appeared transiently in cultures of the ES cells on feeder layers. Surprisingly, they were detectable on days 1 and 2 of culture but virtually absent on day 3. Addition of leukemia inhibitory factor (LIF) to the media significantly increased the number of eGFP-positive cels resembling oocytes. Quantitative-time PCR demonstrated a parallel increase in Gdf9 and Zp3 mRNA with changes in the abundance of eGFP-positive cells. In embryoid body cultures, eGFP-positive cells appeared transiently and then re-appeared in regional clusters after 30-45 days of culture. These findings demonstrate that a population of cultured murine ES cells contain the transcriptional machinery to drive expression of an oocyte-specific gene, and that those cells phenotypically resemble oocytes.
体外研究生殖细胞特异性基因调控具有挑战性。在此我们报告,卵母细胞特异性基因Gdf9的启动子在一群培养的小鼠胚胎干细胞(ES细胞)中具有活性,这些细胞具有类似卵母细胞的表型。将与增强型绿色荧光蛋白(eGFP)偶联的小鼠Gdf9启动子区域稳定转染到XX小鼠ES细胞中。eGFP仅在由转染的XX ES细胞产生的嵌合小鼠的卵母细胞中表达。在饲养层上培养或作为胚状体培养时,对转染的ES细胞进行检测。在饲养层上培养的ES细胞中,大的eGFP阳性细胞被类似透明带的结构包围,短暂出现。令人惊讶的是,它们在培养的第1天和第2天可检测到,但在第3天几乎不存在。向培养基中添加白血病抑制因子(LIF)可显著增加类似卵母细胞的eGFP阳性细胞数量。定量实时PCR显示,随着eGFP阳性细胞丰度的变化,Gdf9和Zp3 mRNA平行增加。在胚状体培养中,eGFP阳性细胞短暂出现,然后在培养30 - 45天后在区域簇中再次出现。这些发现表明,一群培养的小鼠ES细胞含有驱动卵母细胞特异性基因表达的转录机制,并且这些细胞在表型上类似卵母细胞。