West J D, Flockhart J H, Keighren M
Department of Obstetrics and Gynaecology, University of Edinburgh, United Kingdom.
Dev Biol. 1995 Mar;168(1):76-85. doi: 10.1006/dbio.1995.1062.
Eight series of mouse chimeras were produced by aggregating 8-cell embryos that differed at the Gpi-1s locus, encoding glucose phosphate isomerase (GPI-1). Chimeric blastocysts (Gpi-1sa/Gpi-1sa <--> Gpi-1sb/Gpi-1sb) were transferred to pseudopregnant females, which produced only GPI-1C enzyme. Quantitative electrophoresis of GPI-1 was used to estimate the contribution of each embryo (GPI-1A and GPI-1B enzyme activity) to the fetus and placentas of 12 1/2 day chimeric conceptuses. Chimeric fetuses and placentas were identified by the presence of both GPI-1AA and GPI-1BB homodimers. The overall distribution of the percentage GPI-1A in the placentas was bimodal or U-shaped. It was positively correlated with the %GPI-1A in the fetus in most of the eight series of chimeras analyzed. In the first chimera experiment, involving seven series of chimeras, GPI-1AB heteropolymer was detected in 78/211 (37%) of the placentas. Heteropolymer was not detected in chimeric placentas with an unbalanced composition of GPI-1A and GPI-1B. The production of heteropolymer implies that GPI-1A and GPI-1B monomers are produced in the same cell and that fusion must have occurred between the two genetically distinct cell populations in the placenta. In the second experiment, samples of different regions were dissected from another series of 27 chimeric placentas and analyzed; 12 contained heteropolymer. Although GPI-1AB heteropolymer was widely distributed throughout the placenta it was detected less frequently in the outer part of the placenta. In another experiment, analysis of 34 homozygous (nonchimeric) Gpi-1sb/Gpi-1sb conceptuses transferred to homozygous Gpi-1sa/Gpi-1sa reproductive tracts revealed no evidence for fusion between maternal cells and cells of zygotic origin in the placenta. The chimera studies provide biochemical evidence for fusion between zygotic cells in the murine placenta. This presumably occurs during the formation of the syncytial trophoblast.
通过聚合在编码葡萄糖磷酸异构酶(GPI-1)的Gpi-1s位点存在差异的8细胞胚胎,产生了8组小鼠嵌合体。将嵌合胚泡(Gpi-1sa/Gpi-1sa <--> Gpi-1sb/Gpi-1sb)移植到假孕雌性体内,这些雌性只产生GPI-1C酶。利用GPI-1的定量电泳来估计每个胚胎(GPI-1A和GPI-1B酶活性)对12.5天大的嵌合胚胎的胎儿和胎盘的贡献。通过同时存在GPI-1AA和GPI-1BB同型二聚体来鉴定嵌合胎儿和胎盘。胎盘中GPI-1A百分比的总体分布是双峰或U形的。在分析的八组嵌合体中的大多数中,它与胎儿中的GPI-1A百分比呈正相关。在第一个嵌合体实验中,涉及七组嵌合体,在78/211(37%)的胎盘中检测到GPI-1AB杂聚物。在GPI-1A和GPI-1B组成不平衡的嵌合胎盘中未检测到杂聚物。杂聚物的产生意味着GPI-1A和GPI-1B单体在同一细胞中产生,并且胎盘内两个基因不同的细胞群体之间一定发生了融合。在第二个实验中,从另一组27个嵌合胎盘中解剖出不同区域的样本并进行分析;12个含有杂聚物。尽管GPI-1AB杂聚物广泛分布于整个胎盘,但在胎盘外部检测到的频率较低。在另一个实验中,对移植到纯合Gpi-1sa/Gpi-1sa生殖道中的34个纯合(非嵌合)Gpi-1sb/Gpi-1sb胚胎的分析显示,没有证据表明胎盘母体细胞与合子来源细胞之间发生融合。嵌合体研究为小鼠胎盘合子细胞之间的融合提供了生化证据。这大概发生在合体滋养层形成期间。