Dráber P, Nosek J, Pokorná Z
Department of Developmental Genetics, Czechoslovak Academy of Sciences, Prague.
Proc Natl Acad Sci U S A. 1989 Dec;86(23):9337-41. doi: 10.1073/pnas.86.23.9337.
Most developmentally regulated epitopes identified on embryonal carcinoma cells and murine preimplantation embryos are associated with a glycoprotein-bound large glycan called embryoglycan. To prepare monoclonal antibodies recognizing other, less immunogenic stage-specific embryonic epitopes, we used embryoglycan-negative embryonal carcinoma cells P19XT.1.1 as immunogen. One monoclonal antibody prepared by this strategy was found to react specifically with mouse embryonal carcinoma and embryo-derived stem cell lines. The target epitope, TEC-4, was found to be expressed on eggs and two-cell embryos but was undetectable on later stages of mouse embryos and adult mouse tissues. NaDodSO4/PAGE of immunoaffinity-isolated antigen revealed that TEC-4 epitope is associated with glycoproteins of apparent Mr 120,000 and 240,000. The epitope was resistant to oxidation by sodium periodate and to digestion by endoglycosidase F but was sensitive to treatment with protein-denaturing agents and proteases, which suggested that the epitope is located in the protein moiety of the molecule. In the course of retinoic acid-induced differentiation of embryonal carcinoma cells the epitope disappeared before the onset of morphological differentiation. The combined data indicate that TEC-4 is an unusual stage-specific embryonic antigen that may be amenable to direct genetic analysis.
在胚胎癌细胞和小鼠植入前胚胎上鉴定出的大多数发育调控表位都与一种名为胚胎聚糖的糖蛋白结合型大聚糖有关。为了制备能够识别其他免疫原性较低的阶段特异性胚胎表位的单克隆抗体,我们使用胚胎聚糖阴性的胚胎癌细胞P19XT.1.1作为免疫原。通过这种策略制备的一种单克隆抗体被发现能与小鼠胚胎癌和胚胎衍生的干细胞系发生特异性反应。发现靶表位TEC-4在卵子和二细胞胚胎上表达,但在小鼠胚胎后期和成年小鼠组织中无法检测到。免疫亲和分离抗原的十二烷基硫酸钠/聚丙烯酰胺凝胶电泳显示,TEC-4表位与表观分子量为120,000和240,000的糖蛋白有关。该表位对高碘酸钠氧化和内切糖苷酶F消化具有抗性,但对蛋白质变性剂和蛋白酶处理敏感,这表明该表位位于分子的蛋白质部分。在胚胎癌细胞视黄酸诱导分化过程中,该表位在形态分化开始前消失。综合数据表明,TEC-4是一种不寻常的阶段特异性胚胎抗原,可能适合直接进行基因分析。