Brice E C, Wu J X, Muraro R, Adamson E D, Wiley L M
Department of Obstetrics and Gynecology, University of California, Davis 95616-8615.
Dev Genet. 1993;14(3):174-84. doi: 10.1002/dvg.1020140304.
Two-cell mouse preimplantation embryos were cultured for 48 h in four different reagents to modulate epidermal growth factor (EGF) receptor function. These were rabbit polyclonal and mouse monoclonal antibodies to EGF receptor, EGF receptor antisense RNA, and EGF receptor antisense deoxyoligonucleotides. Embryos were scored for two endpoints: onset of cavitation as a measure of trophectoderm differentiation and mean embryo cell number as a measure of cell proliferation. The consistent observations were that cavitation was significantly accelerated by antibodies and delayed by antisense RNA and antisense deoxyoligonucleotides. None of these reagents exerted a significant effect on mean embryo cell number, with one exception, the polyclonal antibody. Our interpretation of these observations is that the antibody binding facilitated cavitation by mimicking natural ligand-receptor binding and inducing the signal transduction cascade that is typical for the EGF receptor. In the case of antisense RNA or deoxyoligonucleotide, we propose that they delayed onset of cavitation by interfering with EGF receptor production. We hypothesize that during this period of development, EGF receptor is concerned predominantly with the regulation of differentiation more than with cell proliferation.
将二细胞期小鼠植入前胚胎在四种不同试剂中培养48小时,以调节表皮生长因子(EGF)受体功能。这些试剂分别是针对EGF受体的兔多克隆抗体和小鼠单克隆抗体、EGF受体反义RNA以及EGF受体反义脱氧寡核苷酸。对胚胎的两个终点进行评分:空泡化的开始作为滋养外胚层分化的指标,平均胚胎细胞数作为细胞增殖的指标。一致的观察结果是,抗体显著加速了空泡化,而反义RNA和反义脱氧寡核苷酸则延迟了空泡化。除多克隆抗体外,这些试剂均未对平均胚胎细胞数产生显著影响。我们对这些观察结果的解释是,抗体结合通过模拟天然配体-受体结合并诱导EGF受体典型的信号转导级联反应促进了空泡化。对于反义RNA或脱氧寡核苷酸,我们认为它们通过干扰EGF受体的产生延迟了空泡化的开始。我们假设在这个发育阶段,EGF受体主要参与分化的调节,而不是细胞增殖。