Department of Animal Biotechnology, NAIC-Agricultural Biotechnology Institute, Gödöllö, Hungary.
Department of Animal Biotechnology, NAIC-Agricultural Biotechnology Institute, Gödöllö, Hungary.
J Biotechnol. 2017 Oct 10;259:86-90. doi: 10.1016/j.jbiotec.2017.07.037. Epub 2017 Aug 1.
Lentiviral gene constructs can be efficiently and specifically delivered to trophoblast cell lineages in rodents. In vivo genetic manipulation of trophoblast cell lines enables functional and developmental studies in the placenta. In this report we show that genetic modification can be produced in the extraembryonic tissues of rabbits by lentiviral gene constructs. When 8-16 cell stage embryos were injected with lentiviral particles, strong reporter gene expression resulted in the rabbit placenta. The expression pattern displayed some mosaicism. A strikingly high degree of mosaic GFP expression was detected in some parts of the yolk sac, which is a hypoblast-derived tissue. Whereas expression of the reporter gene construct was detected in placentas and yolk sacs, fetuses never expressed the transgene. As rabbits are an ideal model for functional studies in the placenta, our method would open new possibilities in rabbit biotechnology and placentation studies.
慢病毒基因构建体可以有效地特异性递送到啮齿动物的滋养层细胞谱系中。在体内对滋养层细胞系进行遗传操作可以在胎盘内进行功能和发育研究。在本报告中,我们表明可以通过慢病毒基因构建体在兔的胚胎外组织中产生遗传修饰。当将慢病毒颗粒注射到 8-16 细胞阶段的胚胎中时,强烈的报告基因表达导致兔胎盘出现。表达模式显示出一些嵌合性。在蛋黄囊的某些部位检测到 GFP 表达的高度嵌合性,蛋黄囊是由下胚层衍生而来的组织。尽管在胎盘和蛋黄囊中检测到报告基因构建体的表达,但胎儿从未表达过转基因。由于兔子是胎盘功能研究的理想模型,我们的方法将为兔生物技术和胎盘研究开辟新的可能性。