Liu A, Joyner A L, Turnbull D H
Skirball Institute of Biomolecular Medicine, New York University Medical Center, 540 First Avenue, New York, NY 10016, USA.
Mech Dev. 1998 Jul;75(1-2):107-15. doi: 10.1016/s0925-4773(98)00090-2.
A basic limitation of the study of development in the mouse is the inaccessibility of the embryos, which are encased in the maternal uterus. We demonstrate the first use of ultrasound backscatter microscopy for guiding injections of cells and other agents into early stage mouse embryos. Cells were injected into the mouse neural tube cavity as early as 9.5 days post coitus (E9.5), and into the developing limb buds as early as E10.5. Furthermore, a cell-line engineered to express the secreted factor Sonic Hedgehog (Shh) was injected into early developing mouse brains or limbs. The Shh-expressing cells were found to induce ectopic expression of the Shh target genes Patched and Hnf3beta in the dorsal brain, and to alter digit patterning in the anterior limb bud. These results show that gene misexpression studies can be performed in mouse embryos using ultrasound-guided injection of transfected cells or retroviruses. In combination with the many available mouse mutants, this method offers a new approach for analyzing genetic interactions through gain-of-function studies performed in mutant mouse backgrounds.
对小鼠发育进行研究的一个基本限制是胚胎难以获取,因为它们位于母体子宫内。我们首次展示了利用超声背散射显微镜引导将细胞和其他试剂注入早期小鼠胚胎。早在交配后9.5天(E9.5)就将细胞注入小鼠神经管腔,早在E10.5就将细胞注入发育中的肢芽。此外,将经过基因工程改造以表达分泌因子音猬因子(Shh)的细胞系注入早期发育的小鼠脑或肢体。发现表达Shh的细胞可诱导Shh靶基因Patched和Hnf3β在背脑异位表达,并改变前肢芽中的指型模式。这些结果表明,利用超声引导注射转染细胞或逆转录病毒,可以在小鼠胚胎中进行基因错误表达研究。结合许多现有的小鼠突变体,这种方法为通过在突变小鼠背景中进行功能获得性研究来分析基因相互作用提供了一种新方法。