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超声背散射显微镜引导的脑室基因传递在小鼠胚胎龄 9.5 和 10.5 时产生了明显不同的成年期转基因表达模式。

Ultrasound backscatter microscopy image-guided intraventricular gene delivery at murine embryonic age 9.5 and 10.5 produces distinct transgene expression patterns at the adult stage.

出版信息

Mol Imaging. 2013 Nov-Dec;12(8). doi: 10.2310/7290.2013.00067.

DOI:10.2310/7290.2013.00067
PMID:24447614
Abstract

In utero injection of a retroviral vector into the embryonic telencephalon aided by ultrasound backscatter microscopy permits introduction of a gene of interest at an early stage of development. In this study, we compared the tissue distribution of gene expression in adult mice injected with retroviral vectors at different embryonic ages in utero. Following ultrasound image-guided gene delivery (UIGD) into the embryonic telencephalon, adult mice were subjected to whole-body luciferase imaging and immunohistochemical analysis at 6 weeks and 1 year postinjection. Luciferase activity was observed in a wide range of tissues in animals injected at embryonic age 9.5 (E9.5), whereas animals injected at E10.5 showed brain-localized reporter gene expression. These results suggest that mouse embryonic brain creates a closed and impermeable structure around E10. Therefore, by injecting a transgene before or after E10, transgene expression can be manipulated to be local or systemic. Our results also provide information that widens the applicability of UIGD beyond neuroscience studies.

摘要

在胚胎端脑内通过超声背向散射显微镜辅助注入逆转录病毒载体,可在发育早期将目的基因导入。在这项研究中,我们比较了在不同胚胎期经子宫内注射逆转录病毒载体的成年小鼠的组织分布。在胚胎端脑进行超声引导基因传递(UIGD)后,在注射后 6 周和 1 年内对成年小鼠进行全身荧光素酶成像和免疫组织化学分析。在 E9.5 时注射的动物中观察到了广泛的组织中的荧光素酶活性,而在 E10.5 时注射的动物则显示出脑内定位的报告基因表达。这些结果表明,小鼠胚胎大脑在 E10 左右形成一个封闭且不可渗透的结构。因此,通过在 E10 之前或之后注射转基因,可以操纵转基因表达使其成为局部或全身性的。我们的结果还提供了信息,扩大了 UIGD 在神经科学研究以外的适用性。

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Ultrasound backscatter microscopy image-guided intraventricular gene delivery at murine embryonic age 9.5 and 10.5 produces distinct transgene expression patterns at the adult stage.超声背散射显微镜引导的脑室基因传递在小鼠胚胎龄 9.5 和 10.5 时产生了明显不同的成年期转基因表达模式。
Mol Imaging. 2013 Nov-Dec;12(8). doi: 10.2310/7290.2013.00067.
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