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Three-dimensional microCT imaging of murine embryonic development from immediate post-implantation to organogenesis: application for phenotyping analysis of early embryonic lethality in mutant animals

机译:从立即植入后到器官发生的小鼠胚胎发育的三维microCT成像:在突变动物的早期胚胎致死性表型分析中的应用

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摘要

In this work, we applied three-dimensional microCT imaging to study murine embryogenesis in the range from immediate post-implantation period (embryonic day 5.5) to mid-gestation (embryonic day 12.5) with the resolution up to 1.4 µm/voxel. Also, we introduce an imaging procedure for non-invasive volumetric estimation of an entire litter of embryos within the maternal uterine structures. This method allows for an accurate, detailed and systematic morphometric analysis of both embryonic and extra-embryonic components during embryogenesis. Three-dimensional imaging of unperturbed embryos was performed to visualize the egg cylinder, primitive streak, gastrulation and early organogenesis stages of murine development in the C57Bl6/N mouse reference strain. Further, we applied our microCT imaging protocol to determine the earliest point when embryonic development is arrested in a mouse line with knockout for tRNA splicing endonuclease subunit Tsen54 gene. Our analysis determined that the embryonic development in Tsen54 null embryos does not proceed beyond implantation. We demonstrated that application of microCT imaging to entire litter of non-perturbed embryos greatly facilitate studies to unravel gene function during early embryogenesis and to determine the precise point at which embryonic development is arrested in mutant animals. The described method is inexpensive, does not require lengthy embryos dissection and can be applicable for detailed analysis of mutant mice at laboratory scale as well as for high-throughput projects.Electronic supplementary materialThe online version of this article (doi:10.1007/s00335-017-9723-6) contains supplementary material, which is available to authorized users.
机译:在这项工作中,我们应用了三维microCT成像技术来研究从植入后立即(胚胎第5.5天)到妊娠中期(胚胎第12.5天)的小鼠胚胎发生,分辨率高达1.4μm/体素。此外,我们介绍了一种成像程序,用于对母体子宫结构内的整个胚胎胚胎进行非侵入式体积估计。这种方法可以在胚胎发生过程中对胚胎和胚外成分进行准确,详细和系统的形态分析。在C57B16 / N小鼠参考菌株中对未受扰动的胚胎进行了三维成像,以可视化卵瓶,原始条纹,胃形成和小鼠发育的早期器官发生阶段。此外,我们应用了microCT成像协议来确定最早的胚胎发育停滞在敲除tRNA剪接核酸内切酶Tsen54基因的tRNA的小鼠品系中的时间。我们的分析确定,Tsen54空胚的胚胎发育不会超出植入过程。我们证明了将microCT成像应用于未受扰动的胚胎的整个产仔极大地促进了研究在早期胚胎发生过程中揭示基因功能,并确定了在突变动物中逮捕胚胎发育的精确点。所描述的方法价格便宜,不需要冗长的胚胎解剖,可用于实验室规模的突变小鼠的详细分析以及高通量项目。电子补充材料本文的在线版本(doi:10.1007 / s00335-017) -9723-6)包含补充材料,授权用户可以使用。

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