Peavey Mary C, Reynolds Corey L, Szwarc Maria M, Gibbons William E, Valdes Cecilia T, DeMayo Francesco J, Lydon John P
Devision of Repreoductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, Baylor College of Medicine; Department of Molecular and Cellular Biology, Baylor College of Medicine.
Mouse Phenotyping Core, Baylor College of Medicine.
J Vis Exp. 2017 Oct 24(128):56207. doi: 10.3791/56207.
High-frequency ultrasonography (HFUS) is a common method to non-invasively monitor the real-time development of the human fetus in utero. The mouse is routinely used as an in vivo model to study embryo implantation and pregnancy progression. Unfortunately, such murine studies require pregnancy interruption to enable follow-up phenotypic analysis. To address this issue, we used three-dimensional (3-D) reconstruction of HFUS imaging data for early detection and characterization of murine embryo implantation sites and their individual developmental progression in utero. Combining HFUS imaging with 3-D reconstruction and modeling, we were able to accurately quantify embryo implantation site number as well as monitor developmental progression in pregnant C57BL6J/129S mice from 5.5 days post coitus (d.p.c.) through to 9.5 d.p.c. with the use of a transducer. Measurements included: number, location, and volume of implantation sites as well as inter-implantation site spacing; embryo viability was assessed by cardiac activity monitoring. In the immediate post-implantation period (5.5 to 8.5 d.p.c.), 3-D reconstruction of the gravid uterus in both mesh and solid overlay format enabled visual representation of the developing pregnancies within each uterine horn. As genetically engineered mice continue to be used to characterize female reproductive phenotypes derived from uterine dysfunction, this method offers a new approach to detect, quantify, and characterize early implantation events in vivo. This novel use of 3-D HFUS imaging demonstrates the ability to successfully detect, visualize, and characterize embryo-implantation sites during early murine pregnancy in a non-invasive manner. The technology offers a significant improvement over current methods, which rely on the interruption of pregnancies for gross tissue and histopathologic characterization. Here we use a video and text format to describe how to successfully perform ultrasounds of early murine pregnancy to generate reliable and reproducible data with reconstruction of the uterine form in mesh and solid 3-D images.
高频超声检查(HFUS)是一种非侵入性监测子宫内人类胎儿实时发育情况的常用方法。小鼠通常被用作体内模型来研究胚胎着床和妊娠进展。不幸的是,此类小鼠研究需要中断妊娠以便进行后续的表型分析。为解决这一问题,我们利用HFUS成像数据的三维(3-D)重建来早期检测和表征小鼠胚胎着床部位及其在子宫内的个体发育进程。将HFUS成像与3-D重建及建模相结合,我们能够通过使用换能器准确量化妊娠C57BL6J/129S小鼠从交配后5.5天(d.p.c.)至9.5 d.p.c.期间的胚胎着床部位数量,并监测其发育进程。测量内容包括:着床部位的数量、位置和体积以及着床部位之间的间距;通过监测心脏活动评估胚胎活力。在着床后即刻阶段(5.5至8.5 d.p.c.),以网格和实体叠加形式对妊娠子宫进行3-D重建,能够直观呈现每个子宫角内发育中的妊娠情况。随着基因工程小鼠继续被用于表征源自子宫功能障碍的雌性生殖表型,该方法为体内检测、量化和表征早期着床事件提供了一种新途径。这种3-D HFUS成像的新应用证明了能够以非侵入性方式成功检测、可视化并表征小鼠早期妊娠期间的胚胎着床部位。该技术相较于目前依赖中断妊娠进行大体组织和组织病理学表征的方法有显著改进。在此我们采用视频和文本形式描述如何成功进行小鼠早期妊娠的超声检查,以通过子宫形态的网格和实体3-D图像重建生成可靠且可重复的数据。