4.7 Article

4D atlas of the mouse embryo for precise morphological staging

Journal

DEVELOPMENT
Volume 142, Issue 20, Pages 3583-3591

Publisher

COMPANY OF BIOLOGISTS LTD
DOI: 10.1242/dev.125872

Keywords

OPT; Embryo; 3D; 4D; Imaging; Development; Staging

Funding

  1. Genome Canada
  2. Natural Sciences and Engineering Research Council of Canada [402148]
  3. Canada Research Chair award
  4. Canada Research Chair in Imaging Technologies in Human Diseases and Preclinical Models

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After more than a century of research, the mouse remains the gold-standard model system, for it recapitulates human development and disease and is quickly and highly tractable to genetic manipulations. Fundamental to the power and success of using a mouse model is the ability to stage embryonic mouse development accurately. Past staging systems were limited by the technologies of the day, such that only surface features, visible with a light microscope, could be recognized and used to define stages. With the advent of high-throughput 3D imaging tools that capture embryo morphology in microscopic detail, we now present the first 4D atlas staging system for mouse embryonic development using optical projection tomography and image registration methods. By tracking 3D trajectories of every anatomical point in the mouse embryo from E11.5 to E14.0, we established the first 4D atlas compiled from ex vivo 3D mouse embryo reference images. The resulting 4D atlas comprises 51 interpolated 3D images in this gestational range, resulting in a temporal resolution of 72 min. From this 4D atlas, any mouse embryo image can be subsequently compared and staged at the global, voxel and/or structural level. Assigning an embryonic stage to each point in anatomy allows for unprecedented quantitative analysis of developmental asynchrony among different anatomical structures in the same mouse embryo. This comprehensive developmental data set offers developmental biologists a new, powerful staging system that can identify and compare differences in developmental timing in wild-type embryos and shows promise for localizing deviations in mutant development.

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