Abstract

Mammalian embryonic development starts with a single fertilized zygote that develops into a blastocyst embryo consisting of three cell types that evolve into either embryonic or extra-embryonic tissues. Lineage tracing of these cells can provide important information about the molecular and cellular dynamics contributing to fate allocation during early development. While global labeling techniques allow for visualization of all cells at the same time, lineage tracing of cells over several divisions can become complicated due to embryo movement and rotation as well as increasing cell densities. Here, we use green-to-red photoconvertible proteins for both global and sparse labeling of cells of interest in the developing murine embryo. We use primed conversion to achieve precise photoconversion of single nuclei in 4-cell stage embryos followed by volumetric live imaging to capture development up to the blastocyst stage. We developed an image analysis pipeline, called primed Track, that uses the dual labeling strategy for both straightforward segmentation and registration of all cells in the embryo as well as correction of rotational and spatial drift. Together, this strategy allows for reliable and fast tracking and lineage tracing of individual cells, even over increased imaging time intervals that result in a major reduction in data volume, all essential conditions for volumetric long-term imaging techniques.

Highlights

  • This page was generated automatically upon download from the ETH Zurich Research Collection

  • Lineage tracing of these cells can provide important information about the molecular and cellular dynamics contributing to fate allocation during early development

  • While global labeling techniques allow for visualization of all cells at the same time, lineage tracing of cells over several divisions can become complicated due to embryo movement and rotation as well as increasing cell densities

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Summary

Procedure

3. Prepare a sample holder for the LS1 light-sheet microscope with ~10-15 μl KSOM covered with ~300 μl mineral oil and leave it in a CO2 incubator until use. Right after performing confined primed conversion on single nuclei of mouse embryos, transfer 10-15 embryos to a pre-equilibrated sample holder for the LS1 light-sheet microscope system (Step A3). Step-by-step segmentation, tracking and lineage tracing using primed Track The acquired time-lapse 3D images of photoconverted mouse embryos in two channels can be analyzed using primed Track, in which a custom MATLAB code is used and implemented in Imaris (Bitplane). 5. Low green fluorescent signal can lead to failure of detection for segmentation and false deletion of red spots in the previous step. To compensate for this, the user has to option to recover these red spots if a valid red spot was present at the previous time point within a user-defined search radius

Three new spot objects will be created
Re-align embryo with the next function in the Imaris menu

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