Webinar

Episode 2: Iodine-Contrast MicroCT Imaging for Mouse Embryo Development from Early Post-implantation to Early Postnatal Stages

BioXRM Lecture Series
19 January 2024 · 22 min watch
  • X-Ray Microscopy
  • Life Sciences
Profile Image of Doctor of Philosophy Chih-Wei Logan Hsu
Author Chih-Wei Logan Hsu, Ph.D. Assistant Professor, Co-Director of Optical Imaging and Vital Microscopy Core
Baylor College of Medicine
Episode 2 of 9

Abstract

Mouse models have long been a crucial tool for studying human disease, However, traditional methods of studying mouse embryos and phenotypes have been limited in their resolution and scope. The use of iodine contrast microCT has revolutionized our understanding of early development and embryonic abnormalities in mouse models. MicroCT imaging allows for non-destructive, 3D visualization of tissues and organs at high resolution, enabling researchers to study embryonic development and abnormalities with unprecedented detail.

As part of The International Mouse Phenotyping Consortium (IMPC), we have utilized iodine-contrast microCT to analyze mouse embryos and neonates from embryonic day 8.5 to postnatal day 3, while demonstrate that early-stage embryos can also be imaged without disturbance of extra embryonic tissues. This method allows for comprehensive analysis of embryo development, providing valuable insights into embryonic lethality in knockout mouse lines. Additionally, these techniques are cost-effective, easy to learn, and time- efficient, making them ideal for high-throughput analysis.

This presentation was recorded during the BioXRM symposium at the Museum of Natural History in London, October 2023.

Key Learnings:

  • Comprehensive analysis of embryo development can be achieved using X-ray microCT.
  • Established methods for sample preparation, including iodine contrast, make this approach ideal for high-throughput analysis.
  • The non-destructive assessment of iodine contrasted specimens has revolutionized current understanding of early development and embryonic abnormalities in mouse models.

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