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Related Concept Videos

Cleavage and Blastulation01:33

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After a large-single-celled zygote is produced via fertilization, the process of cleavage occurs while zygotes travel through the uterine tube. Cleavage is a mitotic cell division that does not result in growth. With each round of successive cell division, daughter cells get increasingly smaller.
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Morphometric Protocol for the Objective Assessment of Blastocyst Behavior During Vitrification and Warming Steps
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3D Morphology Measurement for Blastocyst Evaluation From "All Angles".

Guanqiao Shan, Changsheng Dai, Hang Liu

    IEEE Transactions on Bio-Medical Engineering
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    Summary

    This study introduces a novel label-free method for 3D cell aggregate imaging. The technique accurately measures blastocyst morphology for improved in vitro fertilization (IVF) outcomes.

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    Area of Science:

    • Biomedical Engineering
    • Developmental Biology
    • Medical Imaging

    Background:

    • Accurate 3D morphology measurement of spherical cell aggregates is crucial for biological and medical applications.
    • Existing methods like fluorescent labeling induce toxicity and 2D estimations lack precision.
    • There is a need for non-invasive, quantitative 3D imaging techniques for clinical use.

    Purpose of the Study:

    • To develop and validate a quantitative, label-free 3D morphology measurement technique for spherical cell aggregates.
    • To enable comprehensive, multi-angle morphological evaluation of blastocysts for in vitro fertilization (IVF).
    • To overcome the limitations of current toxic and imprecise methods.

    Main Methods:

    • A multi-view imaging approach was employed for label-free 3D reconstruction.
    • Spherical Rotation Scale Invariant Feature Transform (SR-SIFT) was developed to handle feature distortions in multi-view images.
    • U-Net with generalized Dice loss was utilized for accurate segmentation of trophectoderm (TE) and inner cell mass (ICM).

    Main Results:

    • The developed technique achieved rotation angle errors below 1 degree.
    • High segmentation accuracy was demonstrated with Dice scores of 95.6% for TE and 92.3% for ICM.
    • Overall measurement error for clinically relevant blastocyst parameters was less than 6.7%.

    Conclusions:

    • The proposed label-free 3D morphology measurement technique offers a significant advancement over traditional methods.
    • This technique provides accurate and comprehensive morphological data for blastocysts, enhancing IVF applications.
    • The method's non-invasive nature and high precision make it suitable for clinical evaluation and research.