Label-free evaluation of mouse embryo quality using time-lapse bright field and optical coherence microscopy

The selection of high-quality embryos is essential to enhance the implantation rate for in vitro fertilization (IVF). Optical coherence microscopy (OCM) can noninvasively provide three-dimensional (3D) high-resolution imaging of developing embryos. The revealed microstructures can be used for accurate embryo evaluation. Here, we acquire time-lapse 3D OCM images with co-registered bright-field imaging on mouse embryo development from the one-cell stage to the fully hatched blastocyst inside an incubator. Our results demonstrate the capability of OCM to detect structural features of the developing embryos. The second and third embryonic cell cycles are indicated to be associated with blastocyst formation and the hatching capability. OCM-based time-lapse technology holds the potential to enrich early embryo development insights and streamline embryo selection within IVF clinics.

Authors

Institutions

Publication Details

Journal
Communications Biology
Published
2025-04-15
DOI
https://doi.org/10.1038/s42003-025-08044-5
Citations
4
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
6.54

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Label-free evaluation of mouse embryo quality using time-lapse bright field and optical coherence microscopy

Fei Wang, Chao Zhou, Senyue Hao, Kibeom Park et al.
4 citations
Communications Biology
Advanced Fluorescence Microscopy Techniques
6.54
article

Label-free evaluation of mouse embryo quality using time-lapse bright field and optical coherence microscopy

Fei Wang, Chao Zhou, Senyue Hao, Kibeom Park, Ali Ahmady
article en
4 citations

Abstract

The selection of high-quality embryos is essential to enhance the implantation rate for in vitro fertilization (IVF). Optical coherence microscopy (OCM) can noninvasively provide three-dimensional (3D) high-resolution imaging of developing embryos. The revealed microstructures can be used for accurate embryo evaluation. Here, we acquire time-lapse 3D OCM images with co-registered bright-field imaging on mouse embryo development from the one-cell stage to the fully hatched blastocyst inside an incubator. Our results demonstrate the capability of OCM to detect structural features of the developing embryos. The second and third embryonic cell cycles are indicated to be associated with blastocyst formation and the hatching capability. OCM-based time-lapse technology holds the potential to enrich early embryo development insights and streamline embryo selection within IVF clinics.

Communications BiologyVol. 8(1)
Washington University in St. Louis (US)
American Society for Reproductive Medicine, Washington University in St. Louis
Openalex Percentile: Top 4%
Advanced Fluorescence Microscopy Techniques
6.54
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.