Quantitative phase imaging with temporal kinetics predicts hematopoietic stem cell diversity

Innovative identification technologies for hematopoietic stem cells (HSCs) have expanded the scope of stem cell biology. Clinically, the functional quality of HSCs critically influences the safety and therapeutic efficacy of stem cell therapies. However, most analytical techniques capture only a single snapshot, disregarding the temporal context. A comprehensive understanding of the temporal heterogeneity of HSCs necessitates live-cell, real-time and non-invasive analysis. Here, we developed a prediction system for HSC diversity by integrating single-HSC ex vivo expansion technology with quantitative phase imaging (QPI)-driven machine learning. By analyzing the cellular kinetics of individual HSCs, we discovered previously undetectable diversity that snapshot analysis cannot resolve. The QPI-driven algorithm quantitatively evaluates stemness at the single-cell level and leverages temporal information to significantly improve prediction accuracy. This platform advances the field from snapshot-based identification of HSCs to dynamic, time-resolved prediction of their functional quality based on past cellular kinetics.

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Publication Details

Journal
Nature Communications
Published
2025-07-14
DOI
https://doi.org/10.1038/s41467-025-61846-3
Citations
1
Primary Topic
Digital Holography and Microscopy
Type
article
Field-Weighted Citation Impact
1.25

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Quantitative phase imaging with temporal kinetics predicts hematopoietic stem cell diversity

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Quantitative phase imaging with temporal kinetics predicts hematopoietic stem cell diversity

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article en
1 citations

Abstract

Innovative identification technologies for hematopoietic stem cells (HSCs) have expanded the scope of stem cell biology. Clinically, the functional quality of HSCs critically influences the safety and therapeutic efficacy of stem cell therapies. However, most analytical techniques capture only a single snapshot, disregarding the temporal context. A comprehensive understanding of the temporal heterogeneity of HSCs necessitates live-cell, real-time and non-invasive analysis. Here, we developed a prediction system for HSC diversity by integrating single-HSC ex vivo expansion technology with quantitative phase imaging (QPI)-driven machine learning. By analyzing the cellular kinetics of individual HSCs, we discovered previously undetectable diversity that snapshot analysis cannot resolve. The QPI-driven algorithm quantitatively evaluates stemness at the single-cell level and leverages temporal information to significantly improve prediction accuracy. This platform advances the field from snapshot-based identification of HSCs to dynamic, time-resolved prediction of their functional quality based on past cellular kinetics.

Nature CommunicationsVol. 16(1)
University of Tsukuba (JP), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Saitama International Medical Center (JP), Tokyo Women's Medical University (JP), Institute of Hematology & Blood Diseases Hospital (CN), The University of Tokyo (JP), Kumamoto University (JP)
Japan Agency for Medical Research and Development, Japan Society for the Promotion of Science, Institute of Medical Science, University of Tokyo
Zero hunger
Openalex Percentile: Top 19%
Digital Holography and Microscopy
1.25
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