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将A/B细胞策略推导为用于延时显微镜的稳健多目标细胞流水线。

Deriving the A/B Cells Policy as a Robust Multi-Object Cell Pipeline for Time-Lapse Microscopy.

作者信息

Larin Ilya, Panferov Egor, Dodina Maria, Shaykhutdinova Diana, Larina Sofia, Minskaia Ekaterina, Karabelsky Alexander

机构信息

Translational Medicine Research Center, Sirius University of Science and Technology, Federal Territory Sirius, Olympic Ave. 1, 354340 Sirius, Russia.

IT-College, Sirius University of Science and Technology, Federal Territory Sirius, Olympic Ave. 1, 354340 Sirius, Russia.

出版信息

Int J Mol Sci. 2025 Aug 30;26(17):8455. doi: 10.3390/ijms26178455.

DOI:10.3390/ijms26178455
PMID:40943379
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12429040/
Abstract

Time-lapse microscopy of mesenchymal stem cell (MSC) cultures allows for the quantitative observation of their self-renewal, proliferation, and differentiation. However, the rigorous comparison of two conditions, baseline (A) versus perturbation (B) (the addition of molecular factors, environmental shifts, genetic modification, etc.), remains difficult because morphology, division timing, and migratory behavior are highly heterogeneous at the single-cell scale. MSCs can be used as an in vitro model to study cell morphology and kinetics in order to assess the effect of, for example, gene therapy and prime editing in the near future. By combining static, frame-wise morphology with dynamic descriptors, we can obtain weight profiles that highlight which morphological and behavioral dimensions drive divergence. In this study, we present A/B Cells Policy: a modular, open-source Python package implementing a robust cell tracking pipeline. It integrates a YOLO-based architecture as a two-stage assignment framework with fallback and recovery passes, re-identification of lost tracks, and lineage reconstruction. The framework links descriptive statistics to a transferable system, opening up avenues for regenerative medicine, pharmacology, and early translational pipelines. It does this by providing an interpretable, measurement-based bridge between in vitro imaging and in silico intervention strategy planning.

摘要

间充质干细胞(MSC)培养的延时显微镜技术能够对其自我更新、增殖和分化进行定量观察。然而,要严格比较两种条件,即基线(A)与扰动(B)(添加分子因子、环境变化、基因改造等),仍然很困难,因为在单细胞水平上,形态、分裂时间和迁移行为具有高度的异质性。间充质干细胞可作为体外模型来研究细胞形态和动力学,以便在不久的将来评估例如基因治疗和碱基编辑的效果。通过将静态的逐帧形态与动态描述符相结合,我们可以获得权重分布图,突出显示哪些形态和行为维度导致差异。在本研究中,我们提出了A/B细胞策略:一个模块化的开源Python包,实现了一个强大的细胞跟踪流程。它集成了基于YOLO的架构作为一个两阶段分配框架,包括备用和恢复过程、丢失轨迹的重新识别以及谱系重建。该框架将描述性统计与一个可转移系统相联系,为再生医学、药理学和早期转化流程开辟了道路。它通过在体外成像和计算机干预策略规划之间提供一个可解释的、基于测量的桥梁来实现这一点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab1/12429040/6cd12d658179/ijms-26-08455-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab1/12429040/f01ccf12bef3/ijms-26-08455-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab1/12429040/9de82ca27598/ijms-26-08455-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab1/12429040/34757193eb86/ijms-26-08455-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab1/12429040/6cd12d658179/ijms-26-08455-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab1/12429040/f01ccf12bef3/ijms-26-08455-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab1/12429040/e2a003235c44/ijms-26-08455-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab1/12429040/935388036e67/ijms-26-08455-g003.jpg
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Riemannian Manifolds for Biological Imaging Applications Based on Unsupervised Learning.基于无监督学习的生物成像应用黎曼流形
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Evaluating feature extraction in ovarian cancer cell line co-cultures using deep neural networks.
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Evaluation of mesenchymal stem cells as an model for inherited retinal diseases.间充质干细胞作为遗传性视网膜疾病模型的评估。
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