Classification of T lymphocyte motility behaviors using a machine learning approach.

IF 4.3 2区 生物学
PLoS Computational Biology Pub Date : 2023-09-11 eCollection Date: 2023-09-01 DOI:10.1371/journal.pcbi.1011449
Yves Carpentier Solorio, Florent Lemaître, Bassam Jabbour, Olivier Tastet, Nathalie Arbour, Elie Bou Assi
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引用次数: 0

Abstract

T lymphocytes migrate into organs and interact with local cells to perform their functions. How human T lymphocytes communicate with organ-specific cells and participate in pathobiological processes remains unresolved. Brain infiltration of T lymphocytes is associated with multiple neurological disorders. Thus, to characterize the behavior of human T lymphocytes reaching the human brain, we performed time-lapse microscopy on human CD8+ T lymphocytes co-cultured with either primary human astrocytes or neurons. Using traditional manual and visual assessment of microscopy data, we identified distinct CD8+ T lymphocyte motility behaviors. However, such characterization is time and labor-intensive. In this work, we trained and validated a machine-learning model for the automated classification of behaviors of CD8+ T lymphocytes interacting with astrocytes and neurons. A balanced random forest was trained for the binary classification of established classes of cell behaviors (synapse vs. kinapse) as well as visually identified behaviors (scanning, dancing, and poking). Feature selection was performed during 3-fold cross-validation using the minimum redundancy maximum relevance algorithm. Results show promising performances when tested on a held-out dataset of CD8+ T lymphocytes interacting with astrocytes with a new experimenter and a held-out independent dataset of CD8+ T lymphocytes interacting with neurons. When tested on the independent CD8+ T cell-neuron dataset, the final model achieved a binary classification accuracy of 0.82 and a 3-class accuracy of 0.79. This novel automated classification approach could significantly reduce the time required to label cell motility behaviors while facilitating the identification of interactions of T lymphocytes with multiple cell types.

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使用机器学习方法对T淋巴细胞运动行为进行分类。
T淋巴细胞迁移到器官中,并与局部细胞相互作用以发挥其功能。人类T淋巴细胞如何与器官特异性细胞通讯并参与病理生物学过程尚未解决。脑内T淋巴细胞浸润与多种神经系统疾病有关。因此,为了表征人类T淋巴细胞到达人脑的行为,我们对与原代人类星形胶质细胞或神经元共培养的人类CD8+T淋巴细胞进行了延时显微镜检查。使用显微镜数据的传统手动和视觉评估,我们确定了不同的CD8+T淋巴细胞运动行为。然而,这样的定性需要时间和劳动密集型。在这项工作中,我们训练并验证了一个机器学习模型,用于CD8+T淋巴细胞与星形胶质细胞和神经元相互作用行为的自动分类。训练了一个平衡的随机森林,用于对已建立的细胞行为类别(突触与突触)以及视觉识别的行为(扫描、跳舞和戳)进行二元分类。在使用最小冗余-最大相关性算法的三次交叉验证期间进行特征选择。当用新的实验者在CD8+T淋巴细胞与星形胶质细胞相互作用的固定数据集和CD8+T细胞与神经元相互作用的独立数据集上测试时,结果显示出有希望的性能。当在独立的CD8+T细胞神经元数据集上测试时,最终模型实现了0.82的二元分类准确度和0.79的三类准确度。这种新的自动分类方法可以显著减少标记细胞运动行为所需的时间,同时有助于识别T淋巴细胞与多种细胞类型的相互作用。
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来源期刊
PLoS Computational Biology
PLoS Computational Biology 生物-生化研究方法
CiteScore
7.10
自引率
4.70%
发文量
820
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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