基于PCNA的HeLa细胞S相亚相和RFC依赖动力学的轻量级CNN识别。

IF 1.9 4区 医学 Q4 NEUROSCIENCES
Maciej Krupa, Jędrzej Szymański
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引用次数: 0

摘要

增殖细胞核抗原(PCNA)形成亚核复制模式,用单个标记报告S期进展,并提供复制因子C (RFC) - PCNA轴的成像读数。我们对轻量级卷积神经网络进行基准测试,将固定的HeLa细胞PCNA图像分类为G1、S早期、S中期或S晚期,然后将表现最佳的模型应用于活细胞RFC控制和RFC - del数据集。MobileNetV2在固定单元基准测试中提供了精度和推理成本的最佳平衡。在活细胞痕迹中,RFC模型细胞显示出延长的晚期S样PCNA模式持续时间,而中期S样持续时间和峰距指标没有显示出明显的组分离。这些发现支持轻量级PCNA模式分类作为定量复制模式表型的实用工具,并表明未来可能应用于神经生物学成像,如神经发生研究中增殖细胞的自动定量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lightweight CNN recognition of HeLa cell PCNA‑based S‑phase subphases and RFC‑dependent dynamics.

Proliferating cell nuclear antigen (PCNA) forms subnuclear replication patterns that report S‑phase progression with a single marker and provide an imaging readout of the replication factor C (RFC)‑PCNA axis. We benchmarked lightweight convolutional neural networks for classifying fixed HeLa cell PCNA images as G1, early S, mid S, or late S, and then applied the best‑performing model to live‑cell RFC control and RFC‑del datasets. MobileNetV2 provided the best balance of accuracy and inference cost in the fixed‑cell benchmark. In live‑cell traces, RFC‑del cells showed prolonged late S‑like PCNA pattern duration, whereas mid S‑like duration and peak‑distance metrics did not show clear group separation. These findings support lightweight PCNA‑pattern classification as a practical tool for quantitative replication‑pattern phenotyping and indicate a possible future application to neurobiological imaging, such as automated quantification of pro liferating cells in neurogenesis studies.

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来源期刊
CiteScore
2.20
自引率
7.10%
发文量
40
审稿时长
>12 weeks
期刊介绍: Acta Neurobiologiae Experimentalis (ISSN: 0065-1400 (print), eISSN: 1689-0035) covers all aspects of neuroscience, from molecular and cellular neurobiology of the nervous system, through cellular and systems electrophysiology, brain imaging, functional and comparative neuroanatomy, development and evolution of the nervous system, behavior and neuropsychology to brain aging and pathology, including neuroinformatics and modeling.
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