基于深度学习的无标记自发荧光寿命图像虚拟 H&E 染色。

Qiang Wang, Ahsan R. Akram, David A. Dorward, Sophie Talas, Basil Monks, Chee Thum, James R. Hopgood, Malihe Javidi, Marta Vallejo
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引用次数: 0

摘要

无标记自发荧光寿命是生物样品中天然荧光团发出的固有荧光信号的一个独特特征。荧光寿命成像显微镜(FLIM)可以捕捉这些信号,从而对生物样本进行全面分析。尽管荧光寿命成像显微镜在生物医学和临床科学中具有根本性的重要意义和广泛应用,但现有的荧光寿命成像显微镜图像分析方法往往难以在没有可靠参照物(如组织学图像)的情况下提供快速、精确的解释,因为组织学图像通常无法与荧光寿命成像显微镜图像一起提供。为了解决这个问题,我们提出了一种基于深度学习(DL)的方法,用于生成虚拟的血红素和伊红(H&E)染色。通过将先进的深度学习模型与当代图像质量度量相结合,我们可以从在未染色组织样本上获取的无标记 FLIM 图像生成临床级虚拟 H&E 染色图像。我们的实验还表明,与仅使用强度图像相比,加入生命周期信息(强度之外的额外维度)能更准确地重建虚拟染色。这一进步使我们能够在细胞层面即时准确地解读 FLIM 图像,而无需处理 FLIM 和组织学图像的复杂性。因此,我们能够识别肿瘤微环境中常见的七种不同细胞类型的不同寿命特征,为在多种癌症类型中使用 FLIM 实现无生物标记组织组学开辟了新的机遇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Deep learning-based virtual H& E staining from label-free autofluorescence lifetime images
Label-free autofluorescence lifetime is a unique feature of the inherent fluorescence signals emitted by natural fluorophores in biological samples. Fluorescence lifetime imaging microscopy (FLIM) can capture these signals enabling comprehensive analyses of biological samples. Despite the fundamental importance and wide application of FLIM in biomedical and clinical sciences, existing methods for analysing FLIM images often struggle to provide rapid and precise interpretations without reliable references, such as histology images, which are usually unavailable alongside FLIM images. To address this issue, we propose a deep learning (DL)-based approach for generating virtual Hematoxylin and Eosin (H&E) staining. By combining an advanced DL model with a contemporary image quality metric, we can generate clinical-grade virtual H&E-stained images from label-free FLIM images acquired on unstained tissue samples. Our experiments also show that the inclusion of lifetime information, an extra dimension beyond intensity, results in more accurate reconstructions of virtual staining when compared to using intensity-only images. This advancement allows for the instant and accurate interpretation of FLIM images at the cellular level without the complexities associated with co-registering FLIM and histology images. Consequently, we are able to identify distinct lifetime signatures of seven different cell types commonly found in the tumour microenvironment, opening up new opportunities towards biomarker-free tissue histology using FLIM across multiple cancer types.
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