Wang Qiang, Akram Ahsan R, Dorward David A, Talas Sophie, Monks Basil, Thum Chee, Hopgood James R, Javidi Malihe, Vallejo Marta
Centre for Inflammation Research, Institute of Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.
Translational Healthcare Technologies Group, Centre for Inflammation Research, Institute of Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.
Npj Imaging. 2024;2(1):17. doi: 10.1038/s44303-024-00021-7. Epub 2024 Jun 28.
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.
无标记自发荧光寿命是生物样本中天然荧光团发出的固有荧光信号的独特特征。荧光寿命成像显微镜(FLIM)可以捕获这些信号,从而对生物样本进行全面分析。尽管FLIM在生物医学和临床科学中具有根本重要性和广泛应用,但现有的FLIM图像分析方法在没有可靠参考(如组织学图像)的情况下,往往难以提供快速准确的解读,而组织学图像通常不会与FLIM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)的方法来生成虚拟苏木精和伊红(H&E)染色。通过将先进的DL模型与当代图像质量指标相结合,我们可以从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,纳入寿命信息(强度之外的额外维度)会导致虚拟染色的重建更准确。这一进展使得在细胞水平上能够即时准确地解读FLIM图像,而无需处理FLIM图像与组织学图像配准的复杂性。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独特寿命特征,为跨多种癌症类型使用FLIM进行无生物标志物组织学研究开辟新机遇。