| Autor: |
John W. Wills, Jack Robertson, Pani Tourlomousis, Clare M.C. Gillis, Claire M. Barnes, Michelle Miniter, Rachel E. Hewitt, Clare E. Bryant, Huw D. Summers, Jonathan J. Powell, Paul Rees |
| Jazyk: |
angličtina |
| Rok vydání: |
2023 |
| Předmět: |
|
| Zdroj: |
Cell Reports: Methods, Vol 3, Iss 2, Pp 100398- (2023) |
| Druh dokumentu: |
article |
| ISSN: |
2667-2375 |
| DOI: |
10.1016/j.crmeth.2023.100398 |
| Popis: |
Summary: Unlocking and quantifying fundamental biological processes through tissue microscopy requires accurate, in situ segmentation of all cells imaged. Currently, achieving this is complex and requires exogenous fluorescent labels that occupy significant spectral bandwidth, increasing the duration and complexity of imaging experiments while limiting the number of channels remaining to address the study’s objectives. We demonstrate that the excitation light reflected during routine confocal microscopy contains sufficient information to achieve accurate, label-free cell segmentation in 2D and 3D. This is achieved using a simple convolutional neural network trained to predict the probability that reflected light pixels belong to either nucleus, cytoskeleton, or background classifications. We demonstrate the approach across diverse lymphoid tissues and provide video tutorials demonstrating deployment in Python and MATLAB or via standalone software for Windows. Motivation: Across the biomedical sciences, there is an urgent need to move beyond qualitative imaging to quantitative, cell-based reporting of tissue microscopy data. Typically, cell segmentation requires fluorescent labeling of nucleus and cytoplasm, which limits the spectral bandwidth available for other reporter molecules. However, recent advances in deep-learning algorithms have transformed automated image classification, and this raises the possibility of proceeding with reduced image information. Here, we show that 2D and 3D cell segmentation of lymphoid tissues can be freely established from the reflected laser excitation light always present during routine confocal microscopy using entirely standard equipment. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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