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Utilizing convolutional neural networks for discriminating cancer and stromal cells in three-dimensional cell culture images with nuclei counterstain.
Nguyen, Huu Tuan; Pietraszek, Nicholas; Shelton, Sarah E; Arthur, Kwabena; Kamm, Roger D.
Afiliação
  • Nguyen HT; Massachusetts Institute of Technology (MIT), Department of Mechanical Engineering and Department of Biological Engineering, Cambridge, Massachusetts, United States.
  • Pietraszek N; Massachusetts Institute of Technology (MIT), Department of Mechanical Engineering and Department of Biological Engineering, Cambridge, Massachusetts, United States.
  • Shelton SE; Massachusetts Institute of Technology (MIT), Department of Mechanical Engineering and Department of Biological Engineering, Cambridge, Massachusetts, United States.
  • Arthur K; Massachusetts Institute of Technology (MIT), Department of Mechanical Engineering and Department of Biological Engineering, Cambridge, Massachusetts, United States.
  • Kamm RD; Massachusetts Institute of Technology (MIT), Department of Mechanical Engineering and Department of Biological Engineering, Cambridge, Massachusetts, United States.
J Biomed Opt ; 29(Suppl 2): S22710, 2024 Jun.
Article em En | MEDLINE | ID: mdl-39184400
ABSTRACT

Significance:

Accurate cell segmentation and classification in three-dimensional (3D) images are vital for studying live cell behavior and drug responses in 3D tissue culture. Evaluating diverse cell populations in 3D cell culture over time necessitates non-toxic staining methods, as specific fluorescent tags may not be suitable, and immunofluorescence staining can be cytotoxic for prolonged live cell cultures.

Aim:

We aim to perform machine learning-based cell classification within a live heterogeneous cell culture population grown in a 3D tissue culture relying only on reflectance, transmittance, and nuclei counterstained images obtained by confocal microscopy.

Approach:

In this study, we employed a supervised convolutional neural network (CNN) to classify tumor cells and fibroblasts within 3D-grown spheroids. These cells are first segmented using the marker-controlled watershed image processing method. Training data included nuclei counterstaining, reflectance, and transmitted light images, with stained fibroblast and tumor cells as ground-truth labels.

Results:

Our results demonstrate the successful marker-controlled watershed segmentation of 84% of spheroid cells into single cells. We achieved a median accuracy of 67% (95% confidence interval of the median is 65-71%) in identifying cell types. We also recapitulate the original 3D images using the CNN-classified cells to visualize the original 3D-stained image's cell distribution.

Conclusion:

This study introduces a non-invasive toxicity-free approach to 3D cell culture evaluation, combining machine learning with confocal microscopy, opening avenues for advanced cell studies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Núcleo Celular / Redes Neurais de Computação / Células Estromais Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Núcleo Celular / Redes Neurais de Computação / Células Estromais Idioma: En Ano de publicação: 2024 Tipo de documento: Article