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Predicting gene expression using morphological cell responses to nanotopography

Author

Listed:
  • Marie F. A. Cutiongco

    (University of Glasgow)

  • Bjørn Sand Jensen

    (University of Glasgow)

  • Paul M. Reynolds

    (University of Glasgow)

  • Nikolaj Gadegaard

    (University of Glasgow)

Abstract

Cells respond in complex ways to their environment, making it challenging to predict a direct relationship between the two. A key problem is the lack of informative representations of parameters that translate directly into biological function. Here we present a platform to relate the effects of cell morphology to gene expression induced by nanotopography. This platform utilizes the ‘morphome’, a multivariate dataset of cell morphology parameters. We create a Bayesian linear regression model that uses the morphome to robustly predict changes in bone, cartilage, muscle and fibrous gene expression induced by nanotopography. Furthermore, through this model we effectively predict nanotopography-induced gene expression from a complex co-culture microenvironment. The information from the morphome uncovers previously unknown effects of nanotopography on altering cell–cell interaction and osteogenic gene expression at the single cell level. The predictive relationship between morphology and gene expression arising from cell-material interaction shows promise for exploration of new topographies.

Suggested Citation

  • Marie F. A. Cutiongco & Bjørn Sand Jensen & Paul M. Reynolds & Nikolaj Gadegaard, 2020. "Predicting gene expression using morphological cell responses to nanotopography," Nature Communications, Nature, vol. 11(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-15114-1
    DOI: 10.1038/s41467-020-15114-1
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    Cited by:

    1. Duy Pham & Xiao Tan & Brad Balderson & Jun Xu & Laura F. Grice & Sohye Yoon & Emily F. Willis & Minh Tran & Pui Yeng Lam & Arti Raghubar & Priyakshi Kalita-de Croft & Sunil Lakhani & Jana Vukovic & Ma, 2023. "Robust mapping of spatiotemporal trajectories and cell–cell interactions in healthy and diseased tissues," Nature Communications, Nature, vol. 14(1), pages 1-25, December.
    2. Greta Simionato & Konrad Hinkelmann & Revaz Chachanidze & Paola Bianchi & Elisa Fermo & Richard van Wijk & Marc Leonetti & Christian Wagner & Lars Kaestner & Stephan Quint, 2021. "Red blood cell phenotyping from 3D confocal images using artificial neural networks," PLOS Computational Biology, Public Library of Science, vol. 17(5), pages 1-17, May.
    3. Lisa Laux & Marie F A Cutiongco & Nikolaj Gadegaard & Bjørn Sand Jensen, 2020. "Interactive machine learning for fast and robust cell profiling," PLOS ONE, Public Library of Science, vol. 15(9), pages 1-16, September.
    4. John Arevalo & Ellen Su & Jessica D. Ewald & Robert Dijk & Anne E. Carpenter & Shantanu Singh, 2024. "Evaluating batch correction methods for image-based cell profiling," Nature Communications, Nature, vol. 15(1), pages 1-12, December.

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