4.8 Article

Control of cell state transitions

Journal

NATURE
Volume 609, Issue 7929, Pages 975-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41586-022-05194-y

Keywords

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Funding

  1. NIH/NCI [R01CA244660]
  2. CRUK/Brain Tumour Charity grant [C42454/A28596]
  3. IRC grant [GOIPG/2020/1361]
  4. Science Foundation Ireland [14/IA/2395, 18/SPP/3522]
  5. Children's Health Foundation
  6. EU NanoCommons grant [731032]

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cSTAR is an approach for mapping cell states, modelling transitions between them, and predicting targeted interventions to convert cell fate decisions. It uses omics data as input, integrates signalling and phenotypic data, and provides new biological insights by simulating how cells manoeuvre in Waddington's landscape.
Understanding cell state transitions and purposefully controlling them is a longstanding challenge in biology. Here we present cell state transition assessment and regulation (cSTAR), an approach for mapping cell states, modelling transitions between them and predicting targeted interventions to convert cell fate decisions. cSTAR uses omics data as input, classifies cell states, and develops a work flow that transforms the input data into mechanistic models that identify a core signalling network, which controls cell fate transitions by influencing whole-cell networks. By integrating signalling and phenotypic data, cSTAR models how cells manoeuvre in Waddington's landscape' and make decisions about which cell fate to adopt. Notably, cSTAR devises interventions to control the movement of cells in Waddington's landscape. Testing cSTAR in a cellular model of differentiation and proliferation shows a high correlation between quantitative predictions and experimental data. Applying cSTARto different types of perturbation and omics datasets, including single-cell data, demonstrates its flexibility and scalability and provides new biological insights. The ability of cSTAR to identify targeted perturbations that interconvert cell fates will enable designer approaches for manipulating cellular development pathways and mechanistically underpinned therapeutic interventions.

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