A Bayesian framework for inferring dynamic intercellular interactions from time-series single-cell data

Characterizing cell-cell communication and tracking its variability over time are crucial for understanding the coordination of biological processes mediating normal development, disease progression, and responses to perturbations such as therapies. Existing tools fail to capture time-dependent intercellular interactions and primarily rely on databases compiled from limited contexts. We introduce DIISCO, a Bayesian framework designed to characterize the temporal dynamics of cellular interactions using single-cell RNA-sequencing data from multiple time points. Our method utilizes structured Gaussian process regression to unveil time-resolved interactions among diverse cell types according to their coevolution and incorporates prior knowledge of receptor-ligand complexes. We show the interpretability of DIISCO in simulated data and new data collected from T cells cocultured with lymphoma cells, demonstrating its potential to uncover dynamic cell-cell cross talk.

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Publication Details

Journal
Genome Research
Published
2024-09-01
DOI
https://doi.org/10.1101/gr.279126.124
Citations
9
Primary Topic
Single-cell and spatial transcriptomics
Type
article

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article

A Bayesian framework for inferring dynamic intercellular interactions from time-series single-cell data

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Genome Research
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article

A Bayesian framework for inferring dynamic intercellular interactions from time-series single-cell data

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article en
9 citations

Abstract

Characterizing cell-cell communication and tracking its variability over time are crucial for understanding the coordination of biological processes mediating normal development, disease progression, and responses to perturbations such as therapies. Existing tools fail to capture time-dependent intercellular interactions and primarily rely on databases compiled from limited contexts. We introduce DIISCO, a Bayesian framework designed to characterize the temporal dynamics of cellular interactions using single-cell RNA-sequencing data from multiple time points. Our method utilizes structured Gaussian process regression to unveil time-resolved interactions among diverse cell types according to their coevolution and incorporates prior knowledge of receptor-ligand complexes. We show the interpretability of DIISCO in simulated data and new data collected from T cells cocultured with lymphoma cells, demonstrating its potential to uncover dynamic cell-cell cross talk.

Genome ResearchVol. 34(9)
Broad Institute (US), Harvard University (US), Dana-Farber Cancer Institute (US), New York Genome Center (US), Columbia University (US)
Leukemia and Lymphoma Society, Columbia University, New York Genome Center, National Institutes of Health, National Cancer Institute
Single-cell and spatial transcriptomics
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