Tracing cell communication programs across conditions at single cell resolution with CCC-RISE

Cell-cell communication (CCC) mediates coordinated cellular activities that vary dynamically across time, location, and biological context. While various tools exist to infer CCC, they typically aggregate data according to pre-defined cell types, obscuring critical single-cell heterogeneity. Furthermore, because signaling pathways and cell populations operate in a coordinated manner, an integrative analytical approach is essential. To address these challenges, we developed CCC-RISE, an extension of the tensor-based method Reduction and Insight in Single-cell Exploration (RISE). CCC-RISE identifies integrative patterns of single-cell variation by deconvolving communication into interpretable modules defined by unique sender cells, receiver cells, ligands, and condition associations. We applied this framework to a COVID-19 cohort with varying disease severity and a lung transplant cohort with acute allograft dysfunction. In both contexts, CCC-RISE successfully identified disease-relevant communication programs and traced them to specific cellular subpopulations, often crossing conventional cell-type boundaries. This approach offers a robust pipeline enabling the identification of disease-relevant signaling subpopulations that are invisible to aggregate methods.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-04-15
DOI
https://doi.org/10.64898/2026.04.14.718551
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
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article

Tracing cell communication programs across conditions at single cell resolution with CCC-RISE

Aaron S. Meyer, Andrew Ramirez, Nathaniel Thomas, John R Greenland et al.
bioRxiv (Cold Spring Harbor Laboratory)
Single-cell and spatial transcriptomics
article

Tracing cell communication programs across conditions at single cell resolution with CCC-RISE

Aaron S. Meyer, Andrew Ramirez, Nathaniel Thomas, John R Greenland, Daniel R Calabrese
article en

Abstract

Cell-cell communication (CCC) mediates coordinated cellular activities that vary dynamically across time, location, and biological context. While various tools exist to infer CCC, they typically aggregate data according to pre-defined cell types, obscuring critical single-cell heterogeneity. Furthermore, because signaling pathways and cell populations operate in a coordinated manner, an integrative analytical approach is essential. To address these challenges, we developed CCC-RISE, an extension of the tensor-based method Reduction and Insight in Single-cell Exploration (RISE). CCC-RISE identifies integrative patterns of single-cell variation by deconvolving communication into interpretable modules defined by unique sender cells, receiver cells, ligands, and condition associations. We applied this framework to a COVID-19 cohort with varying disease severity and a lung transplant cohort with acute allograft dysfunction. In both contexts, CCC-RISE successfully identified disease-relevant communication programs and traced them to specific cellular subpopulations, often crossing conventional cell-type boundaries. This approach offers a robust pipeline enabling the identification of disease-relevant signaling subpopulations that are invisible to aggregate methods.

bioRxiv (Cold Spring Harbor Laboratory)
University of California, Los Angeles (US), University of California, San Francisco (US), San Francisco VA Health Care System (US), Broad Center (US), UCLA Jonsson Comprehensive Cancer Center
Openalex Percentile: Top 26%
Single-cell and spatial transcriptomics
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