Spatially structured inflammatory response in the presence of a uniform stimulus

Inflammatory responses occur within the complex spatial context of tissues and organs, and many questions remain about how tissue structure and cellular communication shape their spatiotemporal dynamics. Here, we use a multiplexed RNA in situ hybridization approach, together with analytical tools, to study inflammatory gene expression in the larval zebrafish tailfin in response to a bath of lipopolysaccharide. We use this model system to address whether spatial structure emerges in the tissue response even absent the spatial variation introduced by a pathogen. We find that epithelial cells in the tailfin express several proinflammatory genes, and that across these genes, the uniform stimulus triggers a spatially nonuniform response. We use a graph-based spectral decomposition method to analyze its structure, and find that it is consistent with a diffusion-consumption model of secondary signaling. Overall, long-wavelength modes dominate the signal, creating zones of activation which account for a majority of the variation in gene expression. Our results show that epithelial cells are important producers of proinflammatory effector molecules in this system, and that tissue induces spatial correlations even absent a structured input.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2026-03-20
DOI
https://doi.org/10.1073/pnas.2507102123
Primary Topic
Single-cell and spatial transcriptomics
Type
article
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article

Spatially structured inflammatory response in the presence of a uniform stimulus

Elizabeth R. Jerison, Nicolas Romeo, Stephen R. Quake
Proceedings of the National Academy of Sciences
Single-cell and spatial transcriptomics
article

Spatially structured inflammatory response in the presence of a uniform stimulus

Elizabeth R. Jerison, Nicolas Romeo, Stephen R. Quake
article en

Abstract

Inflammatory responses occur within the complex spatial context of tissues and organs, and many questions remain about how tissue structure and cellular communication shape their spatiotemporal dynamics. Here, we use a multiplexed RNA in situ hybridization approach, together with analytical tools, to study inflammatory gene expression in the larval zebrafish tailfin in response to a bath of lipopolysaccharide. We use this model system to address whether spatial structure emerges in the tissue response even absent the spatial variation introduced by a pathogen. We find that epithelial cells in the tailfin express several proinflammatory genes, and that across these genes, the uniform stimulus triggers a spatially nonuniform response. We use a graph-based spectral decomposition method to analyze its structure, and find that it is consistent with a diffusion-consumption model of secondary signaling. Overall, long-wavelength modes dominate the signal, creating zones of activation which account for a majority of the variation in gene expression. Our results show that epithelial cells are important producers of proinflammatory effector molecules in this system, and that tissue induces spatial correlations even absent a structured input.

Proceedings of the National Academy of SciencesVol. 123(12)
University of Chicago (US), Systems Dynamics (United States) (US), James Lind Institute (CH), Living Systems (United States) (US), Stanford University (US)
Openalex Percentile: Top 14%
Single-cell and spatial transcriptomics
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