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.
Jerison et al. (Fri,) studied this question.