Fibroblast state switching orchestrates dermal maturation and wound healing

Murine dermis contains functionally and spatially distinct fibroblast lineages that cease to proliferate in early postnatal life. Here we propose a model in which a negative feedback loop between extracellular matrix (ECM) deposition and fibroblast proliferation determines dermal architecture. Virtual-tissue simulations of our model faithfully recapitulate dermal maturation, predicting a loss of spatial segregation of fibroblast lineages and dictating that fibroblast migration is only required for wound healing. To test this, we performed in vivo live imaging of dermal fibroblasts, which revealed that homeostatic tissue architecture is achieved without active cell migration. In contrast, both fibroblast proliferation and migration are key determinants of tissue repair following wounding. The results show that tissue-scale coordination is driven by the interdependence of cell proliferation and ECM deposition, paving the way for identifying new therapeutic strategies to enhance skin regeneration.\n\nStandfirst textWe show that fibroblast behaviour switching between two distinct states - proliferating and depositing ECM - is necessary and sufficient to define dermal architecture. Understanding this interdependence is critical for identifying new therapeutic strategies to enhance skin regeneration.\n\nHighlightsO_LITissue-scale coordination in murine dermis is driven by the interdependence of cell proliferation and ECM deposition\nC_LIO_LIThe tissue architecture is set by a negative feedback loop between ECM deposition/remodelling and proliferation\nC_LIO_LIFibroblast lineages lose segregation with age\nC_LIO_LIFibroblast migration is the critical discriminator between dermal development and wound healing\nC_LI