SPP1 and Duchenne muscular dystrophy: Similarly, in Duchenne muscular dystrophy (DMD) mouse models, integrated Visium spatial and single‐cell transcriptomics revealed FAP expansion and CCC networks emanating from dystrophic regions, with distinct inflammatory (Ccl2, Ccl7, and Spp1) and regenerative‐like enriched collagen expressing FAPs clusters [21].