{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nMatrix metalloproteinase‐10 (MMP10, also known as stromelysin‐2) is emerging as a key mediator of physiological tissue remodeling and inflammatory responses. In cutaneous wounds, for example, MMP10 is up‐regulated in keratinocytes to finely modulate extracellular matrix degradation, thereby facilitating proper keratinocyte migration and re‐epithelialization. In parallel, studies in liver, skeletal muscle, kidney, bone and peritoneal tissues demonstrate that MMP10 supports regeneration by promoting angiogenesis, orchestrating matrix turnover, and indirectly controlling leukocyte recruitment and activation during acute injury and infection. 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