3D-cultured DFAT spheroid-derived exosomes promote aged wound healing via modulation of the NF-κB/Serpine1 pathway.
Abstract
Aging impairs the regenerative capacity of the skin, leading to delayed wound healing and chronic tissue damage. Recent advances have highlighted the therapeutic potential of dedifferentiated fat (DFAT) cells and their secreted exosomes. However, the bioactivity and molecular mechanisms of exosomes derived from DFAT spheroids (DFAT-Sps-Exos) in aging wound repair remain unclear. This study aims to evaluate the regenerative effects of DFAT-Sps-Exos on senescent fibroblasts and aging skin wounds, and to elucidate the underlying molecular mechanisms involved in their activity.
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Research summary
The paper claims that DFAT spheroid-derived exosomes enhance wound healing in aged skin by modulating the NF-κB/Serpine1 pathway. This research is relevant as it explores potential therapeutic strategies targeting the mechanisms of aging to improve regenerative capacity in skin, addressing a fundamental aspect of age-related decline.
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