Abstract

Impaired stem cell functions, which gradually fail to replenish damaged and senescent cells in distinct organ parenchyma can lead to tissue atrophy and organ aging. This failure can either be due to an intrinsic dysfunction of stem/progenitor cells, the disruption of the corresponding stem cell niche, or a combination of both. Fibroblasts in the connective tissue region of many organs, such as skin, contribute to the formation of stem cell niche. Though the impact of the connective tissue resident fibroblasts on stem cell niches and organ aging is an emerging concept, the underlying mechanisms are largely unexplored.

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