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Regulation of cell function and identity by cellular senescence.

Anda HunaAmélie MasseminGabriela MakulyteJean-Michel FlamanNadine MartinDavid Bernard
Published in: The Journal of cell biology (2024)
During aging and in some contexts, like embryonic development, wound healing, and diseases such as cancer, senescent cells accumulate and play a key role in different pathophysiological functions. A long-held belief was that cellular senescence decreased normal cell functions, given the loss of proliferation of senescent cells. This view radically changed following the discovery of the senescence-associated secretory phenotype (SASP), factors released by senescent cells into their microenvironment. There is now accumulating evidence that cellular senescence also promotes gain-of-function effects by establishing, reinforcing, or changing cell identity, which can have a beneficial or deleterious impact on pathophysiology. These effects may involve both proliferation arrest and autocrine SASP production, although they largely remain to be defined. Here, we provide a historical overview of the first studies on senescence and an insight into emerging trends regarding the effects of senescence on cell identity.
Keyphrases
  • induced apoptosis
  • dna damage
  • endothelial cells
  • cell cycle arrest
  • stress induced
  • single cell
  • signaling pathway
  • cell therapy
  • cell death
  • small molecule
  • high throughput
  • cell proliferation
  • young adults
  • bone marrow