Cargando…
Senescent cells enhance newt limb regeneration by promoting muscle dedifferentiation
Salamanders are able to regenerate their entire limbs throughout lifespan, through a process that involves significant modulation of cellular plasticity. Limb regeneration is accompanied by the endogenous induction of cellular senescence, a state of irreversible cell cycle arrest associated with pro...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265169/ https://www.ncbi.nlm.nih.gov/pubmed/37025070 http://dx.doi.org/10.1111/acel.13826 |
_version_ | 1785058476866666496 |
---|---|
author | Walters, Hannah E. Troyanovskiy, Konstantin E. Graf, Alwin M. Yun, Maximina H. |
author_facet | Walters, Hannah E. Troyanovskiy, Konstantin E. Graf, Alwin M. Yun, Maximina H. |
author_sort | Walters, Hannah E. |
collection | PubMed |
description | Salamanders are able to regenerate their entire limbs throughout lifespan, through a process that involves significant modulation of cellular plasticity. Limb regeneration is accompanied by the endogenous induction of cellular senescence, a state of irreversible cell cycle arrest associated with profound non‐cell‐autonomous consequences. While traditionally associated with detrimental physiological effects, here, we show that senescent cells can enhance newt limb regeneration. Through a lineage tracing approach, we demonstrate that exogenously derived senescent cells promote dedifferentiation of mature muscle tissue to generate regenerative progenitors. In a paradigm of newt myotube dedifferentiation, we uncover that senescent cells promote myotube cell cycle re‐entry and reversal of muscle identity via secreted factors. Transcriptomic profiling and loss of function approaches identify the FGF‐ERK signalling axis as a critical mediator of senescence‐induced muscle dedifferentiation. While chronic senescence constrains muscle regeneration in physiological mammalian contexts, we thus highlight a beneficial role for cellular senescence as an important modulator of dedifferentiation, a key mechanism for regeneration of complex structures. |
format | Online Article Text |
id | pubmed-10265169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102651692023-06-15 Senescent cells enhance newt limb regeneration by promoting muscle dedifferentiation Walters, Hannah E. Troyanovskiy, Konstantin E. Graf, Alwin M. Yun, Maximina H. Aging Cell Research Articles Salamanders are able to regenerate their entire limbs throughout lifespan, through a process that involves significant modulation of cellular plasticity. Limb regeneration is accompanied by the endogenous induction of cellular senescence, a state of irreversible cell cycle arrest associated with profound non‐cell‐autonomous consequences. While traditionally associated with detrimental physiological effects, here, we show that senescent cells can enhance newt limb regeneration. Through a lineage tracing approach, we demonstrate that exogenously derived senescent cells promote dedifferentiation of mature muscle tissue to generate regenerative progenitors. In a paradigm of newt myotube dedifferentiation, we uncover that senescent cells promote myotube cell cycle re‐entry and reversal of muscle identity via secreted factors. Transcriptomic profiling and loss of function approaches identify the FGF‐ERK signalling axis as a critical mediator of senescence‐induced muscle dedifferentiation. While chronic senescence constrains muscle regeneration in physiological mammalian contexts, we thus highlight a beneficial role for cellular senescence as an important modulator of dedifferentiation, a key mechanism for regeneration of complex structures. John Wiley and Sons Inc. 2023-04-06 /pmc/articles/PMC10265169/ /pubmed/37025070 http://dx.doi.org/10.1111/acel.13826 Text en © 2023 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Walters, Hannah E. Troyanovskiy, Konstantin E. Graf, Alwin M. Yun, Maximina H. Senescent cells enhance newt limb regeneration by promoting muscle dedifferentiation |
title | Senescent cells enhance newt limb regeneration by promoting muscle dedifferentiation |
title_full | Senescent cells enhance newt limb regeneration by promoting muscle dedifferentiation |
title_fullStr | Senescent cells enhance newt limb regeneration by promoting muscle dedifferentiation |
title_full_unstemmed | Senescent cells enhance newt limb regeneration by promoting muscle dedifferentiation |
title_short | Senescent cells enhance newt limb regeneration by promoting muscle dedifferentiation |
title_sort | senescent cells enhance newt limb regeneration by promoting muscle dedifferentiation |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265169/ https://www.ncbi.nlm.nih.gov/pubmed/37025070 http://dx.doi.org/10.1111/acel.13826 |
work_keys_str_mv | AT waltershannahe senescentcellsenhancenewtlimbregenerationbypromotingmusclededifferentiation AT troyanovskiykonstantine senescentcellsenhancenewtlimbregenerationbypromotingmusclededifferentiation AT grafalwinm senescentcellsenhancenewtlimbregenerationbypromotingmusclededifferentiation AT yunmaximinah senescentcellsenhancenewtlimbregenerationbypromotingmusclededifferentiation |