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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...

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Autores principales: Walters, Hannah E., Troyanovskiy, Konstantin E., Graf, Alwin M., Yun, Maximina H.
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
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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.
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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
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