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Cellular senescence and the skeleton: pathophysiology and therapeutic implications

Cellular senescence is a fundamental aging mechanism that is currently the focus of considerable interest as a pathway that could be targeted to ameliorate aging across multiple tissues, including the skeleton. There is now substantial evidence that senescent cells accumulate in the bone microenviro...

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Detalles Bibliográficos
Autores principales: Khosla, Sundeep, Farr, Joshua N., Monroe, David G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803328/
https://www.ncbi.nlm.nih.gov/pubmed/35104801
http://dx.doi.org/10.1172/JCI154888
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author Khosla, Sundeep
Farr, Joshua N.
Monroe, David G.
author_facet Khosla, Sundeep
Farr, Joshua N.
Monroe, David G.
author_sort Khosla, Sundeep
collection PubMed
description Cellular senescence is a fundamental aging mechanism that is currently the focus of considerable interest as a pathway that could be targeted to ameliorate aging across multiple tissues, including the skeleton. There is now substantial evidence that senescent cells accumulate in the bone microenvironment with aging and that targeting these cells prevents age-related bone loss, at least in mice. Cellular senescence also plays important roles in mediating the skeletal fragility associated with diabetes mellitus, radiation, and chemotherapy. As such, there are ongoing efforts to develop “senolytic” drugs that kill senescent cells by targeting key survival mechanisms in these cells without affecting normal cells. Because senescent cells accumulate across tissues with aging, senolytics offer the attractive possibility of treating multiple age-related comorbidities simultaneously.
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spelling pubmed-88033282022-02-04 Cellular senescence and the skeleton: pathophysiology and therapeutic implications Khosla, Sundeep Farr, Joshua N. Monroe, David G. J Clin Invest Review Cellular senescence is a fundamental aging mechanism that is currently the focus of considerable interest as a pathway that could be targeted to ameliorate aging across multiple tissues, including the skeleton. There is now substantial evidence that senescent cells accumulate in the bone microenvironment with aging and that targeting these cells prevents age-related bone loss, at least in mice. Cellular senescence also plays important roles in mediating the skeletal fragility associated with diabetes mellitus, radiation, and chemotherapy. As such, there are ongoing efforts to develop “senolytic” drugs that kill senescent cells by targeting key survival mechanisms in these cells without affecting normal cells. Because senescent cells accumulate across tissues with aging, senolytics offer the attractive possibility of treating multiple age-related comorbidities simultaneously. American Society for Clinical Investigation 2022-02-01 2022-02-01 /pmc/articles/PMC8803328/ /pubmed/35104801 http://dx.doi.org/10.1172/JCI154888 Text en © 2022 Khosla et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review
Khosla, Sundeep
Farr, Joshua N.
Monroe, David G.
Cellular senescence and the skeleton: pathophysiology and therapeutic implications
title Cellular senescence and the skeleton: pathophysiology and therapeutic implications
title_full Cellular senescence and the skeleton: pathophysiology and therapeutic implications
title_fullStr Cellular senescence and the skeleton: pathophysiology and therapeutic implications
title_full_unstemmed Cellular senescence and the skeleton: pathophysiology and therapeutic implications
title_short Cellular senescence and the skeleton: pathophysiology and therapeutic implications
title_sort cellular senescence and the skeleton: pathophysiology and therapeutic implications
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803328/
https://www.ncbi.nlm.nih.gov/pubmed/35104801
http://dx.doi.org/10.1172/JCI154888
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