Your new experience awaits. Try the new design now and help us make it even better

REVIEW article

Front. Cell Dev. Biol.

Sec. Stem Cell Research

This article is part of the Research TopicSkeletal Muscle Aging and Stem CellsView all articles

The Impact of Cellular Senescence on Aging Skeletal Muscle

Provisionally accepted
Michael  KamalMichael KamalRyan  BevingtonRyan BevingtonAmanda  JohnsonAmanda JohnsonGianni  PariseGianni Parise*
  • McMaster University, Hamilton, Canada

The final, formatted version of the article will be published soon.

Skeletal muscle is a highly plastic tissue that relies on its resident muscle stem cell population, known as satellite cells (MuSC), for its timely repair and regeneration. During aging, there is a decline in muscle regenerative capacity that is largely attributed to the loss of MuSC content and function. These aberrations are thought to contribute to the aging-related decline in skeletal muscle mass and strength. Cellular senescence, which is characterized by a state of irreversible cell cycle arrest and the presence of a senescence-associated secretory phenotype (SASP), has emerged as a potential factor in the dysfunction of MuSCs with aging. Much effort has recently been made to examine the detrimental effects of senescence on skeletal muscle as well as identify therapeutic approaches to selectively eliminate these cells and improve the aging phenotype. Here, we discuss the current understanding of aging-related MuSC impairments and the underlying mechanisms that link cellular senescence to the decline in muscle regenerative capacity.

Keywords: cellular senescence, Aging, skeletal muscle, Regeneration, satellite cells, SASP, senolytics

Received: 06 Oct 2025; Accepted: 17 Nov 2025.

Copyright: © 2025 Kamal, Bevington, Johnson and Parise. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Gianni Parise, pariseg@mcmaster.ca

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.