Giroud Joëlle, Combémorel Emilie, Pourtier Albin, Abbadie Corinne, Pluquet Olivier
CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, UMR9020-U1277-CANTHER-Cancer Heterogeneity, Plasticity and Resistance to Therapies, University of Lille, Lille, France.
Am J Physiol Cell Physiol. 2025 Jun 1;328(6):C1764-C1782. doi: 10.1152/ajpcell.00091.2025. Epub 2025 Apr 21.
Senescence is a complex cellular state that can be considered as a stress response phenotype. A decade ago, we suggested the intricate connections between unfolded protein response (UPR) signaling and the development of the senescent phenotype. Over the past ten years, significant advances have been made in understanding the multifaceted role of the UPR in regulating cellular senescence, highlighting its contribution to biological processes such as oxidative stress and autophagy. In this updated review, we expand these interconnections with the benefit of new insights, and we suggest that targeting specific components of the UPR could provide novel therapeutic strategies to mitigate the deleterious effects of senescence, with significant implications for age-related pathologies and geroscience.
衰老 是一种复杂的细胞状态,可被视为一种应激反应表型。十年前,我们提出了未折叠蛋白反应(UPR)信号与衰老表型发展之间的复杂联系。在过去十年中,在理解UPR在调节细胞衰老中的多方面作用方面取得了重大进展,突出了其对氧化应激和自噬等生物学过程的贡献。在这篇更新的综述中,我们借助新的见解扩展了这些相互联系,并提出靶向UPR的特定成分可以提供新的治疗策略,以减轻衰老的有害影响,这对与年龄相关的病理学和老年科学具有重要意义。