A guide to assessing cellular senescencein vitroandin vivo

被引:382
作者
Gonzalez-Gualda, Estela [1 ]
Baker, Andrew G. [2 ]
Fruk, Ljiljana [2 ]
Munoz-Espin, Daniel [1 ]
机构
[1] Univ Cambridge, CRUK Cambridge Ctr, Early Detect Programme, Dept Oncol,Hutchison MRC Res Ctr, Cambridge, England
[2] Univ Cambridge, Dept Chem Engn & Biotechnol, Cambridge, England
基金
英国医学研究理事会;
关键词
ageing; assessment; biomarkers; cellular senescence; detection; DNA-DAMAGE-RESPONSE; BETA-GALACTOSIDASE ACTIVITY; IN-VIVO; HUMAN-CELLS; FIBROBLAST SENESCENCE; IRON ACCUMULATION; TUMOR-SUPPRESSOR; BIOMARKER; INHIBITION; CLEARANCE;
D O I
10.1111/febs.15570
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cellular senescence is a physiological mechanism whereby a proliferating cell undergoes a stable cell cycle arrest upon damage or stress and elicits a secretory phenotype. This highly dynamic and regulated cellular state plays beneficial roles in physiology, such as during embryonic development and wound healing, but it can also result in antagonistic effects in age-related pathologies, degenerative disorders, ageing and cancer. In an effort to better identify this complex state, and given that a universal marker has yet to be identified, a general set of hallmarks describing senescence has been established. However, as the senescent programme becomes more defined, further complexities, including phenotype heterogeneity, have emerged. This significantly complicates the recognition and evaluation of cellular senescence, especially within complex tissues and living organisms. To address these challenges, substantial efforts are currently being made towards the discovery of novel and more specific biomarkers, optimized combinatorial strategies and the development of emerging detection techniques. Here, we compile such advances and present a multifactorial guide to identify and assess cellular senescence in cell cultures, tissues and living organisms. The reliable assessment and identification of senescence is not only crucial for better understanding its underlying biology, but also imperative for the development of diagnostic and therapeutic strategies aimed at targeting senescence in the clinic.
引用
收藏
页码:56 / 80
页数:25
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