Similarities and interplay between senescent cells and macrophages

被引:83
|
作者
Behmoaras, Jacques [1 ]
Gil, Jesus [2 ,3 ]
机构
[1] Imperial Coll London, Hammersmith Hosp, Ctr Inflammatory Dis, London, England
[2] London Inst Med Sci, Med Res Council, London, England
[3] Imperial Coll London, Fac Med, Inst Clin Sci, London, England
来源
JOURNAL OF CELL BIOLOGY | 2021年 / 220卷 / 02期
基金
英国医学研究理事会;
关键词
BETA-GALACTOSIDASE; INFLAMMASOME ACTIVATION; CELLULAR SENESCENCE; MITOCHONDRIAL DYSFUNCTION; OXIDATIVE STRESS; KEY ROLE; PHAGOCYTOSIS; MOUSE; MECHANISMS; DEHYDROGENASE;
D O I
10.1083/jcb.202010162
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Senescence is a cellular program that prevents the replication of old, damaged, or cancerous cells. Senescent cells become growth arrested and undergo changes in their morphology, chromatin organization, and metabolism, and produce a bioactive secretome. This secretome, the senescence-associated secretory phenotype (SASP), mediates many of the pathophysiological effects associated with senescent cells, for example, recruiting and activating immune cells such as macrophages. The relation between senescent cells and macrophages is intriguing: senescent cells recruit macrophages, can induce them to undergo senescence, or can influence their polarization. Senescent cells and macrophages share multiple phenotypic characteristics; both have a high secretory status, increased lysosome numbers, or the ability to activate the inflammasome. Senescent cells accumulate during aging and disease, and killing them results in widespread benefits. Here we discuss similarities between senescent cells and macrophages and interpret the latest developments in macrophage biology to understand the molecular mechanisms of cellular senescence. We describe evidence and effects of senescence in macrophages and speculate on the ontogeny of the senescent-like state in macrophages. Finally, we examine the macrophage-senescent cell interplay and its impact on macrophage effector functions during inflammatory conditions and in the tumor microenvironment.
引用
收藏
页数:8
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