衰老
巨噬细胞
炎症
生物
自噬
表型
巨噬细胞极化
免疫学
吞噬作用
抗原呈递
免疫系统
适应不良
细胞生物学
遗传学
T细胞
细胞凋亡
基因
体外
作者
Longling Wang,Wenxiang Hong,Hong Zhu,Qiaojun He,Bo Yang,Jiajia Wang,Qinjie Weng
标识
DOI:10.1016/j.apsb.2024.01.008
摘要
Macrophage senescence, manifested by the special form of durable cell cycle arrest and chronic low-grade inflammation like senescence-associated secretory phenotype, has long been considered harmful. Persistent senescence of macrophages may lead to maladaptation, immune dysfunction, and finally the development of age-related diseases, infections, autoimmune diseases, and malignancies. However, it is a ubiquitous, multi-factorial, and dynamic complex phenomenon that also plays roles in remodeled processes, including wound repair and embryogenesis. In this review, we summarize some general molecular changes and several specific biomarkers during macrophage senescence, which may bring new sight to recognize senescent macrophages in different conditions. Also, we take an in-depth look at the functional changes in senescent macrophages, including metabolism, autophagy, polarization, phagocytosis, antigen presentation, and infiltration or recruitment. Furthermore, some degenerations and diseases associated with senescent macrophages as well as the mechanisms or relevant genetic regulations of senescent macrophages are integrated, not only emphasizing the possibility of regulating macrophage senescence to benefit age-associated diseases but also has an implication on the finding of potential targets or drugs clinically.
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