Department of Microbiology and Immunology, Room #3146A, University of Miami Miller School of Medicine, P.O. Box 016960 (R-138), Miami, FL 33101, USA..
Exp Gerontol. 2018 Jul 1;107:55-58. doi: 10.1016/j.exger.2017.07.002. Epub 2017 Jul 4.
Immune cells with a senescence-associated secretory phenotype increase in the blood of elderly individuals or individuals with age-associated diseases or with infections. Although senescent immune cells do not proliferate, they are transcriptionally and metabolically active and affect the microenvironment through the secretion of pro-inflammatory mediators. An age-driven increase in senescent B, T and NK cells has been reported and the function of these cells has been characterized. Results published by different groups have demonstrated that cell senescence induces the accumulation of terminally-differentiated cells characterized by the arrest of cell proliferation but with an active secretory profile which regulates their function through the activation of pathways integrating senescence and energy-sensing signals. This review will focus on senescent B cells, their increase in aging, age-associated conditions and infections. Similarities with other senescent immune cells will be presented and discussed.
衰老相关分泌表型的免疫细胞在老年人或与年龄相关疾病或感染患者的血液中增加。尽管衰老的免疫细胞不再增殖,但它们在转录和代谢上仍然活跃,并通过分泌促炎介质来影响微环境。已经报道了衰老的 B、T 和 NK 细胞随年龄的增长而增加,并且已经对这些细胞的功能进行了描述。不同研究小组发表的结果表明,细胞衰老会诱导终末分化细胞的积累,这些细胞的特征是细胞增殖停滞,但具有活跃的分泌特征,通过激活整合衰老和能量感应信号的途径来调节其功能。这篇综述将重点关注衰老的 B 细胞及其在衰老、与年龄相关的疾病和感染中的增加。还将介绍并讨论与其他衰老免疫细胞的相似之处。