T细胞炎症和衰老过程中的代谢重编程

Alessio Bevilacqua, Ping-Chih Ho, F. Franco
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引用次数: 1

摘要

由于对病原体的免疫反应下降、疫苗接种效力减弱和组织稳态紊乱,衰老对公共卫生构成了新的挑战。细胞和系统水平的代谢变化也是衰老的主要特征。此外,细胞代谢已经出现,通过调节信号级联和表观遗传学景观来提供指导免疫细胞行为的调节,免疫细胞中异常的衰老过程可以导致炎症,这是一种慢性和低度炎症,通过干扰组织和器官的稳态来促进衰老。在这里,我们回顾了衰老过程如何影响T细胞的代谢程序,以及衰老的T细胞如何调节炎症。此外,我们还讨论了通过重新连接免疫细胞的代谢程序来逆转或改善衰老的潜在方法。
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Metabolic reprogramming in inflammaging and aging in T cells
Aging represents an emerging challenge for public health due to the declined immune responses against pathogens, weakened vaccination efficacy, and disturbed tissue homeostasis. Metabolic alterations in cellular and systemic levels are also known to be cardinal features of aging. Moreover, cellular metabolism has emerged to provide regulations to guide immune cell behavior via modulations on signaling cascades and epigenetic landscape, and aberrant aging process in immune cells can lead to inflammaging, a chronic and low-grade inflammation that facilitates aging by perturbing homeostasis in tissues and organs. Here, we review how metabolic program in T cells is influenced by aging process and how aged T cells modulate inflammaging. In addition, we discuss the potential approaches to reverse or ameliorate aging by rewiring metabolic programming of immune cells.
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