Yarbro Johnathan R, Emmons Russell S, Pence Brandt D
School of Health Studies, University of Memphis, Memphis, TN 38152, USA.
Bioinformatics Program, University of Memphis, Memphis, TN 38152, USA.
Immunometabolism. 2020;2(3):e200026. doi: 10.20900/immunometab20200026. Epub 2020 Jul 1.
Aging is a complex process that involves dysfunction on multiple levels, all of which seem to converge on inflammation. Macrophages are intimately involved in initiating and resolving inflammation, and their dysregulation with age is a primary contributor to inflammaging-a state of chronic, low-grade inflammation that develops during aging. Among the age-related changes that occur to macrophages are a heightened state of basal inflammation and diminished or hyperactive inflammatory responses, which seem to be driven by metabolic-dependent epigenetic changes. In this review article we provide a brief overview of mitochondrial functions and age-related changes that occur to macrophages, with an emphasis on how the inflammaging environment, senescence, and NAD decline can affect their metabolism, promote dysregulation, and contribute to inflammaging and age-related pathologies.
衰老过程复杂,涉及多个层面的功能失调,而这一切似乎都与炎症相关。巨噬细胞密切参与炎症的启动和消退过程,随着年龄增长,巨噬细胞的失调是引发炎症衰老(一种在衰老过程中出现的慢性、低度炎症状态)的主要因素。巨噬细胞发生的与年龄相关的变化包括基础炎症状态增强以及炎症反应减弱或亢进,这些变化似乎是由代谢依赖性表观遗传变化所驱动的。在这篇综述文章中,我们简要概述了巨噬细胞的线粒体功能及与年龄相关的变化,重点阐述炎症衰老环境、细胞衰老和烟酰胺腺嘌呤二核苷酸(NAD)水平下降如何影响巨噬细胞的代谢、导致调节失调,并促使炎症衰老及与年龄相关的病理状况的发生。