Macrophage Immunometabolism and Inflammaging: Roles of Mitochondrial Dysfunction, Cellular Senescence, CD38, and NAD.

Johnathan R Yarbro, Russell S Emmons, Brandt D Pence
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引用次数: 27

Abstract

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.

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巨噬细胞免疫代谢和炎症:线粒体功能障碍、细胞衰老、CD38和NAD的作用。
衰老是一个复杂的过程,涉及多个层面的功能障碍,所有这些似乎都集中在炎症上。巨噬细胞与炎症的启动和消退密切相关,它们随着年龄的增长而失调是炎症的主要原因——炎症是一种在衰老过程中发展起来的慢性、低度炎症状态。巨噬细胞发生的与年龄相关的变化包括基础炎症状态的升高和炎症反应的减少或过度活跃,这似乎是由代谢依赖性表观遗传变化驱动的。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和年龄相关的变化,重点是炎症环境、衰老和NAD下降如何影响巨噬细胞的代谢、促进失调,并导致炎症和年龄相关的病理。
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