Fanning the Flames of Inflammaging: Impact of Monocyte Metabolic Reprogramming.

Immunometabolism Pub Date : 2020-01-01 Epub Date: 2020-07-01 DOI:10.20900/immunometab20200025
Brandt D Pence
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Abstract

Monocytes are circulating innate immune cells that are functionally dysregulated during aging. However, while metabolic regulation of innate immune cell function is now well-established, only a handful of studies have examined this in the context of aging. In a recent article published in Aging Cell, Saare et al. observe comprehensive metabolic reprogramming of otherwise unstimulated monocytes isolated from older adults. These cells display increased glucose uptake and dysregulation of mitochondrial function, concomitant with activation of signaling pathways contributing to increased inflammation. These findings suggest a mechanism whereby metabolic reprogramming in aged monocytes contributes to chronic low-grade inflammation and open new avenues of investigation into the biological underpinning of inflammaging.

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煽起炎症的火焰:单核细胞代谢重编程的影响。
单核细胞是循环中的先天性免疫细胞,在衰老过程中会出现功能失调。然而,尽管先天性免疫细胞功能的代谢调节现已得到证实,但只有少数研究在衰老的背景下对此进行了研究。在最近发表于《衰老细胞》(Aging Cell)的一篇文章中,Saare 等人观察到从老年人体内分离出来的单核细胞进行了全面的代谢重编程。这些细胞表现出葡萄糖摄取增加和线粒体功能失调,同时信号通路被激活,导致炎症加剧。这些发现提示了老年单核细胞代谢重编程导致慢性低度炎症的机制,并为研究炎症的生物学基础开辟了新的途径。
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