Young gut microbiota transplantation improves the metabolic health of old mice.

IF 5 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2025-05-30 DOI:10.1128/msystems.01601-24
Jiaojiao Xie, Taewan Kim, Zhongmao Liu, Hunter Panier, Suresh Bokoliya, Ming Xu, Yanjiao Zhou
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引用次数: 0

Abstract

The gut microbiota evolves over a lifetime and significantly impacts the aging process. Targeting the gut microbiota represents a novel avenue to delay aging and aging-related physical and mental decline. However, the underlying mechanism by which the microbiota modulates the aging process, particularly age-related physical and behavioral changes is not completely understood. We conducted fecal microbiota transplantation (FMT) from young or old male donor mice to the old male recipients. Old recipients with young microbiota had a higher alpha diversity than the old recipients with old microbiota. Compared to FMT with old microbiota, FMT with young microbiota reduced body weight and prevented fat accumulation in the old recipients. FMT with young microbiota also lowered frailty, increased grip strength, and alleviated depression and anxiety-like behavior in the old recipients. Consistent with observed physical changes, untargeted metabolomic analysis of serum and stools revealed that FMT with young microbiota lowered age-related long-chain fatty acid levels and increased amino acid levels in the old recipients. Bulk RNAseq analysis of the amygdala of the brain showed that FMT with young microbiota downregulated inflammatory pathways and upregulated oxidative phosphorylation in the old recipients. Our results demonstrate that FMT with young microbiota has substantial positive influences on age-related body composition, frailty, and psychological behaviors. These effects are associated with changes in host lipid and amino acid metabolism in the periphery and transcriptional regulation of neuroinflammation and energy utilization in the brain.

Importance: The gut microbiome is a key hallmark of aging. Fecal microbiota transplantation (FMT) using young microbiota represents a novel rejuvenation strategy to delay aging. Our study provides compelling evidence that transplanting microbiota from young mice significantly improved grip strength, frailty, and body composition in aged recipient mice. At the molecular level, FMT improved aging-related metabolic markers in the gut and circulation. Additionally, FMT from young microbiota rejuvenated the amygdala of the aged brain by downregulating inflammatory pathways. This study highlights the importance of metabolic reprogramming via young microbiota FMT in improving physical and metabolic health in elderly recipients.

年轻肠道菌群移植可改善老年小鼠的代谢健康。
肠道菌群在一生中不断进化,并对衰老过程产生重大影响。针对肠道微生物群是延缓衰老和衰老相关的身心衰退的新途径。然而,微生物群调节衰老过程的潜在机制,特别是与年龄相关的身体和行为变化,尚不完全清楚。我们将年轻或老年雄性供鼠的粪便微生物群移植给老年雄性受体。具有年轻微生物群的老年受者α多样性高于具有年老微生物群的老年受者。与具有老微生物群的FMT相比,具有年轻微生物群的FMT降低了老年接受者的体重并防止了脂肪堆积。具有年轻微生物群的FMT也降低了老年接受者的脆弱性,增加了握力,减轻了抑郁和焦虑样行为。与观察到的身体变化一致,血清和粪便的非靶向代谢组学分析显示,年轻微生物群的FMT降低了老年受体中与年龄相关的长链脂肪酸水平,并增加了氨基酸水平。大脑杏仁核的大量RNAseq分析显示,年轻微生物群的FMT下调了老年受体的炎症途径并上调了氧化磷酸化。我们的研究结果表明,具有年轻微生物群的FMT对与年龄相关的身体成分,脆弱性和心理行为具有实质性的积极影响。这些作用与宿主脂质和外周氨基酸代谢的变化以及神经炎症和大脑能量利用的转录调节有关。重要性:肠道微生物群是衰老的关键标志。利用年轻的微生物群进行粪便微生物群移植(FMT)是一种新的延缓衰老的再生策略。我们的研究提供了令人信服的证据,证明从年轻小鼠身上移植的微生物群显著改善了老年受体小鼠的握力、虚弱和身体成分。在分子水平上,FMT改善了肠道和循环中与衰老相关的代谢标志物。此外,来自年轻微生物群的FMT通过下调炎症通路使衰老大脑的杏仁核恢复活力。本研究强调了通过年轻微生物群FMT进行代谢重编程在改善老年受者身体和代谢健康方面的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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