Age-related alterations in gut homeostasis are microbiota dependent.

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yingli Jing, Qiuying Wang, Fan Bai, Zihan Li, Yan Li, Weijin Liu, Yitong Yan, Shuangyue Zhang, Chen Gao, Yan Yu
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引用次数: 0

Abstract

Accumulating data suggest that remodeling aged gut microbiota improves aging-related imbalance in intestinal homeostasis. However, evidence in favor of the beneficial effect of remodeling gut microbiota on intestinal stress and immune responses during aging is scarce. The current study revealed that old mice presented impaired gut barrier integrity. Transcriptome sequencing coupled with bioinformatics analysis revealed that aging altered gene expression profiles of the colon and mesenteric lymph nodes, which are involved mainly in stress and immune responses, respectively. Notably, gut microbiota was closely related to the differentially expressed genes. Microbiota depletion in old mice ameliorated gut barrier integrity and partially reversed the inflammatory factors upregulated in aging mice. Furthermore, fecal microbiota transplantation from young mice to old mice resulted in a significant improvement in intestinal barrier integrity and immune homeostasis. These findings highlight the potential of microbiota-targeted interventions on aging-related physiological processes and call for further investigation.

与年龄相关的肠道内稳态改变依赖于微生物群。
越来越多的数据表明,重塑衰老的肠道微生物群可以改善与衰老相关的肠道内稳态失衡。然而,支持肠道微生物群重塑对衰老过程中肠道应激和免疫反应有益作用的证据很少。目前的研究表明,老年小鼠表现出肠道屏障完整性受损。转录组测序结合生物信息学分析显示,衰老改变了结肠和肠系膜淋巴结的基因表达谱,这两个淋巴结分别主要参与应激和免疫反应。值得注意的是,肠道菌群与差异表达基因密切相关。老年小鼠的微生物群消耗改善了肠道屏障的完整性,并部分逆转了衰老小鼠中上调的炎症因子。此外,从年轻小鼠到老年小鼠的粪便微生物群移植导致肠道屏障完整性和免疫稳态的显着改善。这些发现强调了以微生物群为目标干预衰老相关生理过程的潜力,并呼吁进一步研究。
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
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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