肠道菌群失调通过代谢产物马尿酸协调白癜风相关的氧化应激。

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Qingrong Ni, Lin Xia, Ye Huang, Xiaoying Yuan, Weijie Gu, Yueqi Chen, Yijin Wang, Meng Nian, Shengxi Wu, Hong Cai, Jing Huang
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引用次数: 0

摘要

背景:白癜风是一种以黑素细胞功能障碍或死亡为特征的脱色性自身免疫性皮肤病,已知与肠道微生物群失衡有关。氧化应激在白癜风的发病机制中起关键作用。然而,皮肤中活性氧(ROS)异常积累与肠道微生物群之间复杂而有希望的相互作用仍不清楚。结果:在这里,我们比较了白癜风病变和正常皮肤的转录组数据,发现白癜风病变中氧化应激相关基因的高表达。我们还建立了白癜风小鼠模型,发现肠道菌群的存在影响ros相关基因的表达。肠道菌群的消耗减少了黑色素细胞中ROS的异常积累和线粒体异常,显著改善了色素沉着。我们通过共住、粪便微生物群移植(FMT)和益生菌补充来控制肠道微生物群的研究结果表明,从患有严重白癜风样表型的小鼠中转移肠道微生物群会加剧皮肤色素沉着,而益生菌会抑制其进展。粪便、血清和皮肤组织的靶向代谢组学显示,肠道微生物依赖于马尿酸的积累,介导皮肤中过量的ROS。白癜风患者血清马尿酸水平升高也得到证实。此外,白癜风小鼠肠道通透性的微生物依赖增加介导了马尿酸水平的升高,我们发现马尿酸可以直接结合ros相关蛋白(NOS2和MAPK14)。结论:肠道菌群在调节白癜风表型和氧化应激中的重要作用。我们发现,作为一种肠道微生物-宿主共代谢物,马尿酸是白癜风皮肤及其结合靶点(NOS2和MAPK14)氧化应激的关键介质,导致氧化应激。在一个小的人类队列验证表明,马尿酸可以作为一种新的诊断生物标志物和治疗白癜风的靶点。这些发现为肠道微生物群如何调节白癜风患者的皮肤氧化应激提供了新的见解,并提出了该病的潜在治疗策略。视频摘要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gut microbiota dysbiosis orchestrates vitiligo-related oxidative stress through the metabolite hippuric acid.

Background: Vitiligo, a depigmenting autoimmune skin disease characterized by melanocyte dysfunction or death, is known to be associated with an imbalance in gut microbiota. Oxidative stress plays a critical role in the pathogenesis of vitiligo. However, the complex promising interaction between abnormal accumulation of reactive oxygen species (ROS) in the skin and gut microbiota has remained unclear.

Results: Here, we compared transcriptome data of vitiligo lesions and normal skin and identified a high expression of oxidative stress-related genes in vitiligo lesions. We also established a vitiligo mouse model and found that the presence of gut microbiota influenced the expression of ROS-related genes. Depletion of gut microbiota reduced abnormal ROS accumulation and mitochondrial abnormalities in melanocytes, significantly improving depigmentation. Our findings from manipulating gut microbiota through cohousing, fecal microbiota transplantation (FMT), and probiotic supplementation showed that transferring gut microbiota from mice with severe vitiligo-like phenotypes exacerbated skin depigmentation while probiotics inhibited its progression. Targeted metabolomics of fecal, serum, and skin tissues revealed gut microbiota-dependent accumulation of hippuric acid, mediating excessive ROS in the skin. Elevated serum hippuric acid levels were also confirmed in vitiligo patients. Additionally, a microbiota-dependent increase in intestinal permeability in vitiligo mice mediated elevated hippuric acid levels, and we found that hippuric acid could directly bind to ROS-related proteins (NOS2 and MAPK14).

Conclusions: Our results suggested the important role of gut microbiota in regulating vitiligo phenotypes and oxidative stress. We identified hippuric acid, a gut microbiota-host co-metabolite, as a critical mediator of oxidative stress in vitiligo skin and its binding targets (NOS2 and MAPK14), resulting in oxidative stress. Validation in a small human cohort suggested that hippuric acid could serve as a novel diagnostic biomarker and therapeutic target for vitiligo. These findings provided new insights into how gut microbiota regulates skin oxidative stress in vitiligo and suggested potential treatment strategies for the disease. Video Abstract.

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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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