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肠道微生物群失调通过代谢产物马尿酸协调白癜风相关的氧化应激。

Gut microbiota dysbiosis orchestrates vitiligo-related oxidative stress through the metabolite hippuric acid.

作者信息

Ni Qingrong, Xia Lin, Huang Ye, Yuan Xiaoying, Gu Weijie, Chen Yueqi, Wang Yijin, Nian Meng, Wu Shengxi, Cai Hong, Huang Jing

机构信息

Department of Dermatology, Air Force Medical Center, Fourth Military Medical University, Beijing, 100142, China.

Department of Neurobiology, Basic Medical Science Academy, Fourth Military Medical University, Xi'an, 710032, China.

出版信息

Microbiome. 2025 May 6;13(1):112. doi: 10.1186/s40168-025-02102-0.

Abstract

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.

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色素脱失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前景的相互作用仍不清楚。

结果

在此,我们比较了白癜风皮损和正常皮肤的转录组数据,发现白癜风皮损中氧化应激相关基因高表达。我们还建立了白癜风小鼠模型,发现肠道微生物群的存在影响了ROS相关基因的表达。肠道微生物群的耗竭减少了黑素细胞中异常的ROS积累和线粒体异常,显著改善了色素脱失。我们通过同笼饲养、粪便微生物群移植(FMT)和补充益生菌来操纵肠道微生物群的研究结果表明,从具有严重白癜风样表型的小鼠转移肠道微生物群会加剧皮肤色素脱失,而益生菌则抑制其进展。对粪便、血清和皮肤组织的靶向代谢组学分析显示,肠道微生物群依赖性的马尿酸积累介导了皮肤中过量的ROS。白癜风患者血清马尿酸水平也得到证实升高。此外,白癜风小鼠肠道通透性的微生物群依赖性增加介导了马尿酸水平的升高,并且我们发现马尿酸可以直接与ROS相关蛋白(NOS2和MAPK14)结合。

结论

我们的结果表明肠道微生物群在调节白癜风表型和氧化应激中起重要作用。我们确定马尿酸是一种肠道微生物群-宿主共代谢产物,是白癜风皮肤氧化应激的关键介质及其结合靶点(NOS2和MAPK14),导致氧化应激。在一小群人类队列中的验证表明,马尿酸可作为白癜风的新型诊断生物标志物和治疗靶点。这些发现为肠道微生物群如何调节白癜风皮肤氧化应激提供了新见解,并提出了该疾病的潜在治疗策略。视频摘要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecd2/12054231/5acdbc6d62db/40168_2025_2102_Fig1_HTML.jpg

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