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一种口服纳米疗法,通过重塑肠道微生物色氨酸代谢,利用金纳米球为类风湿性关节炎治疗提供支持。

An orally-administered nanotherapeutics with gold nanospheres supplying for rheumatoid arthritis therapy by re-shaping gut microbial tryptophan metabolism.

作者信息

Yang Chuan, Xie Langlang, Deng Zihan, Ai Hongbo, Xiang Tingwen, Yan Xiaojing, Ling Zhiguo, Xiao Shiyu, Tang Yong, Huang Gang, Luo Fei, Chen Yueqi

机构信息

Department of Orthopedics, Southwest Hospital, Third Military Medical University, (Army Medical University), Chongqing, 400038, People's Republic of China.

Department of Biomedical Materials Science, Third Military Medical University, (Army Medical University), Chongqing, 400038, People's Republic of China.

出版信息

J Nanobiotechnology. 2025 May 25;23(1):376. doi: 10.1186/s12951-025-03450-7.

Abstract

Dysbiosis of gut microbiota significantly exacerbates the progression of rheumatoid arthritis (RA). Targeting gut microbiota may present a promising therapeutic strategy for RA. Gold nanospheres (GNS), known for excellent biocompatibility, stability and minimal toxicity, have emerged as precise modulators of gut microbiota, reshaping intestinal environments to treat various inflammatory diseases. Our study found that oral administration of 60-nm GNS effectively ameliorated collagen-induced arthritis (CIA) in mice, with a marked reduction in disease severity and synovial inflammation. Specifically, GNS notably enriched the probiotic genus Ligilactobacillus while restoring intestinal barrier function by upregulating tight junction proteins Claudin-1 and ZO-1. Targeted metabolomics analysis revealed GNS substantially increased the production of indole-3-propionic acid (IPA) and indole-3-acetic acid (IAA) in gut, which were shown to activate the aryl hydrocarbon receptor (AhR) pathway. Mechanistic studies demonstrated that the IPA/IAA mixture inhibited PTEN ubiquitination, stabilizing PTEN protein levels and suppressing NF-κB activation in synovial tissues. These changes correlated with reduced synovial hyperplasia and inflammatory infiltration. Our findings established GNS as an effective nanomodulator of the gut-joint axis, providing novel insights into microbiota-targeted therapies for RA and other inflammatory diseases.

摘要

肠道微生物群失调显著加剧类风湿性关节炎(RA)的进展。针对肠道微生物群可能为RA提供一种有前景的治疗策略。金纳米球(GNS)以其优异的生物相容性、稳定性和极低的毒性而闻名,已成为肠道微生物群的精确调节剂,重塑肠道环境以治疗各种炎症性疾病。我们的研究发现,口服60纳米的GNS可有效改善小鼠胶原诱导的关节炎(CIA),疾病严重程度和滑膜炎症显著减轻。具体而言,GNS显著富集了益生菌利吉乳酸菌属,同时通过上调紧密连接蛋白Claudin-1和ZO-1恢复肠道屏障功能。靶向代谢组学分析表明,GNS显著增加了肠道中吲哚-3-丙酸(IPA)和吲哚-3-乙酸(IAA)的产生,这些物质被证明可激活芳烃受体(AhR)途径。机制研究表明,IPA/IAA混合物抑制PTEN泛素化,稳定PTEN蛋白水平并抑制滑膜组织中的NF-κB激活。这些变化与滑膜增生和炎症浸润减少相关。我们的研究结果确立了GNS作为肠-关节轴的有效纳米调节剂,为RA和其他炎症性疾病的微生物群靶向治疗提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b256/12103761/87bb0f633fb6/12951_2025_3450_Fig1_HTML.jpg

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