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通过调节RFTN1/脂筏/TLR4介导的炎症来预防慢性化脓性中耳炎

Protects Against Chronic Suppurative Otitis Media via Modulating RFTN1/ Lipid Raft /TLR4-Mediated Inflammation.

作者信息

Liu Zhuohui, Zhang Fan, Jia Fengfeng, Li Shuling, Jiang Chaowu, Ruan Biao, Long Ruiqing

机构信息

Department of Otolaryngology, The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, People's Republic of China.

出版信息

Biologics. 2024 Dec 27;18:453-468. doi: 10.2147/BTT.S484410. eCollection 2024.

Abstract

PURPOSE

Chronic suppurative otitis media (CSOM) is a prominent contributor to preventable hearing loss globally. Probiotic therapy has attracted research interest in human infectious and inflammatory disease. As the most prevalent probiotic, the role of in CSOM remains poorly defined. This study aimed to investigate the antipathogenic effects and underlying mechanism of on CSOM.

METHODS

RNA sequencing of granulation of middle ear cavity from CSOM patients and lavage fluid of middle ear from normal volunteer was conducted. Human middle ear epithelial cells (HMEEC) and rats infected with () and () were used for CSOM constructing. Western blot, qPCR and Vybrant™ Alexa Fluor™ 488 lipid raft labeling were performed to explore the possible molecular mechanism by which lipid raft linker (RFTN1) regulates lipid raft/toll-like receptor 4 (TLR4). ELISA and HE staining was utilized to evaluate the effect of on the progression of CSOM in .

RESULTS

Based on RNA Sequence analysis, a total of 3646 differentially expressed genes (1620 up-regulated and 2026 down-regulated) were identified in CSOM. RFTN1 was highly expressed in CSOM. Inhibition of RFTN1 not only reduced the inflammatory response of CSOM but also suppressed the formation of lipid rafts. Further investigation revealed that RFTN1 inhibition could reduce the expression of TLR4, which also localizes to the lipid rafts. TLR4 responds to RFTN1-mediated inflammatory responses in CSOM. We treated the CSOM model with , which has great potential for alleviating the inflammatory response, and found that attenuated the development of CSOM by reducing RFTN1 and TLR4 expression.

CONCLUSION

In conclusion, these findings suggest a crucial role for in alleviating CSOM progression and uncovered the molecular mechanism involving -regulated inhibition of the RFTN1-lipid raft-TLR4 signaling pathway under CSOM conditions.

摘要

目的

慢性化脓性中耳炎(CSOM)是全球可预防听力损失的一个重要因素。益生菌疗法已引起对人类感染性和炎症性疾病的研究兴趣。作为最普遍的益生菌,其在CSOM中的作用仍不清楚。本研究旨在探讨其对CSOM的抗致病作用及潜在机制。

方法

对CSOM患者中耳腔肉芽组织和正常志愿者中耳灌洗液进行RNA测序。使用人中耳上皮细胞(HMEEC)以及感染了金黄色葡萄球菌(S. aureus)和铜绿假单胞菌(P. aeruginosa)的大鼠构建CSOM模型。进行蛋白质免疫印迹、定量聚合酶链反应和Vybrant™ Alexa Fluor™ 488脂筏标记,以探索脂筏连接蛋白(RFTN1)调节脂筏/ Toll样受体4(TLR4)的可能分子机制。采用酶联免疫吸附测定和苏木精-伊红染色评估其对大鼠CSOM进展情况的影响。

结果

基于RNA序列分析, 在CSOM中总共鉴定出3646个差异表达基因(1620个上调和2026个下调)。RFTN1在CSOM中高表达。抑制RFTN1不仅降低了CSOM的炎症反应,还抑制了脂筏的形成。进一步研究表明,抑制RFTN1可降低同样定位于脂筏的TLR4的表达。TLR4对CSOM中RFTN1介导的炎症反应有应答。我们用具有极大减轻炎症反应潜力的益生菌处理CSOM模型,发现益生菌通过降低RFTN1和TLR4表达减轻了CSOM的发展。

结论

总之,这些发现表明益生菌在减轻CSOM进展中起关键作用,并揭示了在CSOM条件下涉及益生菌调节抑制RFTN1-脂筏-TLR4信号通路的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd6a/11687115/d677d2d4b9e1/BTT-18-453-g0001.jpg

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