乳酸菌通过调节RFTN1/脂质筏/ tlr4介导的炎症来预防慢性化脓性中耳炎。

IF 5.3 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Biologics : Targets & Therapy Pub Date : 2024-12-27 eCollection Date: 2024-01-01 DOI:10.2147/BTT.S484410
Zhuohui Liu, Fan Zhang, Fengfeng Jia, Shuling Li, Chaowu Jiang, Biao Ruan, Ruiqing Long
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引用次数: 0

摘要

目的:慢性化脓性中耳炎(CSOM)是全球可预防性听力损失的主要原因。益生菌治疗已成为人类感染性和炎症性疾病的研究热点。作为最普遍的益生菌,乳酸菌在CSOM中的作用尚未明确。本研究旨在探讨乳酸菌对CSOM的抗病原菌作用及其机制。方法:对CSOM患者中耳腔肉芽和正常志愿者中耳灌洗液进行RNA测序。采用蜡样芽孢杆菌(B. cereus)和金黄色葡萄球菌(S. aureus)感染的人中耳上皮细胞(HMEEC)和大鼠进行CSOM构建。通过Western blot、qPCR和Vybrant™Alexa Fluor™488脂筏标记来探索脂筏连接子(RFTN1)调节脂筏/toll样受体4 (TLR4)的可能分子机制。ELISA法和HE染色法检测乳酸菌对CSOM进展的影响。结果:基于RNA序列分析,在CSOM中共鉴定出3646个差异表达基因,其中上调1620个,下调2026个。RFTN1在CSOM中高表达。抑制RFTN1不仅可以降低CSOM的炎症反应,还可以抑制脂筏的形成。进一步研究发现,抑制RFTN1可降低TLR4的表达,TLR4也定位于脂筏。TLR4响应rftn1介导的CSOM炎症反应。我们用乳酸菌处理CSOM模型,乳酸菌具有很大的减轻炎症反应的潜力,发现乳酸菌通过降低RFTN1和TLR4的表达来减轻CSOM的发展。结论:综上所述,这些发现提示乳酸菌在缓解CSOM进展中发挥了重要作用,并揭示了CSOM条件下乳酸菌调节抑制rftn1 -脂质筏- tlr4信号通路的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lactobacillus Protects Against Chronic Suppurative Otitis Media via Modulating RFTN1/ Lipid Raft /TLR4-Mediated Inflammation.

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 Lactobacillus in CSOM remains poorly defined. This study aimed to investigate the antipathogenic effects and underlying mechanism of Lactobacillus 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 Bacillus cereus (B. cereus) and Staphylococcus aureus (S. aureus) 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 Lactobacillus on the progression of CSOM in vivo.

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 Lactobacillus, which has great potential for alleviating the inflammatory response, and found that Lactobacillus attenuated the development of CSOM by reducing RFTN1 and TLR4 expression.

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

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来源期刊
Biologics : Targets & Therapy
Biologics : Targets & Therapy MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
8.30
自引率
0.00%
发文量
22
审稿时长
16 weeks
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