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微生物群外囊泡通过对 LS174T 杯状细胞三叶因子 3 的差异调节来调节肠道屏障完整性和修复。

Modulation of the Intestinal Barrier Integrity and Repair by Microbiota Extracellular Vesicles through the Differential Regulation of Trefoil Factor 3 in LS174T Goblet Cells.

机构信息

Secció de Bioquímica i Biologia Molecular, Departament de Bioquímica i Fisiologia, Facultat de Farmàcia i Ciències de l'Alimentació, Universitat de Barcelona, 08028 Barcelona, Spain.

Institut de Biomedicina de la Universitat de Barcelona (IBUB), 08028 Barcelona, Spain.

出版信息

Nutrients. 2023 May 24;15(11):2437. doi: 10.3390/nu15112437.

Abstract

Trefoil factor 3 (TFF3) plays a key role in the maintenance and repair of intestinal mucosa. TFF3 expression is upregulated by the microbiota through TLR2. At the posttranscriptional level, TFF3 is downregulated by miR-7-5p. Reduced TFF3 levels have been detected in the damaged tissue of IBD patients. Here, we investigate the regulation of TFF3 expression by microbiota extracellular vesicles (EVs) in LS174T goblet cells using RT-qPCR and inhibitors of the TLR2 or PI3K pathways. To evaluate the subsequent impact on epithelial barrier function, conditioned media from control and vesicle-stimulated LS174T cells were used to treat Caco-2 monolayers. The barrier-strengthening effects were evaluated by analysing the expression and subcellular distribution of tight junction proteins, and the repairing effects were assessed using wound-healing assays. The results showed a differential regulation of TFF3 in LS174T via EVs from the probiotic EcN and the commensal ECOR12. EcN EVs activated the TFF3 production through TLR2 and downregulated miR7-5-p through PI3K. Consistently, high levels of secreted TFF3 reinforced the tight junctions and stimulated wound healing in the Caco-2 cells. ECOR12 EVs did not cause these effects. TFF3 is a potential therapeutic target in IBD. This study contributes to understanding the molecular players (microbiota EVs) connecting gut microbes to health and may help in designing better nutritional interventions based on microbiota bioactive compounds.

摘要

三叶因子 3(TFF3)在维持和修复肠道黏膜中发挥着关键作用。TFF3 的表达受微生物群通过 TLR2 上调。在转录后水平上,TFF3 被 miR-7-5p 下调。在 IBD 患者的受损组织中检测到 TFF3 水平降低。在这里,我们使用 RT-qPCR 和 TLR2 或 PI3K 途径抑制剂研究了微生物群细胞外囊泡(EVs)对 LS174T 杯状细胞中 TFF3 表达的调节。为了评估对上皮屏障功能的后续影响,使用对照和囊泡刺激的 LS174T 细胞的条件培养基处理 Caco-2 单层。通过分析紧密连接蛋白的表达和亚细胞分布来评估增强屏障的作用,通过划痕愈合实验评估修复作用。结果表明,通过益生菌 EcN 和共生菌 ECOR12 的 EVs 对 LS174T 进行了 TFF3 的差异调节。EcN EV 通过 TLR2 激活 TFF3 产生,并通过 PI3K 下调 miR7-5-p。一致地,高水平的分泌型 TFF3 增强了紧密连接并刺激了 Caco-2 细胞中的伤口愈合。ECOR12 EV 没有引起这些效果。TFF3 是 IBD 的潜在治疗靶点。这项研究有助于理解将肠道微生物与健康联系起来的分子参与者(微生物群 EVs),并可能有助于基于微生物群生物活性化合物设计更好的营养干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d8b/10255446/0c5d178a9b11/nutrients-15-02437-g001.jpg

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