Division of Gastroenterology-Hepatology, Department of Internal Medicine, Maastricht University Medical Centre, Maastricht, The Netherlands.
School of Nutrition and Translational Research in Metabolism, Maastricht University Medical Center, Maastricht, The Netherlands.
Sci Rep. 2019 Feb 14;9(1):2030. doi: 10.1038/s41598-018-38322-8.
Intestinal epithelial barrier is affected by multiple factors, such as tumour necrosis factor-α (TNF-α). Plasma concentration of TNF-α is higher in patients with Crohn's disease (CD) than healthy controls (HC) and correlates positively with disease activity. This study aimed to determine the effect of plasma from active, inactive CD patients on intestinal barrier function and to investigate the underlying mechanism. Plasma samples were collected from CD patients and HC. 3D Caco-2 cysts were treated with plasma or TNF-α, with or without pre-incubation of adalimumab (a monoclonal antibody that antagonizes TNF-α) or JNK inhibitor SP600125. The results demonstrated that exposure of the cysts to plasma from CD patients resulted in enhanced paracellular permeability in a disease activity-dependent manner. Compared to HC, active CD plasma decreased ZO-1 and OCCLUDIN expression on mRNA and protein levels, and led to an increased JNK phosphorylation. Pre-incubation with adalimumab or SP600125 ameliorated TJ disruption and barrier dysfunction induced by plasma from CD patients. These results indicate that plasma from CD patients is able to induce epithelial barrier disruption, in part through TNF-α induced TJs modulation. The data also demonstrate an involvement of MAPK pathway, in particular the JNK isoform, in CD patient plasma-induced barrier dysfunction.
肠上皮屏障受多种因素影响,如肿瘤坏死因子-α(TNF-α)。克罗恩病(CD)患者的血浆 TNF-α浓度高于健康对照(HC),且与疾病活动度呈正相关。本研究旨在确定活动期和缓解期 CD 患者血浆对肠屏障功能的影响,并探讨其潜在机制。收集 CD 患者和 HC 的血浆样本。用血浆或 TNF-α处理 3D Caco-2 类器官,或用 TNF-α拮抗剂阿达木单抗(拮抗 TNF-α的单克隆抗体)或 JNK 抑制剂 SP600125 预处理。结果表明,类器官暴露于 CD 患者的血浆中,可导致细胞旁通透性以疾病活动度依赖的方式增强。与 HC 相比,活动期 CD 患者的血浆降低了 ZO-1 和 OCCLUDIN 在 mRNA 和蛋白水平的表达,并导致 JNK 磷酸化增加。用阿达木单抗或 SP600125 预处理可改善由 CD 患者血浆引起的 TJ 破坏和屏障功能障碍。这些结果表明,CD 患者的血浆能够诱导上皮屏障破坏,部分是通过 TNF-α诱导的 TJ 调节。数据还表明 MAPK 途径(特别是 JNK 同工型)参与了 CD 患者血浆诱导的屏障功能障碍。