Yang Cheng-Long, Yang Meng, Wang Yu-Feng, Song Chen-Cheng, DU Guan-Huan, Tang Guo-Yao
School of Stomatology, Weifang Medical University. Weifang 261021, Shandong Province, China. E-mail:
Shanghai Kou Qiang Yi Xue. 2023 Apr;32(2):126-131.
To investigate the effect of outer membrane vesicles (OMVs) secreted by Fusobacterium nucleatum (F.n) on Claudin-4 of human oral keratinocytes (HOK) and oral epithelial barrier function.
Fusobacterium nucleatum was cultured under anaerobic conditions. The OMVs were extracted by dialysis and characterized by nanosight and transmission electron microscopy (TEM). HOK were stimulated with OMVs at different mass concentrations(0-100 μg/mL) for 12 h, and stimulated with 100 μg/mL OMVs for 6 h and 12 h respectively. The expression of Claudin-4 at gene and protein level was analyzed by RT-qPCR and Western blotting. Inverted fluorescence microscope was used to observe co-localization of HOK and OMVs and localization and distribution of Claudin-4 protein. Human oral epithelial barrier was constructed by Transwell apical chamber. Transepithelial electrical resistance(TER) of barrier was measured with a transmembrane resistance measuring instrument(EVOM2), and the permeability of the barrier was evaluated by transmittance of fluorescein isothiocyanate-dextran(FD-4). Statistical analysis was performed with GraphPad Prism 8.0 software package.
Compared with the control group, the expression of Claudin-4 at protein and gene level in the HOK of OMVs stimulated group was significantly reduced (P<0.05), and immunofluorescence showed that the continuity of Claudin-4 fluorescence among cells was destroyed. OMVs stimulation decreased TER value of oral epithelial barrier(P<0.05) and increased the transmittance of FD-4(P<0.05).
OMVs derived from Fusobacterium nucleatum may damage oral mucosal epithelial barrier function through inhibiting the expression of Claudin-4.
探讨具核梭杆菌(F.n)分泌的外膜囊泡(OMVs)对人口腔角质形成细胞(HOK)紧密连接蛋白4(Claudin-4)及口腔上皮屏障功能的影响。
将具核梭杆菌在厌氧条件下培养。通过透析提取OMVs,并采用纳米可视技术和透射电子显微镜(TEM)对其进行表征。用不同质量浓度(0-100μg/mL)的OMVs刺激HOK 12小时,以及分别用100μg/mL的OMVs刺激HOK 6小时和12小时。通过RT-qPCR和蛋白质免疫印迹法分析Claudin-4在基因和蛋白水平的表达。利用倒置荧光显微镜观察HOK与OMVs的共定位以及Claudin-4蛋白的定位和分布。采用Transwell顶侧小室构建人口腔上皮屏障。用跨膜电阻测量仪(EVOM2)测量屏障的跨上皮电阻(TER),并通过异硫氰酸荧光素-葡聚糖(FD-4)的透过率评估屏障的通透性。使用GraphPad Prism 8.0软件包进行统计分析。
与对照组相比,OMVs刺激组HOK中Claudin-4在蛋白和基因水平的表达均显著降低(P<0.05),免疫荧光显示细胞间Claudin-4荧光的连续性被破坏。OMVs刺激降低了口腔上皮屏障的TER值(P<0.05),并增加了FD-4的透过率(P<0.05)。
具核梭杆菌来源的OMVs可能通过抑制Claudin-4的表达来破坏口腔黏膜上皮屏障功能。