Donato Rino P, El-Merhibi Adaweyah, Gundsambuu Batjargal, Mak Kai Yan, Formosa Emma R, Wang Xian, Abbott Catherine A, Powell Barry C
Women's and Children's Health Research Institute, North Adelaide, SA, Australia.
Methods Mol Biol. 2011;763:115-37. doi: 10.1007/978-1-61779-191-8_8.
The integrity, or barrier function, of the intestinal epithelium is of paramount importance in -maintaining good health. This is largely imparted by a single layer of epithelial cells linked by the transmembrane tight junction protein complex near their apical surface. Disruption of epithelial permeability via the tight junctions can contribute to disease progression. The cytokine IFNγ is involved in many inflammatory processes and has been shown to dramatically increase permeability via changes at the tight junction in experimental models. One of its key effectors is the transcription factor, -IRF-1. In our studies of the role of IRF-1 in barrier function using the human T84 intestinal epithelial cell monolayer model, we have found that induction of IRF-1 alone is insufficient to change permeability and that if IRF-1 is involved in mediating the permeability effects of IFNγ, then other factors must also be required.
肠道上皮的完整性或屏障功能对于维持良好健康至关重要。这在很大程度上是由单层上皮细胞在其顶端表面附近通过跨膜紧密连接蛋白复合体连接而赋予的。通过紧密连接破坏上皮通透性会促进疾病进展。细胞因子IFNγ参与许多炎症过程,并且在实验模型中已显示通过紧密连接处的变化显著增加通透性。其关键效应器之一是转录因子IRF-1。在我们使用人T84肠道上皮细胞单层模型研究IRF-1在屏障功能中的作用时,我们发现单独诱导IRF-1不足以改变通透性,并且如果IRF-1参与介导IFNγ的通透性效应,那么还必须有其他因素。