UNIROUEN, INSERM U1245, Normandy Centre for Genomic and Personalized Medicine, Normandie University, Rouen, France.
Laboratory of Mucosal Barrier Pathobiology, Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Nat Rev Gastroenterol Hepatol. 2023 Jul;20(7):417-432. doi: 10.1038/s41575-023-00766-3. Epub 2023 Apr 25.
Epithelial tight junctions define the paracellular permeability of the intestinal barrier. Molecules can cross the tight junctions via two distinct size-selective and charge-selective paracellular pathways: the pore pathway and the leak pathway. These can be distinguished by their selectivities and differential regulation by immune cells. However, permeability increases measured in most studies are secondary to epithelial damage, which allows non-selective flux via the unrestricted pathway. Restoration of increased unrestricted pathway permeability requires mucosal healing. By contrast, tight junction barrier loss can be reversed by targeted interventions. Specific approaches are needed to restore pore pathway or leak pathway permeability increases. Recent studies have used preclinical disease models to demonstrate the potential of pore pathway or leak pathway barrier restoration in disease. In this Review, we focus on the two paracellular flux pathways that are dependent on the tight junction. We discuss the latest evidence that highlights tight junction components, structures and regulatory mechanisms, their impact on gut health and disease, and opportunities for therapeutic intervention.
上皮细胞紧密连接定义了肠道屏障的细胞旁通透性。分子可以通过两种不同的大小选择性和电荷选择性细胞旁途径穿过紧密连接:孔道途径和渗漏途径。可以通过它们的选择性和免疫细胞的差异调节来区分它们。然而,大多数研究中测量的通透性增加是上皮损伤的继发结果,这允许通过无限制途径进行非选择性通量。增加的无限制途径通透性的恢复需要黏膜愈合。相比之下,通过靶向干预可以逆转紧密连接屏障的损失。需要特定的方法来恢复孔道途径或渗漏途径通透性的增加。最近的研究使用临床前疾病模型证明了在疾病中恢复孔道或渗漏途径屏障通透性的潜力。在这篇综述中,我们重点介绍了依赖于紧密连接的两种细胞旁通量途径。我们讨论了最新的证据,强调了紧密连接的组成部分、结构和调节机制,它们对肠道健康和疾病的影响,以及治疗干预的机会。