Department of Oral and Maxillofacial Surgery, Peking University School and Hospital of Stomatology, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing, China.
Department of Physiology and Pathophysiology, Peking University School of Basic Medical Sciences, Key Laboratory of Molecular Cardiovascular Sciences, Ministry of Education, and Beijing Key Laboratory of Cardiovascular Receptors Research, Beijing, China.
J Dent Res. 2020 Mar;99(3):302-310. doi: 10.1177/0022034519896749. Epub 2019 Dec 20.
Volume and composition of saliva are crucial for oral and systemic health. How substances, particularly macromolecules, are transported across the salivary gland epithelium has not been established in detail. Tricellulin is a component of tricellular tight junctions that form a central tube to serve as an important route for macromolecule transport. Whether tricellulin is expressed in the submandibular gland (SMG) and involved in salivation has been unknown. Here, by using Western blotting and immunofluorescence, tricellulin was found to be characteristically localized at tricellular contacts of human, rat, and mouse SMGs. Knockdown of tricellulin significantly increased, whereas overexpression of tricellulin decreased, paracellular permeability for 40-kDa but not for 4-kDa fluorescein isothiocyanate-dextran, while transepithelial electrical resistance was unaffected. Conversely, claudin-4 knockdown and overexpression affected transepithelial electrical resistance but not 40-kDa fluorescein isothiocyanate-dextran transport, suggesting that tricellulin regulated transport of macromolecules but not ions, which were mainly regulated by bicellular tight junctions (bTJs). Moreover, tricellulin was dynamically redistributed from tri- to bicellular membranes in cholinergically stimulated SMG tissues and cells. Immunoglobulin-like domain-containing receptor 1 (ILDR1) recruits tricellulin to tricellular contacts. The proportion of macromolecules in the saliva was increased, whereas the amount of stimulated saliva was unchanged in mice, which displayed abnormal tricellulin distribution in SMGs. Furthermore, tricellulin interacted with bTJ proteins, such as occludin, claudin-1, claudin-3, claudin-4, and ZO-1, in rat SMG epithelial polarized cell line SMG-C6. Knockdown of tricellulin decreased occludin levels. Thus, we revealed a specific expression pattern of tricellulin in SMG epithelium. Tricellulin not only functioned as a barrier for macromolecules but also modulated the connection of bTJs to the tight junction complex. Alterations in tricellulin expression and distribution could thereby change salivary composition. Our study provided novel insights on salivary gland tight junction organization and function.
唾液的体积和成分对口腔和全身健康至关重要。物质,特别是大分子,是如何穿过唾液腺上皮细胞运输的,目前还没有详细的研究结果。三连接蛋白是三连接紧密连接的组成部分,形成中央管,作为大分子运输的重要途径。三连接蛋白是否在颌下腺 (SMG) 中表达并参与唾液分泌还不清楚。在这里,通过 Western blot 和免疫荧光,发现三连接蛋白在人、大鼠和小鼠 SMG 的三连接点上具有特征性定位。三连接蛋白的敲低显著增加,而过表达则显著减少,40kDa 而不是 4kDa 异硫氰酸荧光素右旋糖苷的细胞旁通透性,而细胞间电阻不受影响。相反,claudin-4 的敲低和过表达影响细胞间电阻,但不影响 40kDa 异硫氰酸荧光素右旋糖苷的转运,表明三连接蛋白调节大分子的转运,而不是离子的转运,离子的转运主要由双连接紧密连接 (bTJs) 调节。此外,三连接蛋白在胆碱能刺激的 SMG 组织和细胞中从三连接点动态重新分布到双连接点。免疫球蛋白样结构域包含受体 1 (ILDR1) 将三连接蛋白募集到三连接点。在 SMG 中显示异常三连接蛋白分布的 小鼠中,唾液中的大分子比例增加,而刺激唾液的量不变。此外,三连接蛋白与 bTJ 蛋白相互作用,如 occludin、claudin-1、claudin-3、claudin-4 和 ZO-1,在大鼠 SMG 上皮极性细胞系 SMG-C6 中。三连接蛋白的敲低降低了 occludin 的水平。因此,我们揭示了三连接蛋白在 SMG 上皮中的特定表达模式。三连接蛋白不仅作为大分子的屏障,还调节 bTJs 与紧密连接复合物的连接。三连接蛋白表达和分布的改变可能会改变唾液的组成。我们的研究为唾液腺紧密连接的组织和功能提供了新的见解。