Zhong Y, Enomoto K, Isomura H, Sawada N, Minase T, Oyamada M, Konishi Y, Mori M
Department of Pathology, Sapporo Medical University School of Medicine, Japan.
Exp Cell Res. 1994 Oct;214(2):614-20. doi: 10.1006/excr.1994.1299.
An important function of the tight junction is to act as a selective barrier to ions and small molecules, although no molecule responsible for the barrier function has been identified. Here we report evidence that the localization of the 7H6 tight junction-associated antigen identified in our laboratory at tight junctions correlates with the barrier function of MDCK cells. MDCK cells in a confluent monolayer possessed a polarized morphology, having an apical plasma membrane and a basolateral membrane, which is separated from the former by tight junctions. MDCK cells expressed both ZO-1 and 7H6 antigen at tight junctions, which maintain a tight barrier as determined by resistance to lanthanum permeation and high transepithelial electrical resistance (TER, 1500 ohm-cm2). The 7H6 antigen disappeared as tight junctions became permeable to lanthanum with a decrease in TER (below 100 ohm-cm2) due to treatment with metabolic inhibitors (10 microns antimycin A and 10 mM 2-deoxyglucose) for 30 min, while leaving ZO-1 at the cell border. The 7H6 antigen appeared at tight junctions again as TER recovered to a high level (1500 ohm-cm2) within 3 h after withdrawal of metabolic inhibitors. In addition, we found that 7H6 antigen is a phosphorylated protein and that phosphorylation is closely related to the localization of 7H6 antigen in the area of tight junctions.
紧密连接的一个重要功能是作为对离子和小分子的选择性屏障,尽管尚未鉴定出负责该屏障功能的分子。在此我们报告证据表明,我们实验室鉴定的7H6紧密连接相关抗原在紧密连接处的定位与MDCK细胞的屏障功能相关。汇合单层中的MDCK细胞具有极化形态,具有顶端质膜和基底外侧膜,它们由紧密连接与前者分隔开。MDCK细胞在紧密连接处同时表达ZO-1和7H6抗原,通过对镧渗透的抗性和高跨上皮电阻(TER,1500欧姆·厘米²)确定其维持紧密屏障。由于用代谢抑制剂(10微摩尔抗霉素A和10毫摩尔2-脱氧葡萄糖)处理30分钟,随着紧密连接对镧变得通透且TER降低(低于100欧姆·厘米²),7H6抗原消失,而ZO-1留在细胞边界。在撤除代谢抑制剂后3小时内,随着TER恢复到高水平(1500欧姆·厘米²),7H6抗原再次出现在紧密连接处。此外,我们发现7H6抗原是一种磷酸化蛋白,并且磷酸化与7H6抗原在紧密连接区域的定位密切相关。