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7H6抗原在紧密连接处的定位与MDCK细胞的细胞旁屏障功能相关。

Localization of the 7H6 antigen at tight junctions correlates with the paracellular barrier function of MDCK cells.

作者信息

Zhong Y, Enomoto K, Isomura H, Sawada N, Minase T, Oyamada M, Konishi Y, Mori M

机构信息

Department of Pathology, Sapporo Medical University School of Medicine, Japan.

出版信息

Exp Cell Res. 1994 Oct;214(2):614-20. doi: 10.1006/excr.1994.1299.

Abstract

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.

摘要

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。

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