Inoko Akihito, Itoh Masahiko, Tamura Atsushi, Matsuda Miho, Furuse Mikio, Tsukita Shoichiro
Department of Cell Biology, Faculty of Medicine, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan.
Genes Cells. 2003 Nov;8(11):837-45. doi: 10.1046/j.1365-2443.2003.00681.x.
Three related MAGUK proteins, ZO-1, ZO-2 and ZO-3, are concentrated at the cytoplasmic surface of tight junctions. However, in contrast to ZO-1/ZO-2, our knowledge of the expression and distribution of ZO-3 is still fragmentary, partly due to a lack of antibodies that specifically distinguish ZO-3 from ZO-1 and ZO-2.
We generated one pAb and one mAb that specifically recognized ZO-3 on Western blotting. The immunofluorescence signals obtained with these antibodies completely disappeared from ZO-1/ZO-2-positive tight junctions in the liver of ZO-3-deficient mice, indicating that the antibodies can be used to localize ZO-3 in various tissues by immunofluorescence microscopy. Immunofluorescence microscopy with these antibodies revealed that ZO-3 was concentrated at tight junctions in various types of epithelium, but not in endothelium or at cadherin-based cell-cell adhesion sites (spot adherens junctions of fibroblasts and intercalated discs of cardiac muscle cells), where ZO-1 and ZO-2 are concentrated.
We conclude that ZO-3 is expressed in a more epithelium-specific manner than ZO-1 and ZO-2. These observations provide for a better understanding of the functions of tight junction-associated MAGUKs.
三种相关的膜相关鸟苷酸激酶(MAGUK)蛋白,即紧密连接蛋白1(ZO-1)、紧密连接蛋白2(ZO-2)和紧密连接蛋白3(ZO-3),集中在紧密连接的细胞质表面。然而,与ZO-1/ZO-2不同,我们对ZO-3表达和分布的了解仍然不完整,部分原因是缺乏能将ZO-3与ZO-1和ZO-2特异性区分开的抗体。
我们制备了一种在蛋白质免疫印迹法中能特异性识别ZO-3的多克隆抗体(pAb)和一种单克隆抗体(mAb)。用这些抗体获得的免疫荧光信号在ZO-3缺陷小鼠肝脏中ZO-1/ZO-2阳性的紧密连接处完全消失,这表明这些抗体可用于通过免疫荧光显微镜在各种组织中定位ZO-3。用这些抗体进行免疫荧光显微镜观察发现,ZO-3集中在各种上皮细胞的紧密连接处,但在内皮细胞或基于钙黏蛋白的细胞-细胞黏附位点(成纤维细胞的点状黏附连接和心肌细胞的闰盘)中不集中,而ZO-1和ZO-2集中在这些位点。
我们得出结论,ZO-3的表达比ZO-1和ZO-2更具上皮细胞特异性。这些观察结果有助于更好地理解紧密连接相关MAGUKs的功能。