Ikenouchi Junichi, Umeda Kazuaki, Tsukita Sachiko, Furuse Mikio, Tsukita Shoichiro
Department of Cell Biology, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan.
J Cell Biol. 2007 Mar 12;176(6):779-86. doi: 10.1083/jcb.200612080.
The molecular mechanisms of how primordial adherens junctions (AJs) evolve into spatially separated belt-like AJs and tight junctions (TJs) during epithelial polarization are not well understood. Previously, we reported the establishment of ZO-1/ZO-2-deficient cultured epithelial cells (1[ko]/2[kd] cells), which lacked TJs completely. In the present study, we found that the formation of belt-like AJs was significantly delayed in 1(ko)/2(kd) cells during epithelial polarization. The activation of Rac1 upon primordial AJ formation is severely impaired in 1(ko)/2(kd) cells. Our data indicate that ZO-1 plays crucial roles not only in TJ formation, but also in the conversion from "fibroblastic" AJs to belt-like "polarized epithelial" AJs through Rac1 activation. Furthermore, to examine whether ZO-1 itself mediate belt-like AJ and TJ formation, respectively, we performed a mutational analysis of ZO-1. The requirement for ZO-1 differs between belt-like AJ and TJ formation. We propose that ZO-1 is directly involved in the establishment of two distinct junctional domains, belt-like AJs and TJs, during epithelial polarization.
在上皮细胞极化过程中,原始黏附连接(AJs)如何演变为空间上分离的带状AJs和紧密连接(TJs)的分子机制尚不清楚。此前,我们报道了ZO-1/ZO-2缺陷培养上皮细胞(1[敲除]/2[敲低]细胞)的建立,这些细胞完全缺乏TJs。在本研究中,我们发现1(敲除)/2(敲低)细胞在上皮细胞极化过程中,带状AJs的形成显著延迟。在原始AJ形成时,1(敲除)/2(敲低)细胞中Rac1的激活严重受损。我们的数据表明,ZO-1不仅在TJ形成中起关键作用,而且通过激活Rac1在从“成纤维细胞样”AJs向带状“极化上皮”AJs的转变中也起关键作用。此外,为了分别研究ZO-1本身是否介导带状AJ和TJ的形成,我们对ZO-1进行了突变分析。带状AJ和TJ形成对ZO-1的需求不同。我们提出,ZO-1直接参与上皮细胞极化过程中两个不同连接域——带状AJs和TJs的建立。