Laboratory of Bioimaging and Cell Signaling, Graduate School of Biostudies, Kyoto University, Yoshida Konoe-cho, Kyoto 606-8501, Japan.
EMBO Rep. 2012 Mar 1;13(3):237-43. doi: 10.1038/embor.2011.249.
Using MDCK cells that constitutively express a Förster resonance energy transfer biosensor, we found that Rac1 activity is homogenous at the entire plasma membrane in early stages of cystogenesis, whereas in later stages Rac1 activity is higher at the lateral membrane than at the apical plasma membrane. If Rac1 is activated at the apical membrane in later stages, however, the monolayer cells move into the luminal space. In these cells, tight junctions are disrupted, accompanied by mislocalization of polarization markers and disorientation of cell division. These observations indicate that Rac1 suppression at the apical membrane is essential for the maintenance of cyst structure.
使用组成型表达Förster 共振能量转移生物传感器的 MDCK 细胞,我们发现 Rac1 活性在囊泡形成的早期阶段在整个质膜上是均匀的,而在后期阶段 Rac1 活性在侧膜上高于顶质膜。然而,如果 Rac1 在后期阶段在顶质膜上被激活,那么单层细胞会移动到腔隙空间。在这些细胞中,紧密连接被破坏,伴随着极化标记物的定位错误和细胞分裂的定向紊乱。这些观察结果表明 Rac1 在顶质膜上的抑制对于维持囊泡结构是必不可少的。