Hutterer Andrea, Betschinger Joerg, Petronczki Mark, Knoblich Juergen A
Research Institute of Molecular Pathology, Dr. Bohr Gasse 7, 1030 Vienna, Austria.
Dev Cell. 2004 Jun;6(6):845-54. doi: 10.1016/j.devcel.2004.05.003.
How epithelial cells subdivide their plasma membrane into an apical and a basolateral domain is largely unclear. In Drosophila embryos, epithelial cells are generated from a syncytium during cellularization. We show here that polarity is established shortly after cellularization when Par-6 and the atypical protein kinase C concentrate on the apical side of the newly formed cells. Apical localization of Par-6 requires its interaction with activated Cdc42 and dominant-active or dominant-negative Cdc42 disrupt epithelial polarity, suggesting that activation of this GTPase is crucial for the establishment of epithelial polarity. Maintenance of Par-6 localization requires the cytoskeletal protein Lgl. Genetic and biochemical experiments suggest that phosphorylation by aPKC inactivates Lgl on the apical side. On the basolateral side, Lgl is active and excludes Par-6 from the cell cortex, suggesting that complementary cortical domains are maintained by mutual inhibition of aPKC and Lgl on opposite sides of an epithelial cell.
上皮细胞如何将其质膜划分为顶端和基底外侧结构域在很大程度上尚不清楚。在果蝇胚胎中,上皮细胞是在细胞化过程中由合胞体产生的。我们在此表明,极性在细胞化后不久就得以建立,此时Par-6和非典型蛋白激酶C集中在新形成细胞的顶端。Par-6的顶端定位需要它与活化的Cdc42相互作用,并且显性激活或显性阴性的Cdc42会破坏上皮极性,这表明这种GTP酶的激活对于上皮极性的建立至关重要。Par-6定位的维持需要细胞骨架蛋白Lgl。遗传和生化实验表明,aPKC的磷酸化使顶端的Lgl失活。在基底外侧,Lgl是有活性的,并将Par-6排除在细胞皮质之外,这表明上皮细胞相对两侧的aPKC和Lgl相互抑制维持了互补的皮质结构域。