Division of Molecular Cell Biology, Institute for Molecular Bioscience, School of Biomedical Sciences, The University of Queensland, St Lucia, Brisbane, Queensland 4072, Australia.
Nat Cell Biol. 2011 Jul 24;13(8):934-43. doi: 10.1038/ncb2290.
N-WASP is a major cytoskeletal regulator that stimulates Arp2/3-mediated actin nucleation. Here, we identify a nucleation-independent pathway by which N-WASP regulates the cytoskeleton and junctional integrity at the epithelial zonula adherens. N-WASP is a junctional protein whose depletion decreased junctional F-actin content and organization. However, N-WASP (also known as WASL) RNAi did not affect junctional actin nucleation, dominantly mediated by Arp2/3. Furthermore, the junctional effect of N-WASP RNAi was rescued by an N-WASP mutant that cannot directly activate Arp2/3. Instead, N-WASP stabilized newly formed actin filaments and facilitated their incorporation into apical rings at the zonula adherens. A major physiological effect of N-WASP at the zonula adherens thus occurs through a non-canonical pathway that is distinct from its capacity to activate Arp2/3. Indeed, the junctional impact of N-WASP was mediated by the WIP-family protein, WIRE, which binds to the N-WASP WH1 domain. We conclude that N-WASP-WIRE serves as an integrator that couples actin nucleation with the subsequent steps of filament stabilization and organization necessary for zonula adherens integrity.
N-WASP 是一种主要的细胞骨架调节因子,能刺激 Arp2/3 介导的肌动蛋白成核。在这里,我们确定了一种成核非依赖性途径,通过该途径,N-WASP 调节上皮细胞黏附连接的细胞骨架和连接完整性。N-WASP 是一种连接蛋白,其缺失会减少连接的 F-肌动蛋白含量和组织。然而,N-WASP(也称为 WASL)RNAi 不影响由 Arp2/3 主要介导的连接肌动蛋白成核。此外,N-WASP RNAi 的连接效应可以通过不能直接激活 Arp2/3 的 N-WASP 突变体来挽救。相反,N-WASP 稳定新形成的肌动蛋白丝,并促进它们整合到黏附连接的顶端环中。因此,N-WASP 在黏附连接的主要生理效应是通过一种非典型途径发生的,与它激活 Arp2/3 的能力不同。事实上,N-WASP 的连接影响是由 WIP 家族蛋白 WIRE 介导的,它与 N-WASP WH1 结构域结合。我们得出结论,N-WASP-WIRE 作为一种整合因子,将肌动蛋白成核与随后的纤维稳定和组织步骤结合起来,这对于黏附连接的完整性是必要的。