MRC-Laboratory of Molecular Cell Biology, UCL, London, WC1E 6BT, UK.
J Cell Sci. 2010 Apr 1;123(Pt 7):1089-98. doi: 10.1242/jcs.060772. Epub 2010 Mar 2.
Different actin-filament-based structures co-exist in many cells. Here, we characterise dynamic actin-based protrusions that form at distinct positions within columnar epithelial cells, focusing on basal filopodia and sheet-like intermediate-level protrusions that extend between surrounding epithelial cells. Using a genetic analysis, we found that the form and distribution of these actin-filament-based structures depends on the activities of apical polarity determinants, not on basal integrin signalling. Bazooka/Par3 acts upstream of the RacGEF Sif/TIAM1 to limit filopodia to the basal domain, whereas Cdc42, aPKC and Par6 are required for normal protrusion morphology and dynamics. Downstream of these polarity regulators, Sif/TIAM1, Rac, SCAR and Arp2/3 complexes catalyse actin nucleation to generate lamellipodia and filopodia, whose form depends on the level of Rac activation. Taken together, these data reveal a role for Baz/Par3 in the establishment of an intercellular gradient of Rac inhibition, from apical to basal, and an intimate association between different apically concentrated Par proteins and Rho-family GTPases in the regulation of the distribution and structure of the polarised epithelial actin cytoskeleton.
在许多细胞中,不同的肌动蛋白丝基结构共存。在这里,我们描述了在柱状上皮细胞内的不同位置形成的动态肌动蛋白丝基突起,重点关注基底丝状伪足和在周围上皮细胞之间延伸的片状中间水平突起。通过遗传分析,我们发现这些肌动蛋白丝基结构的形式和分布取决于顶端极性决定因素的活性,而不是基底整联蛋白信号。Bazooka/Par3 在上游作用于 RacGEF Sif/TIAM1,将丝状伪足限制在基底区域,而 Cdc42、aPKC 和 Par6 是正常突起形态和动力学所必需的。在这些极性调节剂的下游,Sif/TIAM1、Rac、SCAR 和 Arp2/3 复合物催化肌动蛋白成核,产生片状伪足和丝状伪足,其形式取决于 Rac 激活的水平。总之,这些数据揭示了 Baz/Par3 在建立从顶端到基底的 Rac 抑制的细胞间梯度以及不同顶端集中的 Par 蛋白和 Rho 家族 GTPases 在调节极化上皮肌动蛋白细胞骨架的分布和结构中的密切关联中的作用。