Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
J Cell Biol. 2012 Oct 1;199(1):169-85. doi: 10.1083/jcb.201204065. Epub 2012 Sep 24.
The p21-activated kinases (PAKs) play essential roles in diverse cellular processes and are required for cell proliferation, apoptosis, polarity establishment, migration, and cell shape changes. Here, we have identified a novel function for the group I PAKs in cell-cell fusion. We show that the two Drosophila group I PAKs, DPak3 and DPak1, have partially redundant functions in myoblast fusion in vivo, with DPak3 playing a major role. DPak3 is enriched at the site of fusion colocalizing with the F-actin focus within a podosome-like structure (PLS), and promotes actin filament assembly during PLS invasion. Although the small GTPase Rac is involved in DPak3 activation and recruitment to the PLS, the kinase activity of DPak3 is required for effective PLS invasion. We propose a model whereby group I PAKs act downstream of Rac to organize the actin filaments within the PLS into a dense focus, which in turn promotes PLS invasion and fusion pore initiation during myoblast fusion.
p21 激活激酶 (PAKs) 在多种细胞过程中发挥重要作用,是细胞增殖、凋亡、极性建立、迁移和细胞形状变化所必需的。在这里,我们发现了 I 组 PAK 在细胞融合中的一个新功能。我们表明,两种果蝇 I 组 PAK,DPak3 和 DPak1,在体内肌母细胞融合中具有部分冗余的功能,其中 DPak3 起主要作用。DPak3 在融合部位富集,与 podosome 样结构 (PLS) 内的 F-肌动蛋白焦点共定位,并在 PLS 入侵过程中促进肌动蛋白丝组装。尽管小分子 GTPase Rac 参与 DPak3 的激活和募集到 PLS,但 DPak3 的激酶活性对于有效的 PLS 入侵是必需的。我们提出了一个模型,即 I 组 PAK 作为 Rac 的下游因子,将 PLS 内的肌动蛋白丝组织成一个密集的焦点,从而促进肌母细胞融合过程中 PLS 的入侵和融合孔的启动。