Group I PAKs function downstream of Rac to promote podosome invasion during myoblast fusion in vivo
نویسندگان
چکیده
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.
منابع مشابه
PAKs function downstream of Rac to promote podosome invasion during myoblast fusion in vivo
The Rockefeller University Press $30.00 J. Cell Biol. Vol. 199 No. 1 169–185 www.jcb.org/cgi/doi/10.1083/jcb.201204065 JCB 169 R. Duan and P. Jin contributed equally to this paper. Correspondence to Elizabeth H. Chen: [email protected] Abbreviations used in this paper: AID, auto-inhibitory domain; DPak, Drosophila p21-activated kinase; Duf, Dumbfounded; Eve, Even skipped; FCM, fusioncompetent myob...
متن کاملAn invasive podosome-like structure promotes fusion pore formation during myoblast fusion
Recent studies in Drosophila have implicated actin cytoskeletal remodeling in myoblast fusion, but the cellular mechanisms underlying this process remain poorly understood. Here we show that actin polymerization occurs in an asymmetric and cell type-specific manner between a muscle founder cell and a fusion-competent myoblast (FCM). In the FCM, a dense F-actin-enriched focus forms at the site o...
متن کاملMuscle Differentiation: Signalling Cell Fusion
Myoblast fusion is fundamental both to the production of skeletal muscle during development and to its repair later in life. An in-depth knowledge of cell fusion in general, and myoblast fusion in particular, may also become crucial to developing clinical approaches to tissue repair based on stem cells and/or gene therapy [1,2]. But despite its importance, much remains to be learnt about cell f...
متن کاملCompetition between Blown fuse and WASP for WIP binding regulates the dynamics of WASP-dependent actin polymerization in vivo.
Dynamic rearrangements of the actin cytoskeleton play a key role in numerous cellular processes. In Drosophila, fusion between a muscle founder cell and a fusion competent myoblast (FCM) is mediated by an invasive, F-actin-enriched podosome-like structure (PLS). Here, we show that the dynamics of the PLS is controlled by Blown fuse (Blow), a cytoplasmic protein required for myoblast fusion but ...
متن کاملThe atypical Rac activator Dock180 (Dock1) regulates myoblast fusion in vivo.
Dock1 (also known as Dock180) is a prototypical member of a new family of atypical Rho GTPase activators. Genetic studies in Drosophila and Caenorhabditis elegans have demonstrated that Dock1 orthologues in these organisms have a crucial role in activating Rac GTPase signaling. We generated mutant alleles of the closely related Dock1 and Dock5 genes to study their function in mammals. We report...
متن کامل