An invasive podosome-like structure promotes fusion pore formation during myoblast fusion

K. Sens(Johns Hopkins University), Shiliang Zhang(Johns Hopkins University), Peng Jin(Johns Hopkins University), Rui Duan(Johns Hopkins University), Guofeng Zhang(National Institute of Biomedical Imaging and Bioengineering), Fengbao Luo(Johns Hopkins University), Lauren Parachini(Johns Hopkins University), Elizabeth H. Chen(Johns Hopkins University)
The Journal of Cell Biology
November 22, 2010
Cited by 200Open Access
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Abstract

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 of fusion, whereas a thin sheath of F-actin is induced along the apposing founder cell membrane. The FCM-specific actin focus invades the apposing founder cell with multiple finger-like protrusions, leading to the formation of a single-channel macro fusion pore between the two muscle cells. Two actin nucleation-promoting factors of the Arp2/3 complex, WASP and Scar, are required for the formation of the F-actin foci, whereas WASP but not Scar promotes efficient foci invasion. Our studies uncover a novel invasive podosome-like structure (PLS) in a developing tissue and reveal a previously unrecognized function of PLSs in facilitating cell membrane juxtaposition and fusion.


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