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The actin regulator N-WASp is required for muscle-cell fusion in mice.


ABSTRACT: A fundamental aspect of skeletal myogenesis involves extensive rounds of cell fusion, in which individual myoblasts are incorporated into growing muscle fibers. Here we demonstrate that N-WASp, a ubiquitous nucleation-promoting factor of branched microfilament arrays, is an essential contributor to skeletal muscle-cell fusion in developing mouse embryos. Analysis both in vivo and in primary satellite-cell cultures, shows that disruption of N-WASp function does not interfere with the program of skeletal myogenic differentiation, and does not affect myoblast motility, morphogenesis and attachment capacity. N-WASp-deficient myoblasts, however, fail to fuse. Furthermore, our analysis suggests that myoblast fusion requires N-WASp activity in both partners of a fusing myoblast pair. These findings reveal a specific role for N-WASp during mammalian myogenesis. WASp-family elements appear therefore to act as universal mediators of the myogenic cell-cell fusion mechanism underlying formation of functional muscle fibers, in both vertebrate and invertebrate species.

SUBMITTER: Gruenbaum-Cohen Y 

PROVIDER: S-EPMC3396508 | biostudies-literature | 2012 Jul

REPOSITORIES: biostudies-literature

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The actin regulator N-WASp is required for muscle-cell fusion in mice.

Gruenbaum-Cohen Yael Y   Harel Itamar I   Umansky Kfir-Baruch KB   Tzahor Eldad E   Snapper Scott B SB   Shilo Ben-Zion BZ   Schejter Eyal D ED  

Proceedings of the National Academy of Sciences of the United States of America 20120626 28


A fundamental aspect of skeletal myogenesis involves extensive rounds of cell fusion, in which individual myoblasts are incorporated into growing muscle fibers. Here we demonstrate that N-WASp, a ubiquitous nucleation-promoting factor of branched microfilament arrays, is an essential contributor to skeletal muscle-cell fusion in developing mouse embryos. Analysis both in vivo and in primary satellite-cell cultures, shows that disruption of N-WASp function does not interfere with the program of s  ...[more]

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