TY - JOUR
T1 - The actin regulator N-WASp is required for muscle-cell fusion in mice
AU - Gruenbaum-Cohen, Yael
AU - Harel, Itamar
AU - Umansky, Kfir Baruch
AU - Tzahor, Eldad
AU - Snapper, Scott B.
AU - Shilo, Ben Zion
AU - Schejter, Eyal D.
N1 - Israel Science Foundation (ISF); Muscular Dystrophy Association; MYORES; ISF Legacy Grant [1875/08]We thank Paul Knopp and Peter Zammit (King's College, London) for providing instruction and sharing their expertise on generation and handling of satellite cell cultures. We thank our colleagues Ari Elson, David Goldhamer, Yoram Groner, Eran Hornstein, Ronen Schweitzer, and Eli Zelzer for advice, reagents, and use of laboratory facilities; Margaret Buckingham for insightful discussions; Sagi Levy for instruction and help in quantifying myoblast motility; R'ada Massarwa, Ariel Rinon, and Natti Weinblum for their contributions to experiments performed in the course of this study; and all members of the B.-Z. S. laboratory for their help and support. This work was supported by research grants from the Israel Science Foundation (ISF) and the Muscular Dystrophy Association (to B-Z.S. and E. D. S.) and a MYORES travel grant (to Y.G-C.). K-B. U. was supported by ISF Legacy Grant 1875/08. B-Z.S. is an incumbent of the Hilda and Cecil Lewis Chair in Molecular Genetics.
PY - 2012/7/10
Y1 - 2012/7/10
N2 - A fundamental aspect of skeletal myogenesis involves extensive rounds of cell fusion, in which individualmyoblasts 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.
AB - A fundamental aspect of skeletal myogenesis involves extensive rounds of cell fusion, in which individualmyoblasts 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.
KW - Actin nucleation
KW - Myotube formation
UR - http://www.scopus.com/inward/record.url?scp=84863977654&partnerID=8YFLogxK
U2 - https://doi.org/10.1073/pnas.1116065109
DO - https://doi.org/10.1073/pnas.1116065109
M3 - مقالة
C2 - 22736793
SN - 0027-8424
VL - 109
SP - 11211
EP - 11216
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 28
ER -