Key result
The motor function of the two-headed form of myosin-X, rather than its cargo function, is critical for actin reorganization at the leading edge and initiating filopodia formation in living cells.
The motor function of the two-headed form of myosin-X is critical for actin reorganization and initiating filopodia formation at the cell periphery.
May guide cardiovascular cell motility research; leaves open myosin-X motor targeting in human vascular models.
Filopodia are actin-rich fingerlike protrusions found at the leading edge of migrating cells and are believed to play a role in directional sensing. Previous studies have shown that myosin-X (myoX) promotes filopodia formation and that this is mediated through its ability to deliver specific cargoes to the cell periphery (Tokuo, H., and M. Ikebe. 2004. Biochem Biophys. Commun. 319:214–220; Zhang, H., J.S. Berg, Z. Li, Y. Wang, P. Lang, A.D. Sousa, A. Bhaskar, R.E. Cheney, and S. Stromblad. 2004. Nat. Cell Biol. 6:523–531; Bohil, A.B., B.W. Robertson, and R.E. Cheney. 2006. Proc. Natl. Acad. Sci. USA. 103:12411–12416; Zhu, X.J., C.Z. Wang, P.G. Dai, Y. Xie, N.N. Song, Y. Liu, Q.S. Du, L. Mei, Y.Q. Ding, and W.C. Xiong. 2007. Nat. Cell Biol. 9:184–192). In this study, we show that the motor function of myoX and not the cargo function is critical for initiating filopodia formation. Using a dimer-inducing technique, we find that myoX lacking its cargo-binding tail moves laterally at the leading edge of lamellipodia and induces filopodia in living cells. We conclude that the motor function of the two-headed form of myoX is critical for actin reorganization at the leading edge, leading to filopodia formation.
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Tokuo et al. (2007) studied Filopodia formation. Dimer-inducing technique for myoX lacking cargo-binding tail was evaluated on Filopodia formation and actin reorganization. The motor function of the two-headed form of myosin-X, rather than its cargo function, is critical for actin reorganization at the leading edge and initiating filopodia formation in living cells.
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