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First published online 1 September 2009
doi: 10.1242/jcs.053157

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Moesin orchestrates cortical polarity of melanoma tumour cells to initiate 3D invasion

Ana Estecha¹, Lorena Sánchez-Martín¹, Amaya Puig-Kröger¹, Rubén A. Bartolomé², Joaquín Teixidó², Rafael Samaniego^3,* and Paloma Sánchez-Mateos^1,3,*,

¹ Laboratorio de Inmuno-oncología, Hospital General Universitario Gregorio Marañón, 28007 Madrid, Spain
³ Unidad de Microscopía Confocal, Hospital General Universitario Gregorio Marañón, 28007 Madrid, Spain
² Department of Cellular and Molecular Physiopathology, Centro de Investigaciones Biológicas, 28040 Madrid, Spain

Author for correspondence (rsanchezma.hgugm{at}salud.madrid.org)

Accepted 14 July 2009

Tumour cell dissemination through corporal fluids (blood, lymph and body cavity fluids) is a distinctive feature of the metastatic process. Tumour cell transition from fluid to adhesive conditions involves an early polarization event and major rearrangements of the submembrane cytoskeleton that remain poorly understood. As regulation of cortical actin-membrane binding might be important in this process, we investigated the role of ezrin and moesin, which are key crosslinking proteins of the ERM (ezrin, radixin, moesin) family. We used short interfering RNA (siRNA) to show that moesin is crucial for invasion by melanoma cells in 3D matrices and in early lung colonization. Using live imaging, we show that following initial adhesion to the endothelium or 3D matrices, moesin is redistributed away from the region of adhesion, thereby generating a polarized cortex: a stable cortical actin dome enriched in moesin and an invasive membrane domain full of blebs. Using Lifeact-GFP, a 17-amino-acid peptide that binds F-actin, we show the initial symmetry breaking of cortical actin cytoskeleton during early attachment of round cells. We also demonstrated that ezrin and moesin are differentially distributed during initial invasion of 3D matrices, and, specifically, that moesin controls adhesion-dependent activation of Rho and subsequent myosin II contractility. Our results reveal that polarized moesin plays a role in orienting Rho activation, myosin II contractility, and cortical actin stability, which is crucial for driving directional vertical migration instead of superficial spreading on the fluid-to-solid tissue interface. We propose that this mechanism of cortical polarization could sustain extravasation of fluid-borne tumour cells during the process of metastasis.

Key words: Invasion, Metastasis, Moesin, Polarity

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