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Staff member

Anabel-Lise Le Roux

Cellular and Molecular Mechanobiology
35342
Staff member publications

Le Roux, Anabel-Lise, Venturini, Valeria, Gómez-González, Manuel, Beedle, Amy EM., Quiroga, Xarxa, Menino, Xavier, Trepat, Xavier, Roca-Cusachs, Pere, (2025). Equibiaxial Stretching Device for High Magnification Live-Cell Confocal Fluorescence Microscopy Jove-Journal Of Visualized Experiments , e67520

Mohammad, Irrem-Laareb, Giannotti, Marina I, Fourgous, Elise, Boublik, Yvan, Fernández, Alejandro, Le Roux, Anabel-Lise, Sirvent, Audrey, Taulés, Marta, Roche, Serge, Pons, Miquel, (2025). Lipid-driven Src self-association modulates its transformation capacity Life Sci Alliance 8, e202403019

Pons, Miquel

JTD

Elosegui-Artola, A., Andreu, I., Beedle, A. E. M., Lezamiz, A., Uroz, M., Kosmalska, A. J., Oria, R., Kechagia, J. Z., Rico-Lastres, P., Le Roux, A. L., Shanahan, C. M., Trepat, X., Navajas, D., Garcia-Manyes, S., Roca-Cusachs, P., (2017). Force triggers YAP nuclear entry by regulating transport across nuclear pores Cell 171, (6), 1397-1410

YAP is a mechanosensitive transcriptional activator with a critical role in cancer, regeneration, and organ size control. Here, we show that force applied to the nucleus directly drives YAP nuclear translocation by decreasing the mechanical restriction of nuclear pores to molecular transport. Exposure to a stiff environment leads cells to establish a mechanical connection between the nucleus and the cytoskeleton, allowing forces exerted through focal adhesions to reach the nucleus. Force transmission then leads to nuclear flattening, which stretches nuclear pores, reduces their mechanical resistance to molecular transport, and increases YAP nuclear import. The restriction to transport is further regulated by the mechanical stability of the transported protein, which determines both active nuclear transport of YAP and passive transport of small proteins. Our results unveil a mechanosensing mechanism mediated directly by nuclear pores, demonstrated for YAP but with potential general applicability in transcriptional regulation. Force-dependent changes in nuclear pores control protein access to the nucleus.

JTD Keywords: Atomic force microscopy, Hippo pathway, Mechanosensing, Mechanotransduction, Molecular mechanical stability, Nuclear mechanics, Nuclear pores, Nuclear transport, Rigidity sensing, Transcription regulation

Pontes, B., Monzo, P., Gole, L., Le Roux, A. L., Kosmalska, A. J., Tam, Z. Y., Luo, W., Kan, S., Viasnoff, V., Roca-Cusachs, P., Tucker-Kellogg, L., Gauthier, N. C., (2017). Membrane tension controls adhesion positioning at the leading edge of cells Journal of Cell Biology , 216, (9), 2959-2977

Cell migration is dependent on adhesion dynamics and actin cytoskeleton remodeling at the leading edge. These events may be physically constrained by the plasma membrane. Here, we show that the mechanical signal produced by an increase in plasma membrane tension triggers the positioning of new rows of adhesions at the leading edge. During protrusion, as membrane tension increases, velocity slows, and the lamellipodium buckles upward in a myosin II-independent manner. The buckling occurs between the front of the lamellipodium, where nascent adhesions are positioned in rows, and the base of the lamellipodium, where a vinculin-dependent clutch couples actin to previously positioned adhesions. As membrane tension decreases, protrusion resumes and buckling disappears, until the next cycle. We propose that the mechanical signal of membrane tension exerts upstream control in mechanotransduction by periodically compressing and relaxing the lamellipodium, leading to the positioning of adhesions at the leading edge of cells.

JTD