Actin dynamics sustains spatial gradients of membrane tension in adherent cells

bioRxiv Pub Date : 2024-07-16 DOI:10.1101/2024.07.15.603517
J. M. García-Arcos, Amine Mehidi, Julissa Sánchez Velázquez, Pau Guillamat, C. Tomba, Laura Houzet, L. Capolupo, Giovanni D’Angelo, Adai Colom, Elizabeth Hinde, Charlotte Aumeier, Aurélien Roux
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Abstract

Tension propagates extremely fast in lipid bilayers, precluding the formation of tension gradients. Nevertheless, plasma membrane tension gradients have been evidenced in migrating cells and along axons. Here, using a fluorescent membrane tension probe, we show that membrane tension gradients exist in all adherent cells, whether they migrate or not. Non-adhering cells do not display tension gradients. We further show that branched actin increases tension, while membrane-to-cortex attachments facilitate its propagation. Tension is the lowest at the edge of adhesion sites and highest at protrusions, setting the boundaries of the tension gradients. By providing a quantitative and mechanistic basis behind the organization of membrane tension gradients, our work explains how they are actively sustained in adherent cells.
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肌动蛋白动力学维持粘附细胞膜张力的空间梯度
张力在脂质双层膜中的传播速度极快,因此无法形成张力梯度。然而,在迁移细胞和轴突上已经证明了质膜张力梯度。在这里,我们使用荧光膜张力探针证明,无论细胞是否迁移,所有粘附细胞中都存在膜张力梯度。非粘附细胞不显示张力梯度。我们进一步发现,分枝肌动蛋白会增加张力,而膜与皮层的附着会促进张力的传播。粘附点边缘的张力最低,突起处的张力最高,从而确定了张力梯度的边界。通过提供膜张力梯度组织背后的定量和机理基础,我们的工作解释了如何在粘附细胞中积极维持膜张力梯度。
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