Nambiar Rajalakshmi, McConnell Russell E, Tyska Matthew J
Department of Cell and Developmental Biology, Vanderbilt University Medical Center, Nashville, TN 37205, USA.
Proc Natl Acad Sci U S A. 2009 Jul 21;106(29):11972-7. doi: 10.1073/pnas.0901641106. Epub 2009 Jul 2.
All cell functions that involve membrane deformation or a change in cell shape (e.g., endocytosis, exocytosis, cell motility, and cytokinesis) are regulated by membrane tension. While molecular contacts between the plasma membrane and the underlying actin cytoskeleton are known to make significant contributions to membrane tension, little is known about the molecules that mediate these interactions. We used an optical trap to directly probe the molecular determinants of membrane tension in isolated organelles and in living cells. Here, we show that class I myosins, a family of membrane-binding, actin-based motor proteins, mediate membrane/cytoskeleton adhesion and thus, make major contributions to membrane tension. These studies show that class I myosins directly control the mechanical properties of the cell membrane; they also position these motor proteins as master regulators of cellular events involving membrane deformation.
所有涉及膜变形或细胞形状变化的细胞功能(如内吞作用、外排作用、细胞运动和胞质分裂)均受膜张力调控。虽然已知质膜与下方的肌动蛋白细胞骨架之间的分子接触对膜张力有重大贡献,但对于介导这些相互作用的分子却知之甚少。我们使用光镊直接探测分离细胞器和活细胞中膜张力的分子决定因素。在此,我们表明I类肌球蛋白(一类基于肌动蛋白的膜结合运动蛋白家族)介导膜/细胞骨架黏附,因此对膜张力有重大贡献。这些研究表明,I类肌球蛋白直接控制细胞膜的力学特性;它们还将这些运动蛋白定位为涉及膜变形的细胞事件的主要调节因子。