Stachowiak Matthew R, Smith Mark A, Blankman Elizabeth, Chapin Laura M, Balcioglu Hayri E, Wang Shuyuan, Beckerle Mary C, O'Shaughnessy Ben
Departments of Chemical Engineering.
Departments of Biology and Oncological Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112.
Proc Natl Acad Sci U S A. 2014 Dec 9;111(49):17528-33. doi: 10.1073/pnas.1417686111. Epub 2014 Nov 24.
Cytoskeletal actin assemblies transmit mechanical stresses that molecular sensors transduce into biochemical signals to trigger cytoskeletal remodeling and other downstream events. How mechanical and biochemical signaling cooperate to orchestrate complex remodeling tasks has not been elucidated. Here, we studied remodeling of contractile actomyosin stress fibers. When fibers spontaneously fractured, they recoiled and disassembled actin synchronously. The disassembly rate was accelerated more than twofold above the resting value, but only when contraction increased the actin density to a threshold value following a time delay. A mathematical model explained this as originating in the increased overlap of actin filaments produced by myosin II-driven contraction. Above a threshold overlap, this mechanical signal is transduced into accelerated disassembly by a mechanism that may sense overlap directly or through associated elastic stresses. This biochemical response lowers the actin density, overlap, and stresses. The model showed that this feedback mechanism, together with rapid stress transmission along the actin bundle, spatiotemporally synchronizes actin disassembly and fiber contraction. Similar actin remodeling kinetics occurred in expanding or contracting intact stress fibers but over much longer timescales. The model accurately described these kinetics, with an almost identical value of the threshold overlap that accelerates disassembly. Finally, we measured resting stress fibers, for which the model predicts constant actin overlap that balances disassembly and assembly. The overlap was indeed regulated, with a value close to that predicted. Our results suggest that coordinated mechanical and biochemical signaling enables extended actomyosin assemblies to adapt dynamically to the mechanical stresses they convey and direct their own remodeling.
细胞骨架肌动蛋白组装体传递机械应力,分子传感器将其转化为生化信号,以触发细胞骨架重塑和其他下游事件。机械信号和生化信号如何协同作用来协调复杂的重塑任务尚未阐明。在这里,我们研究了收缩性肌动球蛋白应力纤维的重塑。当纤维自发断裂时,它们会回弹并同步拆解肌动蛋白。拆解速率比静止值加快了两倍多,但只有在收缩使肌动蛋白密度在延迟后增加到阈值时才会如此。一个数学模型解释说,这源于肌球蛋白II驱动的收缩所产生的肌动蛋白丝重叠增加。超过阈值重叠时,这个机械信号通过一种可能直接感知重叠或通过相关弹性应力来转导为加速拆解。这种生化反应降低了肌动蛋白密度、重叠和应力。该模型表明,这种反馈机制,连同沿肌动蛋白束的快速应力传递,在时空上使肌动蛋白拆解和纤维收缩同步。在完整的应力纤维扩张或收缩时也出现了类似的肌动蛋白重塑动力学,但时间尺度要长得多。该模型准确地描述了这些动力学,加速拆解的阈值重叠值几乎相同。最后,我们测量了静止的应力纤维,模型预测其肌动蛋白重叠是恒定的,以平衡拆解和组装。重叠确实受到调节,其值接近预测值。我们的结果表明,协调的机械信号和生化信号使延伸的肌动球蛋白组装体能够动态适应它们所传递的机械应力并指导自身的重塑。