Elliott Hunter, Fischer Robert S, Myers Kenneth A, Desai Ravi A, Gao Lin, Chen Christopher S, Adelstein Robert S, Waterman Clare M, Danuser Gaudenz
Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Cell Biology and Physiology Center, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Nat Cell Biol. 2015 Feb;17(2):137-47. doi: 10.1038/ncb3092. Epub 2015 Jan 26.
In many cases, cell function is intimately linked to cell shape control. We used endothelial cell branching morphogenesis as a model to understand the role of myosin II in shape control of invasive cells migrating in 3D collagen gels. We applied principles of differential geometry and mathematical morphology to 3D image sets to parameterize cell branch structure and local cell-surface curvature. We find that Rho/ROCK-stimulated myosin II contractility minimizes cell-scale branching by recognizing and minimizing local cell-surface curvature. Using microfabrication to constrain cell shape identifies a positive feedback mechanism in which low curvature stabilizes myosin II cortical association, where it acts to maintain minimal curvature. The feedback between regulation of myosin II by curvature and control of curvature by myosin II drives cycles of localized cortical myosin II assembly and disassembly. These cycles in turn mediate alternating phases of directionally biased branch initiation and retraction to guide 3D cell migration.
在许多情况下,细胞功能与细胞形状控制密切相关。我们以内皮细胞分支形态发生为模型,来理解肌球蛋白II在三维胶原凝胶中迁移的侵袭性细胞形状控制中的作用。我们将微分几何和数学形态学原理应用于三维图像集,以参数化细胞分支结构和局部细胞表面曲率。我们发现,Rho/ROCK刺激的肌球蛋白II收缩性通过识别并最小化局部细胞表面曲率,使细胞尺度的分支最小化。利用微加工技术来限制细胞形状,确定了一种正反馈机制,即低曲率稳定肌球蛋白II皮质关联,在那里它起到维持最小曲率的作用。曲率对肌球蛋白II的调节与肌球蛋白II对曲率的控制之间的反馈,驱动了局部皮质肌球蛋白II组装和拆卸的循环。这些循环反过来介导定向偏向分支起始和回缩的交替阶段,以引导三维细胞迁移。