Piotrowski-Daspit Alexandra S, Nerger Bryan A, Wolf Abraham E, Sundaresan Sankaran, Nelson Celeste M
Department of Chemical and Biological Engineering, Princeton University, Princeton, New Jersey.
Department of Chemical and Biological Engineering, Princeton University, Princeton, New Jersey; Department of Molecular Biology, Princeton University, Princeton, New Jersey.
Biophys J. 2017 Aug 8;113(3):702-713. doi: 10.1016/j.bpj.2017.06.046.
Aligned fibers of extracellular matrix (ECM) affect the direction, efficiency, and persistence of migrating cells. To uncover the mechanisms by which multicellular tissues align their surrounding ECM before migration, we used an engineered three-dimensional culture model to investigate the dynamics of ECM alignment around tissues of defined geometry. Analysis of ECM alignment over time revealed that tissues rapidly reorganize their surrounding matrix, with a characteristic time that depends on the type of cell and the initial tissue geometry. We found that matrix metalloproteinase activity is not required for matrix alignment before cell migration. Instead, alignment is driven by Rho-mediated cytoskeletal contractility and accelerated by propagation of tension through intercellular adhesions. Our data suggest that multicellular tissues align their surrounding matrix by pulling collectively to exert strain, which is primarily a physical process. Consistently, the pattern of matrix alignment depends on tissue geometry and the resulting distribution of mechanical strain, with asymmetric tissues generating a higher degree of matrix alignment along their longest axes. The rapid ability of multicellular tissues to physically remodel their matrix enables their constituent cells to migrate efficiently along aligned fibers and to quickly change their direction according to other microenvironmental cues, which is important for both normal and disease processes.
细胞外基质(ECM)的排列纤维会影响迁移细胞的方向、效率和持久性。为了揭示多细胞组织在迁移前使其周围ECM排列的机制,我们使用了一种工程化的三维培养模型来研究特定几何形状组织周围ECM排列的动力学。对ECM随时间排列的分析表明,组织会迅速重组其周围的基质,其特征时间取决于细胞类型和初始组织几何形状。我们发现,在细胞迁移之前,基质金属蛋白酶活性对于基质排列并非必需。相反,排列是由Rho介导的细胞骨架收缩性驱动的,并通过细胞间粘附传递张力而加速。我们的数据表明,多细胞组织通过集体牵拉以施加应变来使其周围基质排列,这主要是一个物理过程。一致地,基质排列模式取决于组织几何形状以及由此产生的机械应变分布,不对称组织沿其最长轴产生更高程度的基质排列。多细胞组织快速物理重塑其基质的能力使其组成细胞能够沿着排列的纤维高效迁移,并根据其他微环境线索快速改变方向,这对于正常和疾病过程都很重要。