Löber Jakob, Ziebert Falko, Aranson Igor S
Institut für Theoretische Physik, Hardenbergstrasse 36, EW 7-1, Technische Universität Berlin, 10623 Berlin, Germany.
1] Physikalisches Institut, Albert-Ludwigs-Universität Freiburg, Hermann-Herder-Strasse 3, 79104 Freiburg, Germany [2] Institut Charles Sadron, CNRS-UPR22, 23 rue du Loess, 67034 Strasbourg Cedex 2, France.
Sci Rep. 2015 Mar 17;5:9172. doi: 10.1038/srep09172.
Collective migration of eukaryotic cells plays a fundamental role in tissue growth, wound healing and immune response. The motion, arising spontaneously or in response to chemical and mechanical stimuli, is also important for understanding life-threatening pathologies, such as cancer and metastasis formation. We present a phase-field model to describe the movement of many self-organized, interacting cells. The model takes into account the main mechanisms of cell motility - acto-myosin dynamics, as well as substrate-mediated and cell-cell adhesion. It predicts that collective cell migration emerges spontaneously as a result of inelastic collisions between neighboring cells: collisions lead to a mutual alignment of the cell velocities and to the formation of coherently-moving multi-cellular clusters. Small cell-to-cell adhesion, in turn, reduces the propensity for large-scale collective migration, while higher adhesion leads to the formation of moving bands. Our study provides valuable insight into biological processes associated with collective cell motility.
真核细胞的集体迁移在组织生长、伤口愈合和免疫反应中起着基础性作用。这种自发产生或对化学和机械刺激作出反应的运动,对于理解诸如癌症和转移形成等危及生命的病理状况也很重要。我们提出了一个相场模型来描述许多自组织、相互作用细胞的运动。该模型考虑了细胞运动的主要机制——肌动蛋白-肌球蛋白动力学,以及底物介导的和细胞间的粘附。它预测,相邻细胞之间的非弹性碰撞会自发产生集体细胞迁移:碰撞导致细胞速度相互对齐,并形成协同移动的多细胞簇。反过来,较小的细胞间粘附会降低大规模集体迁移的倾向,而较高的粘附则会导致移动带的形成。我们的研究为与集体细胞运动相关的生物学过程提供了有价值的见解。