Friedl Peter, Mayor Roberto
Department of Cell Biology, Radboud University Medical Centre, Nijmegen 6525GA, The Netherlands.
David H. Koch Center for Applied Research of Genitourinary Cancers, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030.
Cold Spring Harb Perspect Biol. 2017 Apr 3;9(4):a029199. doi: 10.1101/cshperspect.a029199.
Collective cell migration critically depends on cell-cell interactions coupled to a dynamic actin cytoskeleton. Important cell-cell adhesion receptor systems implicated in controlling collective movements include cadherins, immunoglobulin superfamily members (L1CAM, NCAM, ALCAM), Ephrin/Eph receptors, Slit/Robo, connexins and integrins, and an adaptive array of intracellular adapter and signaling proteins. Depending on molecular composition and signaling context, cell-cell junctions adapt their shape and stability, and this gradual junction plasticity enables different types of collective cell movements such as epithelial sheet and cluster migration, branching morphogenesis and sprouting, collective network migration, as well as coordinated individual-cell migration and streaming. Thereby, plasticity of cell-cell junction composition and turnover defines the type of collective movements in epithelial, mesenchymal, neuronal, and immune cells, and defines migration coordination, anchorage, and cell dissociation. We here review cell-cell adhesion systems and their functions in different types of collective cell migration as key regulators of collective plasticity.
集体细胞迁移关键依赖于与动态肌动蛋白细胞骨架相关联的细胞间相互作用。参与控制集体运动的重要细胞间粘附受体系统包括钙黏蛋白、免疫球蛋白超家族成员(L1细胞粘附分子、神经细胞粘附分子、活化白细胞粘附分子)、 Ephrin/Eph受体、Slit/Robo、连接蛋白和整合素,以及一系列适应性的细胞内衔接蛋白和信号蛋白。根据分子组成和信号背景,细胞间连接会调整其形状和稳定性,这种逐渐变化的连接可塑性使得不同类型的集体细胞运动成为可能,如上皮片层和细胞簇迁移、分支形态发生和出芽、集体网络迁移,以及协调的单个细胞迁移和流动。因此,细胞间连接组成和更新的可塑性决定了上皮细胞、间充质细胞、神经元细胞和免疫细胞中集体运动的类型,并决定了迁移的协调性、锚定和细胞解离。我们在此综述细胞间粘附系统及其在不同类型集体细胞迁移中的功能,它们是集体可塑性的关键调节因子。