International Center for Materials Nanoarchitectonics (WPI-MANA), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.
International Center for Materials Nanoarchitectonics (WPI-MANA), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.
Biomaterials. 2018 Jul;169:72-84. doi: 10.1016/j.biomaterials.2018.03.045. Epub 2018 Mar 27.
Epithelial cells migrate as multicellular units. The directionality and speed of these units are determined by actively moving leader cells. It is important to understand how external cues affect the appearance of these leader cells in physiological and pathological processes. However, the impact of extracellular matrices (ECMs) is still controversial, because physically-adsorbed ECM proteins are amenable to protein remodeling, and uncontrolled cluster geometry can vary migration phenotypes. Here, we demonstrate a photoactivatable substrate, which we used to study the impact of a cyclic Arg-Gly-Asp (cRGD) ligand on leader cell formation in MDCK cells. This robust platform allowed us to investigate the effect of cRGD density on leader cell formation, in any given cluster geometry, with minimized ECM remodeling. Our results show a biphasic response of leader cell appearance upon reducing the surface cRGD density. The increase, in leader cell appearance, within the higher density range, is not only associated with the weakening of circumferential actomyosin belts, but also reduction of cellular mechanical tension and intercellular junctional E-cadherin. These results indicate that cRGD-mediated cell-ECM interactions positively regulate mechanical and biochemical coupling within cell clusters; both are critical for the coordination of cell collectives and eventual reduction in the appearance of leader cells.
上皮细胞作为多细胞单位迁移。这些单位的方向性和速度由主动移动的先导细胞决定。了解外部线索如何影响生理和病理过程中这些先导细胞的出现是很重要的。然而,细胞外基质 (ECM) 的影响仍存在争议,因为物理吸附的 ECM 蛋白容易发生蛋白质重塑,并且不受控制的簇状几何形状会改变迁移表型。在这里,我们展示了一种光活化底物,我们用它来研究环精氨酸-甘氨酸-天冬氨酸 (cRGD) 配体对 MDCK 细胞中先导细胞形成的影响。这个强大的平台使我们能够在任何给定的簇状几何形状下,在最小化 ECM 重塑的情况下,研究 cRGD 密度对先导细胞形成的影响。我们的结果表明,在降低表面 cRGD 密度时,先导细胞的出现呈现出双相反应。在较高密度范围内,先导细胞出现的增加不仅与周向肌动球蛋白带的减弱有关,还与细胞机械张力和细胞间连接 E-钙粘蛋白的减少有关。这些结果表明,cRGD 介导的细胞-ECM 相互作用正向调节细胞簇内的机械和生化偶联;这两者对于细胞群体的协调以及最终减少先导细胞的出现都是至关重要的。