Muzzio N E, Carballido M, Pasquale M A, González P H, Azzaroni O, Arvia A J
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas (INIFTA), Universidad Nacional de La Plata (UNLP), CONICET, Sucursal 4, Casilla de Correo 16, 1900, La Plata, Argentina.
Phys Biol. 2018 Apr 30;15(4):046001. doi: 10.1088/1478-3975/aabc2f.
The epidermal growth factor (EGF) plays a key role in physiological and pathological processes. This work reports on the influence of EGF concentration (c ) on the modulation of individual cell phenotype and cell colony kinetics with the aim of perturbing the colony front roughness fluctuations. For this purpose, HeLa cell colonies that remain confluent along the whole expansion process with initial quasi-radial geometry and different initial cell populations, as well as colonies with initial quasi-linear geometry and large cell population, are employed. Cell size and morphology as well as its adhesive characteristics depend on c . Quasi-radial colonies (QRC) expansion kinetics in EGF-containing medium exhibits a complex behavior. Namely, at the first stages of growth, the average QRC radius evolution can be described by a t diffusion term coupled with exponential growth kinetics up to a critical time, and afterwards a growth regime approaching constant velocity. The extension of each regime depends on c and colony history. In the presence of EGF, the initial expansion of quasi-linear colonies (QLCs) also exhibits morphological changes at both the cell and the colony levels. In these cases, the cell density at the colony border region becomes smaller than in the absence of EGF and consequently, the extension of the effective rim where cell duplication and motility contribute to the colony expansion increases. QLC front displacement velocity increases with c up to a maximum value in the 2-10 ng ml range. Individual cell velocity is increased by EGF, and an enhancement in both the persistence and the ballistic characteristics of cell trajectories can be distinguished. For an intermediate c collective cell displacements contribute to the roughening of the colony contours. This global dynamics becomes compatible with the standard Kardar-Parisi-Zhang growth model, although a faster colony roughness saturation in EGF-containing medium than in the control medium is observed.
表皮生长因子(EGF)在生理和病理过程中起着关键作用。本研究报告了EGF浓度(c)对单个细胞表型和细胞集落动力学调节的影响,旨在扰乱集落前沿粗糙度波动。为此,使用了在整个扩展过程中保持汇合状态、具有初始准径向几何形状和不同初始细胞群体的HeLa细胞集落,以及具有初始准线性几何形状和大量细胞群体的集落。细胞大小、形态及其粘附特性取决于c。含EGF培养基中准径向集落(QRC)的扩展动力学表现出复杂的行为。具体而言,在生长的初始阶段,平均QRC半径的演变可以用一个t扩散项与指数生长动力学相结合来描述,直到一个临界时间,之后是接近恒定速度的生长阶段。每个阶段的持续时间取决于c和集落历史。在EGF存在的情况下,准线性集落(QLC)的初始扩展在细胞和集落水平上也表现出形态变化。在这些情况下,集落边界区域的细胞密度变得比没有EGF时小,因此,细胞复制和运动对集落扩展有贡献的有效边缘的延伸增加。QLC前沿位移速度随着c的增加而增加,在2 - 10 ng/ml范围内达到最大值。EGF增加了单个细胞的速度,并且可以区分细胞轨迹的持续性和弹道特性的增强。对于中等c值,集体细胞位移导致集落轮廓的粗糙度增加。这种全局动力学与标准的Kardar-Parisi-Zhang生长模型兼容,尽管观察到含EGF培养基中的集落粗糙度饱和比对照培养基中更快。