Department of Growth and Differentiation of Cell Populations, Institute of Physiology, Academy of Sciences of the Czech Republic, Videnska 1082, 14220 Prague 4-Krc, Czech Republic.
Biotechnol Adv. 2011 Nov-Dec;29(6):739-67. doi: 10.1016/j.biotechadv.2011.06.004. Epub 2011 Jul 26.
The interaction of cells and tissues with artificial materials designed for applications in biotechnologies and in medicine is governed by the physical and chemical properties of the material surface. There is optimal cell adhesion to moderately hydrophilic and positively charged substrates, due to the adsorption of cell adhesion-mediating molecules (e.g. vitronectin, fibronectin) in an advantageous geometrical conformation, which makes specific sites on these molecules (e.g. specific amino acid sequences) accessible to cell adhesion receptors (e.g. integrins). Highly hydrophilic surfaces prevent the adsorption of proteins, or these molecules are bound very weakly. On highly hydrophobic materials, however, proteins are adsorbed in rigid and denatured forms, hampering cell adhesion. The wettability of the material surface, particularly in synthetic polymers, can be effectively regulated by physical treatments, e.g. by irradiation with ions, plasma or UV light. The irradiation-activated material surface can be functionalized by various biomolecules and nanoparticles, and this further enhances its attractiveness for cells and its effectiveness in regulating cell functions. Another important factor for cell-material interaction is surface roughness and surface topography. Nanostructured substrates (i.e. substrates with irregularities smaller than 100nm), are generally considered to be beneficial for cell adhesion and growth, while microstructured substrates behave more controversially (e.g. they can hamper cell spreading and proliferation but they enhance cell differentiation, particularly in osteogenic cells). A factor which has been relatively less investigated, but which is essential for cell-material interaction, is material deformability. Highly soft and deformable substrates cannot resist the tractional forces generated by cells during cell adhesion, and cells are not able to attach, spread and survive on such materials. Local variation in the physical and chemical properties of the material surface can be advantageously used for constructing patterned surfaces. Micropatterned surfaces enable regionally selective cell adhesion and directed growth, which can be utilized in tissue engineering, in constructing microarrays and in biosensorics. Nanopatterned surfaces are an effective tool for manipulating the type, number, spacing and distribution of ligands for cell adhesion receptors on the material surface. As a consequence, these surfaces are able to control the size, shape, distribution and maturity of focal adhesion plaques on cells, and thus cell adhesion, proliferation, differentiation and other cell functions.
细胞和组织与为生物技术和医学应用而设计的人工材料的相互作用受材料表面的物理和化学性质控制。适度亲水和带正电荷的基底有利于细胞的最佳粘附,这是因为细胞粘附介导分子(例如,纤连蛋白、玻连蛋白)在有利的几何构象中吸附,使这些分子上的特定位点(例如,特定的氨基酸序列)可被细胞粘附受体(例如,整合素)接近。高度亲水的表面会阻止蛋白质的吸附,或者这些分子的结合非常弱。然而,在高度疏水的材料上,蛋白质以刚性和变性的形式被吸附,从而阻碍细胞的粘附。材料表面的润湿性,特别是在合成聚合物中,可以通过物理处理(例如,离子、等离子体或紫外光辐照)有效地调节。辐照激活的材料表面可以通过各种生物分子和纳米粒子进行功能化,这进一步增强了其对细胞的吸引力和调节细胞功能的有效性。细胞与材料相互作用的另一个重要因素是表面粗糙度和表面形貌。纳米结构的基底(即,具有小于 100nm 的不规则性的基底)通常被认为有利于细胞的粘附和生长,而微结构化的基底的行为则更具争议性(例如,它们可以阻碍细胞的扩展和增殖,但可以促进细胞分化,特别是在成骨细胞中)。一个相对较少被研究的因素,但对细胞与材料的相互作用至关重要的因素是材料的可变形性。高度柔软和可变形的基底无法抵抗细胞在粘附过程中产生的牵引力,因此细胞无法在这些材料上附着、扩展和存活。材料表面物理和化学性质的局部变化可以被有利地用于构建图案化表面。微图案化表面能够实现区域选择性的细胞粘附和定向生长,这可用于组织工程、构建微阵列和生物传感器。纳米图案化表面是操纵材料表面上细胞粘附受体的配体的类型、数量、间隔和分布的有效工具。因此,这些表面能够控制细胞上粘着斑的大小、形状、分布和成熟度,从而控制细胞的粘附、增殖、分化和其他细胞功能。