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Why the dish makes a difference: Quantitative comparison of polystyrene culture surfaces

机译:为什么这道菜与众不同:聚苯乙烯培养物表面的定量比较

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There is wide anecdotal recognition that biological cell viability and behavior can vary significantly as a function of the source of commercial tissue culture polystyrene (TCPS) culture vessels to which those cells adhere. However, this marked material dependency is typically resolved by selecting and then consistently using the same manufacturer's product-following protocol-rather than by investigating the material properties that may be responsible for such experimental variation. Here, we quantified several physical properties of TCPS surfaces obtained from a wide range of commercial sources and processing steps, through the use of atomic force microscopy (AFM)-based imaging and analysis, goniometry and protein adsorption quantification. We identify qualitative differences in surface features, as well as quantitative differences in surface roughness and wettability that cannot be attributed solely to differences in surface chemistry. We also find significant differences in cell morphology and proliferation among cells cultured on different TCPS surfaces, and resolve a correlation between nanoscale surface roughness and cell proliferation rate for both cell types considered. Interestingly, AFM images of living adherent cells on these nanotextured surfaces demonstrate direct interactions between cellular protrusions and topographically distinct features. These results illustrate and quantify the significant differences in material surface properties among these ubiquitous materials, allowing us to better understand why the dish can make a difference in biological experiments.
机译:有广泛的传闻认为,生物细胞的活力和行为可能会随着这些细胞所附着的商业组织培养聚苯乙烯(TCPS)培养容器的来源而发生显着变化。但是,这种明显的材料依赖性通常是通过选择并随后使用同一制造商的产品(遵循协议)来解决的,而不是通过调查可能造成此类实验差异的材料特性来解决的。在这里,我们通过使用基于原子力显微镜(AFM)的成像和分析,测角法和蛋白质吸附定量,对从广泛的商业来源和加工步骤获得的TCPS表面的几种物理性质进行了量化。我们确定了表面特征的定性差异,以及表面粗糙度和润湿性的定量差异,这些差异不能仅归因于表面化学性质的差异。我们还发现在不同TCPS表面上培养的细胞之间细胞形态和增殖的显着差异,并解决了考虑的两种细胞类型的纳米级表面粗糙度和细胞增殖速率之间的相关性。有趣的是,这些纳米纹理化表面上的活细胞的AFM图像显示出细胞突起与形貌独特的特征之间的直接相互作用。这些结果说明并量化了这些无处不在的材料之间在材料表面特性方面的显着差异,使我们能够更好地理解该培养皿为何可以在生物学实验中发挥作用。

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