Hulsman Marc, Hulshof Frits, Unadkat Hemant, Papenburg Bernke J, Stamatialis Dimitrios F, Truckenmüller Roman, van Blitterswijk Clemens, de Boer Jan, Reinders Marcel J T
Delft Bioinformatics Lab, Delft University of Technology, Mekelweg 4, Delft 2628 CD, The Netherlands.
MIRA Institute for Biomedical Technology and Technical Medicine, Department of Tissue Regeneration, University of Twente, P.O. Box 217, Enschede 7500 AE, The Netherlands; MIRA Institute for Biomedical Technology and Technical Medicine, Department of Biomaterials Science and Technology, University of Twente, P.O. Box 217, Enschede 7500 AE, The Netherlands.
Acta Biomater. 2015 Mar;15:29-38. doi: 10.1016/j.actbio.2014.12.019. Epub 2014 Dec 30.
Surface topographies of materials considerably impact cellular behavior as they have been shown to affect cell growth, provide cell guidance, and even induce cell differentiation. Consequently, for successful application in tissue engineering, the contact interface of biomaterials needs to be optimized to induce the required cell behavior. However, a rational design of biomaterial surfaces is severely hampered because knowledge is lacking on the underlying biological mechanisms. Therefore, we previously developed a high-throughput screening device (TopoChip) that measures cell responses to large libraries of parameterized topographical material surfaces. Here, we introduce a computational analysis of high-throughput materiome data to capture the relationship between the surface topographies of materials and cellular morphology. We apply robust statistical techniques to find surface topographies that best promote a certain specified cellular response. By augmenting surface screening with data-driven modeling, we determine which properties of the surface topographies influence the morphological properties of the cells. With this information, we build models that predict the cellular response to surface topographies that have not yet been measured. We analyze cellular morphology on 2176 surfaces, and find that the surface topography significantly affects various cellular properties, including the roundness and size of the nucleus, as well as the perimeter and orientation of the cells. Our learned models capture and accurately predict these relationships and reveal a spectrum of topographies that induce various levels of cellular morphologies. Taken together, this novel approach of high-throughput screening of materials and subsequent analysis opens up possibilities for a rational design of biomaterial surfaces.
材料的表面形貌对细胞行为有重大影响,因为已证明它们会影响细胞生长、为细胞提供引导,甚至诱导细胞分化。因此,为了在组织工程中成功应用,生物材料的接触界面需要进行优化,以诱导所需的细胞行为。然而,生物材料表面的合理设计受到严重阻碍,因为缺乏对潜在生物学机制的了解。因此,我们之前开发了一种高通量筛选装置(TopoChip),用于测量细胞对大量参数化地形材料表面文库的反应。在这里,我们引入了对高通量材料组数据的计算分析,以捕捉材料表面形貌与细胞形态之间的关系。我们应用强大的统计技术来找到最能促进某种特定细胞反应的表面形貌。通过用数据驱动的建模增强表面筛选,我们确定表面形貌的哪些属性会影响细胞的形态属性。有了这些信息,我们构建模型来预测细胞对尚未测量的表面形貌的反应。我们分析了2176个表面上的细胞形态,发现表面形貌显著影响各种细胞属性,包括细胞核的圆度和大小,以及细胞的周长和方向。我们所学的模型捕捉并准确预测了这些关系,并揭示了一系列能诱导不同水平细胞形态的形貌。综上所述,这种材料高通量筛选及后续分析的新方法为生物材料表面的合理设计开辟了可能性。