Lücker Petra B, Javaherian Sahar, Soleas John P, Halverson Duncan, Zandstra Peter W, McGuigan Alison P
Department of Chemical Engineering and Applied Chemistry, University of Toronto, 200 College St., Toronto, Ontario, M5T 3J9, Canada; Institute of Biomaterials and Biomedical Engineering, University of Toronto, Toronto, Ontario, Canada.
Biotechnol Bioeng. 2014 Dec;111(12):2537-48. doi: 10.1002/bit.25298. Epub 2014 Jul 29.
Grooved substrates are commonly used to guide cell alignment and produce in vitro tissues that mimic certain aspects of in vivo cellular organization. These more sophisticated tissues provide valuable in vitro models for testing drugs and for dissecting out molecular mechanisms that direct tissue organization. To increase the accessibility of these tissue models we describe a simple and yet reproducible strategy to produce 1 µm-spaced grooved well plates suitable for conducting automated analysis of cellular responses. We characterize the alignment of four human cell types: retinal epithelial cells, umbilical vein endothelial cells, foreskin fibroblasts, and human pluripotent stem-cell-derived cardiac cells on grooves. We find all cells align along the grooves to differing extents at both sparse and confluent densities. To increase the sophistication of in vitro tissue organization possible, we also created hybrid substrates with controlled patterns of microgrooved and flat regions that can be identified in real-time using optical microscopy. Using our hybrid patterned surfaces we explore: (i) the ability of neighboring cells to provide a template to organize surrounding cells that are not directly exposed to grooved topographic cues, and (ii) the distance over which this template effect can operate in confluent cell sheets. We find that in fibroblast sheets, but not epithelial sheets, cells aligned on grooves can direct alignment of neighboring cells in flat regions over a limited distance of approximately 200 μm. Our hybrid surface plate provides a novel tool for studying the collective response of groups of cells exposed to differential topographical cues.
带凹槽的基质常用于引导细胞排列,并生成模仿体内细胞组织某些方面的体外组织。这些更复杂的组织为测试药物和剖析指导组织形成的分子机制提供了有价值的体外模型。为了提高这些组织模型的可及性,我们描述了一种简单且可重复的策略,用于生产间距为1微米的带凹槽孔板,适合对细胞反应进行自动化分析。我们对四种人类细胞类型在凹槽上的排列进行了表征:视网膜上皮细胞、脐静脉内皮细胞、包皮成纤维细胞和人多能干细胞衍生的心脏细胞。我们发现,在稀疏和汇合密度下,所有细胞都在不同程度上沿着凹槽排列。为了提高体外组织形成的复杂性,我们还创建了具有可控微凹槽和平坦区域图案的混合基质,可通过光学显微镜实时识别。利用我们的混合图案表面,我们探索了:(i)相邻细胞为未直接暴露于带凹槽地形线索的周围细胞提供组织模板的能力,以及(ii)这种模板效应在汇合细胞片中能够发挥作用的距离。我们发现,在成纤维细胞片中,而非上皮细胞片中,在凹槽上排列的细胞可以在大约200微米的有限距离内引导平坦区域中相邻细胞的排列。我们的混合表面板为研究暴露于不同地形线索的细胞群的集体反应提供了一种新工具。