Animal cells live in a complex and diverse environment where they encounter a vast amount of information, a considerable amount of which is in the nanometer range. The surface topography that a cell encounters has a role to play in influencing cell behavior. It has been demonstrated widely that surface shape can directly influence the behavior of cells. In this paper, we discuss the interactions of animal cells with engineered nanotopography, fabricated in quartz and reverse embossed into polycaprolactone, fibroblast cells show reduced adhesion to the ordered nano pits. We show that the area of cells spreading on a structured nanotopography is reduced compared with that on a planar substrate. Furthermore, cytoskeletal organization is disrupted as indicated by a marked decrease in number and size of focal contacts.

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Abstract-Cells in the human body come across many types of information, which they respond to. Both material chemistry and topography of the surface where they adhere have an effect on cell shape, proliferation, migration, and gene expression. It is possible to create surfaces with topography at the nanometric scale to allow observation of cell-topography interactions. Previous work has shown that 100-nm-diameter pits on a 300-nm pitch can have a marked effect in reducing the adhesion of rat fibroblasts in static cultures. In the present study, a flow of cell suspension was used to investigate cell adhesion onto nanopits in dynamic conditions, by means of a parallel-plate flow chamber. A flow chamber with inner nanotopography has been designed, which allows real-time observation of the flow over the nanopits. A nanopitted pattern was successfully embossed into polymethylmethacrylate to meet the required shape of the chamber. Dynamic cell adhesion after 1 h has been quantified and compared on flat and nanopitted polymethylmethacrylate substrates. The nanopits were seen to be significantly less adhesive than the flat substrates ( 0 001), which is coherent with previous observations of static cultures.

Three fundamentally different methods were used to fabricate nanometric surface features on polymers or fused silica. Phase separation of binary polymer mixes resulted in randomly distributed features whose depth and shape could be tightly controlled over large areas. Colloidal resist patterned large areas randomly and uniformly with very fine spikes. In contrast e-beam and reactive ion etching were used to create a set of regular spaced pillars on an orthogonal pattern. Some of the surfaces were replicated by in situ polymerization, solvent casting, embossing or melt molding onto polystyrene (PS) or ε–poly caprolactone (ε–PCL). Nanometric features down to 60nm were imprinted onto the polymers with high fidelity. Cells were seeded onto the nanometric surfaces and adhesion, morphology and cytoskeleton investigated. Cells respond to regular features of 170/80nm (width/depth) with reduced adhesion and changes in overall morphology and cytoskeleton. Small nanofeatures (13nm, 35nm depth) made by phase separation on the other hand increased adhesion and promoted cytoskeletal differentiation. The responses of the cells are indicative that nanometric surface features are useful modifications on scaffolds for tissue engineering or on medical implants.

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