A parallel-plate flow chamber to study initial cell adhesion on a nanofeatured surface

被引:48
作者
Martines, E [1 ]
McGhee, K
Wilkinson, C
Curtis, A
机构
[1] Univ Glasgow, Ctr Cell Engn, Inst Biomed & Life Sci, Glasgow G12 8QQ, Lanark, Scotland
[2] Univ Glasgow, Dept Elect & Elect Engn, Glasgow G12 8QQ, Lanark, Scotland
基金
英国工程与自然科学研究理事会;
关键词
cell adhesion; embossing; flow; nanotopography; polymethylmethacrylate; topography;
D O I
10.1109/TNB.2004.828268
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 (p < 0.001), which is coherent with previous observations of static cultures.
引用
收藏
页码:90 / 95
页数:6
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