Using Surface Plasmon Resonance Imaging to Probe Dynamic Interactions Between Cells and Extracellular Matrix

被引:29
|
作者
Peterson, Alexander W. [1 ]
Halter, Michael [1 ]
Tona, Alessandro [1 ]
Bhadriraju, Kiran [1 ]
Plant, Anne L. [1 ]
机构
[1] NIST, Cell Syst Sci Grp, Div Biochem Sci, Gaithersburg, MD 20899 USA
关键词
vascular smooth muscle cells; fibronectin; imaging; image analysis; label-free; surface plasmon resonance; cell spreading; ruffling; COUPLED EMISSION; MICROSCOPY; ADHESION; HYBRIDIZATION; FIBRONECTIN; CONTACTS; BINDING; PROTEIN; DNA;
D O I
10.1002/cyto.a.20938
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Spatially resolved details of the interactions of cells with a fibronectin modified surface were examined using surface plasmon resonance imaging (SPRI). SPRI is a label-free technique that is based on the spatial measurement of interfacial refractive index. SPRI is sensitive to short range interactions between cells and their substratum. The high contrast in SPR signal between cell edges and substratum facilitates identification of cell edges and segmentation of cell areas. With this novel technique, we demonstrate visualization of cell-substratum interactions, and how cell-substratum interactions change over time as cells spread, migrate, and undergo membrane ruffling. Published 2010 Wiley-Liss, Inc.(dagger)
引用
收藏
页码:895 / 903
页数:9
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