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Cell shape and spreading of stromal (mesenchymal) stem cells cultured on fibronectin coated gold and hydroxyapatite surfaces

Year: 2011

Journal: Colloids and Surfaces B: Biointerfaces, Volume 84, Issue 1, 1 May 2011, Pages 18-25, 20110317

Authors: Dolatshahi-Pirouz A. 1, Jensen T.H.L. 1 3, Kolind K. 1, Bünger C. 3, Kassem M. 4 5, Foss M. 1, Besenbacher M. 1 2

Last authors: F. Besenbacher

Organizations: 1 Interdisciplinary Nanoscience Center (iNANO), Aarhus University, DK-8000 Aarhus C, Denmark 2 Department of Physics and Astronomy, Aarhus University, DK-8000 Aarhus C, Denmark 3 Orthopedic Research Laboratory, Clinical Institute, Aarhus University, DK-8000 Aarhus C, Denmark 4 Odense Univ Hosp, Dept Endocrinol & Metab, DK-5000 Odense C, Denmark 5 Stem Cell Unit, King Saud University, Riyadh, Saudi Arabia

Country: Denmark

In order to identify the cellular mechanisms leading to the biocompatibility of hydroxyapatite implants, we studied the interaction of human bone marrow derived stromal (mesenchymal) stem cells (hMSCs) with fibronectin-coated gold (Au) and hydroxyapatite (HA) surfaces. The adsorption of fibronectin was monitored by Quartz Crystal Microbalance with Dissipation (QCM -D) at two different concentrations, 20 μg/ml and 200 μg/ml, and the fibronectin adsorption experiments were complemented with antibody measurements. The QCM -D results show that the surface mass uptake is largest on the Au surfaces, while the number of polyclonal and monoclonal antibodies directed against the cell-binding domain (CB-domain) on the fibronectin (Fn) is significantly larger on the (HA) surfaces. Moreover, a higher number of antibodies bound to the fibronectin coatings formed from the highest bulk fibronection concentration. In subsequent cell studies with hMSC's we studied the cell spreading, cytoskeletal organization and cell morphology on the respective surfaces. When the cells were adsorbed on the uncoated substrates, a diffuse cell actin cytoskeleton was revealed, and the cells had a highly elongated shape. On the fibronectin coated surfaces the cells adapted to a more polygonal shape with a well-defined actin cytoskeleton, while a larger cell area and roundness values were observed for cells cultured on the coated surfaces. Among the coated surfaces a slightly larger cell area and roundness values was observed on HA as compared to Au. Moreover, the results revealed that the morphology of cells cultured on fibronectin coated HA surfaces were less irregular. In summary we find that fibronectin adsorbs in a more activated state on the HA surfaces, resulting in a slightly different cellular response as compared to the fibronectin coated Au surfaces.