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Fibronectin adsorption, cell adhesion, and proliferation on nanostructured tantalum surfaces

A. Dolatshahi-Pirouz, T. Jensen, David Christian Kraft, Morten Foss*, Peter Kingshott, John Lundsgaard Hansen, Arne Nylandsted Larsen, Jacques Chevallier, Flemming Besenbacher

*Corresponding author for this work
177 Citations (Scopus)

Abstract

The interaction between dental pulp derived mesenchymal stem cells (DP-MSCs) and three different tantalum nanotopographies with and without a fibronectin coating is examined: sputter-coated tantalum surfaces with low surface roughness <0.2 nm, hut-nanostructured surfaces with a height of 2.9 ± 0.6 nm and a width of 35 ± 8 nm, and dome structures with a height of 13 ± 2 nm and a width of 52 ± 14 nm. Using ellipsometry, the adsorption and the availability of fibronectin cell-binding domains on the tantalum surfaces were examined, as well as cellular attachment, proliferation, and vinculin focal adhesion spot assembly on the respective surfaces. The results showed the highest fibronectin mass uptake on the hut structures, with a slightly higher availability of cell-binding domains and the most pronounced formation of vinculin focal adhesion spots as compared to the other surfaces. The proliferation of DP-MSCs was found to be significantly higher on dome and hut surfaces coated with fibronectin compared to the uncoated flat tantalum surfaces. Consequently, the results presented in this study indicate that fibronectin-coated nanotopographies with a vertical dimension of less than 5 nm influence cell adhesion. This rather interesting behavior is argued to originate from the more available fibronectin cell-binding domains observed on the hut structures.

Original languageEnglish
JournalACS Nano
Volume4
Issue number5
Pages (from-to)2874-2882
Number of pages9
ISSN1936-0851
DOIs
Publication statusPublished - 25 May 2010
Externally publishedYes

Keywords

  • Cell adhesion
  • Fibronectin
  • Mesenchymal stem cells
  • Nanotopography
  • Protein adsorption
  • Tantalum
  • Tissue engineering

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