Influence of systematically varied nano-scale topography on cell morphology and adhesion

Cell Commun Adhes. 2007 Sep-Oct;14(5):181-94. doi: 10.1080/15419060701755594.

Abstract

The types of cell-matrix adhesions and the signals they transduce strongly affect the cell-phenotype. We hypothesized that cells sense and respond to the three-dimensionality of their environment, which could be modulated by nano-structures on silicon surfaces. Human foreskin fibroblasts were cultured on nano-structures with different patterns (nano-post and nano-grate) and heights for 3 days. The presence of integrin alpha(5), beta(1), beta(3), paxillin and phosphorylated FAK (pFAK) were detected by western blot and immunofluorescence. Integrin beta(3) exhibited stronger signals on nano-grates. pFAK and paxillin were observed as small dot-like patterns on the cell-periphery on nano-posts and as elongated and aligned patterns on nano-grates. Collectively, our observations highlighted the presence of focal (integrin beta(1), beta(3), pFAK, paxillin), fibrillar (integrin alpha(5), beta(1)) and 3-D matrix (integrin alpha(5), beta(1), paxillin) adhesions on nano-structures. The presented nano-structures offer interesting opportunities to study the interaction of cells with topographical features comparable to the size of extracellular matrix components.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Adhesion / physiology
  • Cell Adhesion Molecules / metabolism
  • Cell Line
  • Cell Membrane / metabolism*
  • Cell Membrane / ultrastructure
  • Cell Movement / physiology
  • Cell Shape / physiology
  • Extracellular Matrix / metabolism*
  • Extracellular Matrix / ultrastructure
  • Focal Adhesion Protein-Tyrosine Kinases / metabolism
  • Focal Adhesions / metabolism
  • Focal Adhesions / ultrastructure
  • Humans
  • Integrins / metabolism
  • Nanostructures / ultrastructure*
  • Paxillin / metabolism
  • Phosphorylation
  • Receptors, Cell Surface / metabolism*
  • Signal Transduction / physiology*

Substances

  • Cell Adhesion Molecules
  • Integrins
  • Paxillin
  • Receptors, Cell Surface
  • Focal Adhesion Protein-Tyrosine Kinases