Controlling fibroblast adhesion with pH modified polyelectrolyte multilayers

Int J Artif Organs. 2011 Feb;34(2):185-91. doi: 10.5301/ijao.2011.6395.

Abstract

Tissue cells need to adhere to a biomaterial surface to promote their growth and differentiation and, thus, foster the integration of implants. As a result, surface features and their modification play an important role in biomedical applications. In this study, the layer-by-layer (LbL) technique was used to design self-assembled polyelectrolyte multilayer (PEM) coatings of polyethyleneimine (PEI) and heparin (HEP) on glass, which will control the adhesion of primary human dermal fibroblasts in a model system. The study showed that, among other surface features, the wettability of surfaces can be controlled by changing the conditions during multilayer self-assembly. Here, the pH value of the HEP solution was adjusted to acidic or alkaline values for terminal layers, which also led to a change in multilayer growth. Further, the study revealed that plain terminal layers were rather cytophobic. Upon pre-adsorption of fibronectin (FN), a clear effect on cell adhesion and morphology in dependence on the pH setup was evident. Proliferation studies clearly showed that terminal layers, which impaired cell adhesion, also inhibited growth of human fibroblasts under serum-conditions. On the other hand, on layers with pronounced cell adhesion an elevated cell growth was also observed. As a result, HEP terminated multilayers are interesting for applications requiring cell repellent properties, whereas PEI terminated multilayers could be used to promote cell adhesion and growth on implant surfaces.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adhesiveness
  • Adsorption
  • Biocompatible Materials*
  • Cell Adhesion*
  • Cell Proliferation
  • Cells, Cultured
  • Fibroblasts / physiology*
  • Fibronectins / metabolism
  • Heparin / chemistry*
  • Humans
  • Hydrogen-Ion Concentration
  • Microscopy, Confocal
  • Polyethyleneimine / chemistry*
  • Tissue Engineering / methods*
  • Tissue Scaffolds*
  • Wettability

Substances

  • Biocompatible Materials
  • Fibronectins
  • Polyethyleneimine
  • Heparin