Inflammatory response to nano- and microstructured hydroxyapatite

PLoS One. 2015 Apr 2;10(3):e0120381. doi: 10.1371/journal.pone.0120381. eCollection 2015.

Abstract

The proliferation and activation of leukocytes upon contact with a biomaterial play a crucial role in the degree of inflammatory response, which may then determine the clinical failure or success of an implanted biomaterial. The aim of this study was to evaluate whether nano- and microstructured biomimetic hydroxyapatite substrates can influence the growth and activation of macrophage-like cells. Hydroxyapatite substrates with different crystal morphologies consisting of an entangled network of plate-like and needle-like crystals were evaluated. Macrophage proliferation was evaluated on the material surface (direct contact) and also in extracts i.e. media modified by the material (indirect contact). Additionally, the effect of supplementing the extracts with calcium ions and/or proteins was investigated. Macrophage activation on the substrates was evaluated by quantifying the release of reactive oxygen species and by morphological observations. The results showed that differences in the substrate's microstructure play a major role in the activation of macrophages as there was a higher release of reactive oxygen species after culturing the macrophages on plate-like crystals substrates compared to the almost non-existent release on needle-like substrates. However, the difference in macrophage proliferation was ascribed to different ionic exchanges and protein adsorption/retention from the substrates rather than to the texture of materials.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biocompatible Materials / adverse effects
  • Biocompatible Materials / chemistry
  • Cell Line
  • Cell Proliferation
  • Cells, Cultured
  • Durapatite / adverse effects*
  • Durapatite / chemistry*
  • Inflammation / etiology*
  • Inflammation / metabolism
  • Macrophage Activation
  • Macrophages / immunology
  • Macrophages / metabolism
  • Mice
  • Nanostructures* / chemistry
  • Nanostructures* / ultrastructure
  • Particle Size
  • Reactive Oxygen Species / metabolism

Substances

  • Biocompatible Materials
  • Reactive Oxygen Species
  • Durapatite

Grants and funding

This work was funded by Marie Curie Actions FP7-PEOPLE-2011-COFUND (GROWTH 291795) via the VINNOVA programme Mobility for Growth, Lars Hiertas Minne Foundation (FO2013-0337 project), STINT (IG2011-2047 project), and Ollie och Elof Ericssons Stifelse för Vetenskaplig Forskning. The authors acknowledge the Spanish Government for financial support through project MAT2012-38438-003-01, co-funded by the EU through European Regional Development Funds. Support for the research of MPG was received through the prize ‘‘ICREA Academia’’ for excellence in research, funded by the Generalitat de Catalunya. Part of this work was performed at the BioMat facility/ Science for Life Laboratory at Uppsala University. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.