Surface plasma functionalization influences macrophage behavior on carbon nanowalls

Mater Sci Eng C Mater Biol Appl. 2015 Mar:48:118-25. doi: 10.1016/j.msec.2014.11.064. Epub 2014 Dec 2.

Abstract

The surfaces of carbon nanowall samples as scaffolds for tissue engineering applications were treated with oxygen or nitrogen plasma to improve their wettability and to functionalize their surfaces with different functional groups. X-ray photoelectron spectroscopy and water contact angle results illustrated the effective conversion of the carbon nanowall surfaces from hydrophobic to hydrophilic and the incorporation of various amounts of carbon, oxygen and nitrogen functional groups during the treatments. The early inflammatory responses elicited by un-treated and modified carbon nanowall surfaces were investigated by quantifying tumor necrosis factor-alpha and macrophage inflammatory protein-1 alpha released by attached RAW 264.7 macrophage cells. Scanning electron microscopy and fluorescence studies were employed to investigate the changes in macrophage morphology and adhesive properties, while MTT assay was used to quantify cell proliferation. All samples sustained macrophage adhesion and growth. In addition, nitrogen plasma treatment was more beneficial for cell adhesion in comparison with un-modified carbon nanowall surfaces. Instead, oxygen plasma functionalization led to increased macrophage adhesion and spreading suggesting a more activated phenotype, confirmed by elevated cytokine release. Thus, our findings showed that the chemical surface alterations which occur as a result of plasma treatment, independent of surface wettability, affect macrophage response in vitro.

Keywords: Carbon nanowall; Functional group; Inflammatory response; Macrophage; Plasma treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Animals
  • Biocompatible Materials / chemistry
  • Carbon / chemistry*
  • Cell Adhesion
  • Cell Line
  • Cell Proliferation
  • Cell Survival
  • Chemokine CCL3 / metabolism
  • Cytoskeleton / metabolism
  • Hydrophobic and Hydrophilic Interactions
  • Macrophage Inflammatory Proteins / metabolism
  • Macrophages / cytology
  • Macrophages / physiology*
  • Mice
  • Nanostructures / chemistry*
  • Nitrogen / chemistry
  • Oxygen / chemistry
  • Photoelectron Spectroscopy
  • Surface Properties
  • Tissue Engineering / methods
  • Tumor Necrosis Factor-alpha / metabolism
  • Wettability

Substances

  • Actins
  • Biocompatible Materials
  • Chemokine CCL3
  • Macrophage Inflammatory Proteins
  • Tumor Necrosis Factor-alpha
  • Carbon
  • Nitrogen
  • Oxygen