4.8 Article

Biological effects of cobalt-chromium nanoparticles and ions on dural fibroblasts and dural epithelial cells

期刊

BIOMATERIALS
卷 34, 期 14, 页码 3547-3558

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2013.01.023

关键词

Cobalt-chromium; Meninges; Cell viability; Nanoparticles; Cytokines; Oxidative stress

资金

  1. National Institutes of Health [R01-AR052653-01]
  2. Leeds Centre of Excellence in Medical Engineering
  3. Wellcome Trust and EPSRC [WT088908/z/091z]
  4. Biotechnology and Biological Sciences Research Council [BB/F011105/1] Funding Source: researchfish
  5. Engineering and Physical Sciences Research Council [EP/J017620/1, EP/I019103/1, EP/G032483/1, EP/F043872/1, EP/K029592/1] Funding Source: researchfish
  6. Medical Research Council [G0701221] Funding Source: researchfish
  7. National Institute for Health Research [NF-SI-0611-10096] Funding Source: researchfish
  8. BBSRC [BB/F011105/1] Funding Source: UKRI
  9. EPSRC [EP/I019103/1, EP/J017620/1, EP/G032483/1, EP/F043872/1, EP/K029592/1] Funding Source: UKRI
  10. MRC [G0701221] Funding Source: UKRI

向作者/读者索取更多资源

The introduction of metal-on-metal total disc replacements motivated studies to evaluate the effects of cobalt-chromium (CoCr) nanoparticles on cells of the dura mater. Porcine fibroblasts and epithelial cells isolated from the dura mater were cultured with clinically-relevant CoCr nanoparticles and the ions, generated by the particles over 24 h, at doses up to 121 mu m(3)per cell. Cell viability and production of proinflammatory cytokines was assessed over 4 days. The capacity of the particles to induce oxidative stress in the cells was evaluated at 24 h. The CoCr particles and their ions significantly reduced the viability of the dural epithelial cells in a dose-dependent manner but not the fibroblasts. Both cell types secreted IL-8 in response to particle exposure at doses of 60.5 mu m(3) (epithelial cells) and 121 mu m(3) (fibroblasts, epithelial cells) per cell. No significant release of IL-6 was observed in both cell types at any dose. Reactive oxygen species were induced in both cell types at 50 mu m(3) per cell after 24 h exposure. The data suggested novel differences in the resistance of the dural epithelial cells and fibroblasts to CoCr nanoparticle/ion toxicity and demonstrated the inflammatory potential of the particles. The data contributes to a greater understanding of the potential biological consequences of the use of metal-on-metal total disc prostheses. (C) 2013 Elsevier Ltd. All rights reserved.

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