Distinctive glial and neuronal interfacing on nanocrystalline diamond

PLoS One. 2014 Mar 24;9(3):e92562. doi: 10.1371/journal.pone.0092562. eCollection 2014.

Abstract

Direct electrode/neuron interfacing is a key challenge to achieve high resolution of neuronal stimulation required for visual prostheses. Neuronal interfacing on biomaterials commonly requires the presence of glial cells and/or protein coating. Nanocrystalline diamond is a highly mechanically stable biomaterial with a remarkably large potential window for the electrical stimulation of tissues. Using adult retinal cell cultures from rats, we found that glial cells and retinal neurons grew equally well on glass and nanocrystalline diamond. The use of a protein coating increased cell survival, particularly for glial cells. However, bipolar neurons appeared to grow even in direct contact with bare diamond. We investigated whether the presence of glial cells contributed to this direct neuron/diamond interface, by using purified adult retinal ganglion cells to seed diamond and glass surfaces with and without protein coatings. Surprisingly, these fully differentiated spiking neurons survived better on nanocrystalline diamond without any protein coating. This greater survival was indicated by larger cell numbers and the presence of longer neurites. When a protein pattern was drawn on diamond, neurons did not grow preferentially on the coated area, by contrast to their behavior on a patterned glass. This study highlights the interesting biocompatibility properties of nanocrystalline diamond, allowing direct neuronal interfacing, whereas a protein coating was required for glial cell growth.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biocompatible Materials / chemistry
  • Biocompatible Materials / pharmacology
  • Cell Survival / drug effects
  • Diamond / chemistry
  • Diamond / pharmacology*
  • Electric Stimulation
  • Materials Testing*
  • Nanoparticles*
  • Neuroglia / cytology*
  • Neuroglia / drug effects*
  • Rats
  • Retinal Ganglion Cells / cytology*
  • Retinal Ganglion Cells / drug effects*

Substances

  • Biocompatible Materials
  • Diamond

Grants and funding

This work was supported by INSERM, UPMC (Paris VI), the Fondation Ophtalmologique A. de Rothschild (Paris), Agence Nationale pour la Recherche (MEDINAS project, ANR-07-TECSAN-014), Fondation Fighting Blindness, Fondation pour la Recherche Médicale, the sixth European framework (DREAMS, project FP6-NMP-2006-676033345; NEUROCARE, project FP7-NMP-280433), IMPLANTS project from ITMO-TecSan, Fédération des Aveugles de France, IRRP, the city of Paris, the Regional Council of Ile-de-France. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.