• DocumentCode
    933735
  • Title

    Neuronal Network Morphology and Electrophysiologyof Hippocampal Neurons Cultured on Surface-Treated Multielectrode Arrays

  • Author

    Soussou, Walid V. ; Yoon, Geoffrey J. ; Brinton, Roberta Diaz ; Berger, Theodore W.

  • Author_Institution
    Univ. of Southern California, Los Angeles
  • Volume
    54
  • Issue
    7
  • fYear
    2007
  • fDate
    7/1/2007 12:00:00 AM
  • Firstpage
    1309
  • Lastpage
    1320
  • Abstract
    Toward the development of biocompatible surfaces for implantable electrode arrays and the creation of patterned neuronal networks, the impact of select biochemical substrates [poly-D-lysine (PDL), polyornithine (PO), polyethylenimine (PEI), and a basement membrane extract (BM)] on network morphology and spontaneous electrophysiological activity of dissociated hippocampal neurons was investigated. Cultured in serum-free Neurobasal medium at 100 000 cells/cm2, neurons attached to each substrate. PDL, PO, and PEI induced little or no neuronal clustering and process fasciculation, whereas the addition of BM promoted these features. The ratios of somas to processes, and axons to dendrites, as determined by immunohistochemical staining and image analysis were comparable across all substrates. Spontaneous firing was recorded using planar multielectrode arrays (MEAs) at the third week in vitro for the two most divergent morphologies according to Euclidian cluster analysis, namely those induced by PO + BM and PEI. Mean spike amplitude, mean firing rate, median interspike interval (ISI), mean burst rate, and correlation index were analyzed and compared to morphological features. Synchronized bursting was highly correlated with neuronal clustering and process fasciculation. Spike amplitude was negatively correlated with thin branching which was most evident in neurons grown on PEI. These data indicate that factors, which influence adherence of neurons to surfaces, can profoundly impact both neuronal network morphology and electrophysiological activity in vitro.
  • Keywords
    biochemistry; bioelectric phenomena; biomedical electrodes; biomedical optical imaging; biomembranes; brain; cellular biophysics; molecular biophysics; neurophysiology; polymer films; Euclidian cluster analysis; axons; basement membrane extract; biochemical substrates; biocompatible surfaces; burst rate; correlation index; dendrites; electrophysiology; hippocampal neurons; image analysis; immunohistochemical staining; implantable electrode arrays; interspike interval; neuronal clustering; neuronal network morphology; planar multielectrode arrays; poly-D-lysine; polyethylenimine; polyornithine; process fasciculation; serum-free Neurobasal medium; somas; spontaneous firing; surface-treated multielectrode arrays; Biological neural networks; Biomembranes; Cells (biology); Electrodes; Electrophysiology; In vitro; Nerve fibers; Neurons; Page description languages; Surface morphology; Basement membrane; multielectrode array; neuronal network morphology; spontaneous electrophysiological activity; Action Potentials; Animals; Cell Adhesion; Cell Culture Techniques; Cells, Cultured; Electrophysiology; Equipment Design; Equipment Failure Analysis; Female; Hippocampus; Microelectrodes; Nerve Net; Neurons; Rats; Rats, Sprague-Dawley;
  • fLanguage
    English
  • Journal_Title
    Biomedical Engineering, IEEE Transactions on
  • Publisher
    ieee
  • ISSN
    0018-9294
  • Type

    jour

  • DOI
    10.1109/TBME.2006.889195
  • Filename
    4237350