July 2019
Volume 60, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2019
Multi-Electrode-Recording for classification of retinal ganglion cells for bionic vision: comparison with calcium imaging responses.
Author Affiliations & Notes
  • hamed shabani
    Institute for Ophthalmic Research, University of Tuebingen, Tuebingen, Germany
  • Mahdi Sadeghi
    University of Tuebingen, Germany
  • Zohreh Hosseinzadeh
    University of Tuebingen, Germany
  • Eberhart Zrenner
    Institute for Ophthalmic Research, University of Tuebingen, Tuebingen, Germany
  • Daniel Llewellyn Rathbun
    Institute for Ophthalmic Research, University of Tuebingen, Tuebingen, Germany
  • Footnotes
    Commercial Relationships   hamed shabani, None; Mahdi Sadeghi, None; Zohreh Hosseinzadeh, None; Eberhart Zrenner, Retina Implant AG, Reutlingen (F), Retina Implant AG, Reutlingen (I), Retina Implant AG, Reutlingen (C), Retina Implant AG, Reutlingen (P), Retina Implant AG, Reutlingen (R), Retina Implant AG, Reutlingen (S); Daniel Rathbun, None
  • Footnotes
    Support  German Federal Ministry of Education and Research (BMBF)
Investigative Ophthalmology & Visual Science July 2019, Vol.60, 5283. doi:
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      hamed shabani, Mahdi Sadeghi, Zohreh Hosseinzadeh, Eberhart Zrenner, Daniel Llewellyn Rathbun; Multi-Electrode-Recording for classification of retinal ganglion cells for bionic vision: comparison with calcium imaging responses.. Invest. Ophthalmol. Vis. Sci. 2019;60(9):5283.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : We hypothesize that different types of RGCs can be selectively activated by deriving stimuli from their different electrical input filters. The input filters of cells are extracted from their response to electrical noise stimulation using the Spike Triggered Averaging (STA) method. To begin testing this hypothesis, we first classify RGC types using a set of visual stimuli and then examine the properties of each cell type’s electrical input filters.

Methods : In this study we used the data recorded from seven dark adapted retinas of six adult wild type mice. A 60 channel microelectrode array in contact with the ganglion cell side of the retina was used to record the spiking neural activity of RGCs. The visual stimulation set was adapted from Baden et al. (Nature 2016), including moving bars, contrast and temporal frequency chirps, blue-green color flashes, and spatiotemporal white noise. In order to extract electrical input filters, a sequence of filtered and interpolated Gaussian white noise voltage steps was used. Similar to Baden et al. we used sparse principle component analysis (sPCA) to extract response features to the visual stimuli.
After projecting data into a lower-dimensional space, we assigned each neuron to one of the 75 clusters reported by Baden et al., by finding the highest correlation between a neuron’s response and the clustered response data provided by Baden et al.

Results : We recorded visual responses from 155 RGCs. These responses mapped onto about half of the previously described clusters. Despite convolving our spike trains with a filter to create pseudo-calcium traces for correlation with the previous dataset, many of our responses were significantly more transient than previously reported. ON and OFF cells had different electrical input filters as we have previously reported.

Conclusions : Adaptation of the Baden et al. methodology for spike trains instead of calcium recordings was partially successful. For better classification results, new cluster definitions should be derived from a large spike train data set. Electrical input filters do appear to vary with RGC type, but more precise cluster definitions are needed to refine this result.

This abstract was presented at the 2019 ARVO Annual Meeting, held in Vancouver, Canada, April 28 - May 2, 2019.

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