scholarly journals Axonal Transmission in the Retina Introduces a Small Dispersion of Relative Timing in the Ganglion Cell Population Response

PLoS ONE ◽  
2011 ◽  
Vol 6 (6) ◽  
pp. e20810 ◽  
Author(s):  
Günther Zeck ◽  
Armin Lambacher ◽  
Peter Fromherz
Keyword(s):  
Ganglion Cell ◽  
Cell Population ◽  
Relative Timing ◽  
Population Response ◽  
Small Dispersion

scholarly journals A cell population model of retinal ganglion cell layer thickness

2019 ◽  
Vol 19 (10) ◽  
pp. 41c
Author(s):  
Kara N Cloud ◽  
Min Chen ◽  
Jessica I. W. Morgan ◽  
Geoffrey K. Aguirre
Keyword(s):  
Ganglion Cell ◽  
Layer Thickness ◽  
Retinal Ganglion Cell ◽  
Cell Population ◽  
Population Model ◽  
Ganglion Cell Layer ◽  
Cell Layer ◽  
Retinal Ganglion ◽  
Retinal Ganglion Cell Layer ◽  
A Cell

Ganglion cells influence the fate of dividing retinal cells in culture

Development ◽  
1998 ◽  
Vol 125 (6) ◽  
pp. 1059-1066 ◽  
Author(s):  
D.K. Waid ◽  
S.C. McLoon
Keyword(s):  
Ganglion Cell ◽  
Cell Fate ◽  
Cell Population ◽  
Antisense Oligonucleotide ◽  
Ganglion Cells ◽  
Cell Types ◽  
Retinal Cell ◽  
Retinal Cells ◽  
Cell Production ◽  
Cellular Environment

The different retinal cell types arise during vertebrate development from a common pool of progenitor cells. The mechanisms responsible for determining the fate of individual retinal cells are, as yet, poorly understood. Ganglion cells are one of the first cell types to be produced in the developing vertebrate retina and few ganglion cells are produced late in development. It is possible that, as the retina matures, the cellular environment changes such that it is not conducive to ganglion cell determination. The present study showed that older retinal cells secrete a factor that inhibits the production of ganglion cells. This was shown by culturing younger retinal cells, the test population, adjacent to various ages of older retinal cells. Increasingly older retinal cells, up to embryonic day 9, were more effective at inhibiting production of ganglion cells in the test cell population. Ganglion cell production was restored when ganglion cells were depleted from the older cell population. This suggests that ganglion cells secrete a factor that actively prevents cells from choosing the ganglion cell fate. This factor appeared to be active in medium conditioned by older retinal cells. Analysis of the conditioned medium established that the factor was heat stable and was present in the <3 kDa and >10 kDa fractions. Previous work showed that the neurogenic protein, Notch, might also be active in blocking production of ganglion cells. The present study showed that decreasing Notch expression with an antisense oligonucleotide increased the number of ganglion cells produced in a population of young retinal cells. Ganglion cell production, however, was still inhibited in cultures using antisense oligonucleotide to Notch in medium conditioned by older retinal cells. This suggests that the factor secreted by older retinal cells inhibits ganglion cell production through a different pathway than that mediated by Notch.

S240 – Human Cochlear Implant Histopathology

2008 ◽  
Vol 139 (2_suppl) ◽  
pp. P155-P155
Author(s):  
Helen Xu ◽  
Natasha Pollak ◽  
Sebahattin Cureoglu ◽  
Michael M Paparella
Keyword(s):  
Cochlear Implant ◽  
Ganglion Cell ◽  
Cell Population ◽  
Ganglion Cells ◽  
Clinical Performance ◽  
Spiral Ganglion ◽  
Spiral Ganglion Cell ◽  
Cell Counts ◽  
Temporal Bones ◽  
Normal Spiral

Objectives 1) To exam the histopathology of multichannel cochlear implant temporal bones. 2) To evaluate the relationship of residual spiral ganglion cell counts to clinical hearing performance. Methods 8 temporal bones from 4 cochlear implant patients were examined histologically. Paired comparisons were made between implanted and nonimplanted temporal bones. Clinical performance data was obtained from patient charts. Results There were varying amounts of inflammation (fibrosis and ossification) in the basal turn of the cochlear in all implanted temporal bones. Trauma to the facial nerve at facial recess site was noticed in 1 case. Compared with nonimplanted ears, 2 implanted bones with less than 10-year duration of implantation had no significant changes of spiral ganglion cell population. One case with prolong implant duration (15 years) showed about 36% decrease of spiral ganglion cells at the implanted site. The case with best speech recognition (89% with CID sentence) had the highest residual spiral ganglion cells (30% of normal spiral ganglion cell population). 2 cases with poor clinical performance (< 10% with CID sentence) had the residual spiral ganglion cells at 11% and 22%. The case with moderate clinical performance (30% with CID sentence) had 14% of normal spiral ganglion cell population. Surviving dendrites varied from 5% to 30% among 4 cases with no relationship to clinical performance. Conclusions Our findings suggest prolonged implantation may affect spiral ganglion cell population. There is no reverse relationship between residual spiral ganglion cells in implanted temporal bones to clinical speech performance observed from our limited cases.

scholarly journals Representations of the amacrine cell population underlying retinal motion anticipation

2019 ◽  
Author(s):  
Michael D. Menz ◽  
Dongsoo Lee ◽  
Stephen A. Baccus
Keyword(s):  
Ganglion Cell ◽  
Cell Population ◽  
Amacrine Cell ◽  
Ganglion Cells ◽  
Computational Modelling ◽  
Amacrine Cells ◽  
Cell Populations ◽  
Population Activity ◽  
General Role ◽  
Moving Stimuli

AbstractRetinal amacrine cells are a diverse population of inhibitory interneurons, posing a challenge to understand the specific roles of those interneurons in computations of the similarly diverse ganglion cell population. Here we study the predictive computation of motion anticipation, which is thought to compensate for processing delays when encoding moving objects. We recorded the membrane potential of the salamander amacrine cell population optically while recording electrically from ganglion cells with a multielectrode array. We find unexpectedly that ganglion cells with the greatest anticipation for moving stimuli exhibit a new type of predictive motion anticipation that is inconsistent with prior models of delayed inhibition. Based on the spatiotemporal correlations between thousands of amacrine and ganglion cell pairs, we modeled the contribution of the traveling wave of activity for different amacrine cell populations to the encoding of a moving bar. These models indicate that the population responses of slow biphasic amacrine cells create the greatest contribution to both types of ganglion cell motion anticipation, supporting a role for this specific amacrine cell class in the predictive encoding of moving stimuli.Significance StatementThe prediction of moving stimuli is a widespread function occurring in both visual and auditory systems. The diversity of interneuron populations makes it a challenge to understand the mechanisms of these computations. To analyze how the retina anticipates motion, we optically measured inhibitory amacrine cell population activity simultaneously with electrical recording from ganglion cell populations. We then used computational modelling to assess which amacrine cell types have the right spatiotemporal responses to generate motion anticipation. In contrast to previous suggestions of a general role for inhibition, we find that slow biphasic amacrine cells specifically have the greatest contribution to motion anticipation, thus highlighting the need to directly measure and model the effects of interneuron populations in complex sensory computations.

Lack of early pattern stimulation prevents normal development of the alpha (Y) retinal ganglion cell population in the cat

2012 ◽  
Vol 520 (11) ◽  
pp. 2414-2429 ◽  
Author(s):  
Kalina Burnat ◽  
Estelle Van Der Gucht ◽  
Wioletta J. Waleszczyk ◽  
Malgorzata Kossut ◽  
Lutgarde Arckens
Keyword(s):  
Ganglion Cell ◽  
Retinal Ganglion Cell ◽  
Cell Population ◽  
Normal Development ◽  
Retinal Ganglion ◽  
Pattern Stimulation

Changes in human short-wavelength-sensitive and achromatic resolution acuity with retinal eccentricity and meridian

2005 ◽  
Vol 22 (1) ◽  
pp. 79-86 ◽  
Author(s):  
RAYMOND O. BEIRNE ◽  
MARGARITA B. ZLATKOVA ◽  
ROGER S. ANDERSON
Keyword(s):  
Visual Field ◽  
Population Density ◽  
Ganglion Cell ◽  
Cell Density ◽  
Cell Population ◽  
Short Wavelength ◽  
Peripheral Vision ◽  
Retinal Eccentricity ◽  
Horizontal Meridian ◽  
Predicted Values

Psychophysical measurements using achromatic grating resolution acuity in peripheral vision show a prominent retinal asymmetry in acuity which is consistent with predicted values based on available estimates of midget ganglion cell density. Recent studies have shown that peripheral grating resolution acuity values for short-wavelength-sensitive (SWS) isolating gratings in normal observers are closely related to predicted values based on the underlying small bistratified ganglion cell density. By measuring SWS resolution acuity at different locations across the visual field, we wished to see if any significant acuity asymmetry exists for the short-wavelength system. In addition to this, we wanted to compare SWS and achromatic resolution acuity at different retinal locations of equal eccentricity. SWS and achromatic grating resolution acuity was measured in two observers at a number of different retinal meridians of 10- and 25-deg eccentricity from the fovea, and out to 35-deg eccentricity along the horizontal meridian. Achromatic resolution acuity was higher than SWS resolution acuity at all locations. At 10-deg eccentricity there was slight radial asymmetry in SWS and achromatic acuity, both displaying highest acuity along the horizontal meridian. At 25-deg eccentricity, SWS and achromatic acuity showed significant asymmetry with acuity being higher in the nasal retina compared to the temporal retina and with higher acuity in the superior retina compared to the inferior retina. At 35-deg eccentricity, the acuity asymmetry along the horizontal meridian was maintained with acuity for both significantly higher in the nasal retina. The SWS acuity changes with eccentricity and meridian were qualitatively similar to that found for achromatic acuity at the majority of retinal locations. Like achromatic acuity, SWS acuity shows significant asymmetry at different retinal locations of equal eccentricity. This suggests that both the midget and small bistratified ganglion cell population density changes significantly with retinal location and eccentricity. SWS acuity appears to change in parallel with achromatic acuity for the majority of retinal locations measured, although the amount of nasotemporal asymmetry appears to be slightly less for the SWS system at 25- and 35-deg eccentricity.

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