Literature DB >> 20220071

Three forms of spatial temporal feedforward inhibition are common to different ganglion cell types in rabbit retina.

Xin Chen1, Hain-Ann Hsueh, Kenneth Greenberg, Frank S Werblin.   

Abstract

There exist more than 30 different morphological amacrine cell types, but there may be fewer physiological types. Here we studied the amacrine cell outputs by measuring the temporal and spatial properties of feedforward inhibition to four different types of ganglion cells. These ganglion cells, each with concentric receptive field organization, appear to receive a different relative contribution of the same three forms of feed-forward inhibition, namely: local glycinergic, local sustained GABAergic, and broad transient GABAergic inhibition. Two of these inhibitory components, local glycinergic inhibition and local sustained GABAergic inhibition were localized to narrow regions confined to the dendritic fields of the ganglion cells. The third, a broad transient GABAergic inhibition, was driven from regions peripheral to the dendritic area. Each inhibitory component is also correlated with characteristic kinetics expressed in all ganglion cells: broad transient GABAergic inhibition had the shortest latency, local glycinergic inhibition had an intermediate latency, and local sustained GABAergic inhibition had the longest latency. We suggest each of these three inhibitory components represents the output from a distinct class of amacrine cell, mediates a specific visual function, and each forms a basic functional component for the four ganglion cell types. Similar subunits likely exist in the circuits of other ganglion cell types as well.

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Year:  2010        PMID: 20220071      PMCID: PMC4073908          DOI: 10.1152/jn.01109.2009

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  56 in total

1.  The shapes and numbers of amacrine cells: matching of photofilled with Golgi-stained cells in the rabbit retina and comparison with other mammalian species.

Authors:  M A MacNeil; J K Heussy; R F Dacheux; E Raviola; R H Masland
Journal:  J Comp Neurol       Date:  1999-10-18       Impact factor: 3.215

2.  Lateral inhibition in the inner retina is important for spatial tuning of ganglion cells.

Authors:  P B Cook; J S McReynolds
Journal:  Nat Neurosci       Date:  1998-12       Impact factor: 24.884

3.  RECEPTIVE FIELDS OF RABBIT RETINAL GANGLION CELLS.

Authors:  W R LEVICK
Journal:  Am J Optom Arch Am Acad Optom       Date:  1965-06

4.  Inner and outer retinal pathways both contribute to surround inhibition of salamander ganglion cells.

Authors:  Tomomi Ichinose; Peter D Lukasiewicz
Journal:  J Physiol       Date:  2005-03-10       Impact factor: 5.182

5.  Directional selectivity is formed at multiple levels by laterally offset inhibition in the rabbit retina.

Authors:  Shelley I Fried; Thomas A Münch; Frank S Werblin
Journal:  Neuron       Date:  2005-04-07       Impact factor: 17.173

6.  Parallel processing in retinal ganglion cells: how integration of space-time patterns of excitation and inhibition form the spiking output.

Authors:  Botond Roska; Alyosha Molnar; Frank S Werblin
Journal:  J Neurophysiol       Date:  2006-03-01       Impact factor: 2.714

7.  Extreme diversity among amacrine cells: implications for function.

Authors:  M A MacNeil; R H Masland
Journal:  Neuron       Date:  1998-05       Impact factor: 17.173

8.  TTX attenuates surround inhibition in rabbit retinal ganglion cells.

Authors:  W R Taylor
Journal:  Vis Neurosci       Date:  1999 Mar-Apr       Impact factor: 3.241

9.  Quantitative analysis of neuronal morphologies in the mouse retina visualized by using a genetically directed reporter.

Authors:  Tudor Constantin Badea; Jeremy Nathans
Journal:  J Comp Neurol       Date:  2004-12-20       Impact factor: 3.215

10.  Glycinergic amacrine cells of the rat retina.

Authors:  N Menger; D V Pow; H Wässle
Journal:  J Comp Neurol       Date:  1998-11-09       Impact factor: 3.215

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  20 in total

1.  Harmonic analysis of the cone flicker ERG of rabbit.

Authors:  Haohua Qian; Kenneth R Alexander; Harris Ripps
Journal:  Exp Eye Res       Date:  2010-10-23       Impact factor: 3.467

2.  Cell populations of the retina: the Proctor lecture.

Authors:  Richard H Masland
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-06-28       Impact factor: 4.799

Review 3.  GABAergic neurotransmission and retinal ganglion cell function.

Authors:  E Popova
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2015-02-06       Impact factor: 1.836

4.  Inhibitory mechanisms that generate centre and surround properties in ON and OFF brisk-sustained ganglion cells in the rabbit retina.

Authors:  Ilya Buldyrev; W Rowland Taylor
Journal:  J Physiol       Date:  2012-10-08       Impact factor: 5.182

5.  Selective glycine receptor α2 subunit control of crossover inhibition between the on and off retinal pathways.

Authors:  Regina D Nobles; Chi Zhang; Ulrike Müller; Heinrich Betz; Maureen A McCall
Journal:  J Neurosci       Date:  2012-03-07       Impact factor: 6.167

6.  Adeno-associated virus-RNAi of GlyRα1 and characterization of its synapse-specific inhibition in OFF alpha transient retinal ganglion cells.

Authors:  C Zhang; S B Rompani; B Roska; M A McCall
Journal:  J Neurophysiol       Date:  2014-09-17       Impact factor: 2.714

7.  Two transcription factors, Pou4f2 and Isl1, are sufficient to specify the retinal ganglion cell fate.

Authors:  Fuguo Wu; Tadeusz J Kaczynski; Santhosh Sethuramanujam; Renzhong Li; Varsha Jain; Malcolm Slaughter; Xiuqian Mu
Journal:  Proc Natl Acad Sci U S A       Date:  2015-03-16       Impact factor: 11.205

8.  Properties of the ON bistratified ganglion cell in the rabbit retina.

Authors:  Hideo Hoshi; Lian-Ming Tian; Stephen C Massey; Stephen L Mills
Journal:  J Comp Neurol       Date:  2013-05-01       Impact factor: 3.215

Review 9.  Receptor targets of amacrine cells.

Authors:  Chi Zhang; Maureen A McCall
Journal:  Vis Neurosci       Date:  2012-01       Impact factor: 3.241

10.  GlyRα2, not GlyRα3, modulates the receptive field surround of OFF retinal ganglion cells.

Authors:  Chi Zhang; Regina D Nobles; Maureen A McCall
Journal:  Vis Neurosci       Date:  2015       Impact factor: 3.241

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