Literature DB >> 9548552

Gamma-aminobutyric acidA receptors on a bistratified amacrine cell type in the rabbit retina.

C L Zucker1, B Ehinger.   

Abstract

Gamma-Aminobutyric acid (GABA) is considered to be a major inhibitory neurotransmitter in the inner plexiform layer of the retinas of all vertebrate species. It is contained in and released from nearly 40% of the amacrine cells and is known to play a major role in many aspects of visual processing. By using well-characterized antibodies to several subunits of the GABA(A) receptor, we have analyzed their localization on the cell bodies and dendritic trees of two amacrine cell populations in the rabbit retina, which have been either filled intracellularly with Lucifer yellow or stained immunohistochemically. Both populations are selectively stained by intravitreal injection of the fluorescent nuclear dye 4',6-diaminidin-2-phenylindoldihydrochloride (DAPI). We have found that the most significant concentration of the alpha1 and beta2/3 GABA(A) receptor subunits is localized to the DAPI-3 type amacrine cell. The perikarya of the DAPI-3 cells are found in the proximal inner nuclear layer and send their processes into two sublayers in sublaminae a and b of the inner plexiform layer. These processes abut but do not directly overlap those of the two mirror-symmetric populations of starburst amacrine cells. Because the cell bodies of the DAPI-3 cells are the only ones in the inner nuclear layer that stain strongly for either the alpha1 or beta2/3 subunits, such staining is a diagnostic feature of these cells. Their processes also constitute the most strongly staining ones found within the inner plexiform layer. The dendritic trees of DAPI-3 cells, which range from about 150 microm up to about 300 microm, exhibit recurvate looping processes reminiscent of those described for directionally selective ganglion cells. In contrast to the DAPI-3 cell, we have also shown that the starburst amacrine cells exhibit no immunoreactivity for the alpha1 GABA(A) receptor subunit and very little for the beta2/3 subunit. Thus, we have shown that the DAPI-3 cells contain the highest concentrations of the alpha1 and beta2/3 GABA(A) receptor subunits in the rabbit retina. These cells, which costratify near the processes of both the starburst amacrine cells and the ON-OFF directionally selective ganglion cells, thus, are situated both anatomically and by virtue of their receptor content to potentially interact.

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Year:  1998        PMID: 9548552     DOI: 10.1002/(sici)1096-9861(19980413)393:3<309::aid-cne4>3.0.co;2-5

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  6 in total

1.  GABA(A) receptor-mediated signaling alters the structure of spontaneous activity in the developing retina.

Authors:  Chih-Tien Wang; Aaron G Blankenship; Anastasia Anishchenko; Justin Elstrott; Michael Fikhman; Shigetada Nakanishi; Marla B Feller
Journal:  J Neurosci       Date:  2007-08-22       Impact factor: 6.167

Review 2.  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

3.  Nicotinic and muscarinic acetylcholine receptors shape ganglion cell response properties.

Authors:  Christianne E Strang; Ye Long; Konstantin E Gavrikov; Franklin R Amthor; Kent T Keyser
Journal:  J Neurophysiol       Date:  2014-10-08       Impact factor: 2.714

4.  Modeling Starburst cells' GABA(B) receptors and their putative role in motion sensitivity.

Authors:  Norberto M Grzywacz; Charles L Zucker
Journal:  Biophys J       Date:  2006-04-28       Impact factor: 4.033

5.  Compartmental localization of gamma-aminobutyric acid type B receptors in the cholinergic circuitry of the rabbit retina.

Authors:  Charles L Zucker; James E Nilson; Berndt Ehinger; Norberto M Grzywacz
Journal:  J Comp Neurol       Date:  2005-12-19       Impact factor: 3.215

6.  Generation of recombinant antibodies to rat GABAA receptor subunits by affinity selection on synthetic peptides.

Authors:  Sujatha P Koduvayur; Hélène A Gussin; Rajni Parthasarathy; Zengping Hao; Brian K Kay; David R Pepperberg
Journal:  PLoS One       Date:  2014-02-19       Impact factor: 3.240

  6 in total

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