Literature DB >> 7014659

GABAergic amacrine cells in rat retina: immunocytochemical identification and synaptic connectivity.

J E Vaughn, E V Famiglietti, R P Barber, K Saito, E Roberts, C E Ribak.   

Abstract

GABAergic neurons have been identified in light and electron microscopic preparations of rat retina by an immunocytochemical localization of the GABA-synthesizing enzyme, glutamic acid decarboxylase (GAD). GAD-positive neuronal somata are found only in the inner and middle parts of the inner nuclear layer, and GAD-positive neuronal terminals are observed exclusively within the inner plexiform layer (IPL) and the outermost part of the ganglion cell layer. Dense aggregations of GAD-positive terminals alternate with less dense zones to form a lamination of the IPL. GAD-positive terminals contain pleomorphic synaptic vesicles and are the presynaptic elements of conventional synapses onto bipolar and amacrine cell processes, as well as onto the somata and dendrites of ganglion cells. In addition, GAD-positive terminals are postsynaptic to unstained bipolar terminals and are components of synaptic dyads where they occasionally appear to form reciprocal synapses with the bipolar terminals, and serial with unstained amacrine processes. Probable synaptic contacts between adjacent GAD-positive terminals also have been observed. Most of the synaptic input to GAD-positive terminals comes from bipolar cells, while the small remaining input mainly comes from other GAD-positive terminals. The synaptic output to GAD-positive terminals is greatest to bipolar cells, followed in decreasing order by GAD-negative amacrine cells, ganglion cells, and other GAD-positive cells. The total synaptic output of GAD-positive cells appears to be more than twice as great as the total input of these cells. The location of GAD-positive somata, the distribution of GAD-positive terminals, and the synaptic relationships formed by these terminals all indicate that amacrine cells are the only GABAergic neurons in rat retina. Our observations also indicate that not all amacrines are GABAergic and suggest that GABAergic neurons may be limited to a narrow field subclass of amacrine cell. The findings concerning the synaptic connections of GABAergic amacrines suggest that such cells are the first link in several divergent pathways from bipolar to ganglion cells and that they probably serve more than one function since they feed synaptic activity forward directly upon ganglion cells as well as back upon bipolar cells.

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Year:  1981        PMID: 7014659     DOI: 10.1002/cne.901970109

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


  17 in total

1.  The mismatch problem for GABAergic amacrine cells in goldfish retina: resolution and other issues.

Authors:  S Yazulla
Journal:  Neurochem Res       Date:  1991-03       Impact factor: 3.996

2.  Interneuron circuits tune inhibition in retinal bipolar cells.

Authors:  Erika D Eggers; Peter D Lukasiewicz
Journal:  J Neurophysiol       Date:  2009-11-11       Impact factor: 2.714

3.  Dopamine D1 receptor activation contributes to light-adapted changes in retinal inhibition to rod bipolar cells.

Authors:  Michael D Flood; Johnnie M Moore-Dotson; Erika D Eggers
Journal:  J Neurophysiol       Date:  2018-05-30       Impact factor: 2.714

4.  Cellular distribution of L-glutamate decarboxylase (GAD) and gamma-aminobutyric acidA (GABAA) receptor mRNAs in the retina.

Authors:  N C Brecha; C Sternini; M F Humphrey
Journal:  Cell Mol Neurobiol       Date:  1991-10       Impact factor: 5.046

5.  GABA concentration and GAD activity levels in normal and degenerated retinas from mice.

Authors:  T Kato; Y L Murashima
Journal:  Neurochem Res       Date:  1987-06       Impact factor: 3.996

6.  Action and localization of gamma-aminobutyric acid in the cat retina.

Authors:  J Bolz; T Frumkes; T Voigt; H Wässle
Journal:  J Physiol       Date:  1985-05       Impact factor: 5.182

7.  Gamma-aminobutyrate type B receptor modulation of L-type calcium channel current at bipolar cell terminals in the retina of the tiger salamander.

Authors:  G Maguire; B Maple; P Lukasiewicz; F Werblin
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

8.  Expression of GAT-1, a high-affinity gamma-aminobutyric acid plasma membrane transporter in the rat retina.

Authors:  N C Brecha; C Weigmann
Journal:  J Comp Neurol       Date:  1994-07-22       Impact factor: 3.215

9.  Heterogeneous transgene expression in the retinas of the TH-RFP, TH-Cre, TH-BAC-Cre and DAT-Cre mouse lines.

Authors:  H E Vuong; L Pérez de Sevilla Müller; C N Hardi; D G McMahon; N C Brecha
Journal:  Neuroscience       Date:  2015-08-31       Impact factor: 3.590

10.  Catecholaminergic neurons containing GABA-like and/or glutamic acid decarboxylase-like immunoreactivities in various brain regions of the rat.

Authors:  T Kosaka; K Kosaka; Y Hataguchi; I Nagatsu; J Y Wu; O P Ottersen; J Storm-Mathisen; K Hama
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

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