Literature DB >> 3198798

Localization of putative GABAergic neurons in the larval tiger salamander retina by immunocytochemical and autoradiographic methods.

C Y Yang1, S Yazulla.   

Abstract

Putative GABAergic neurons in the larval tiger salamander retina were localized by a comparative analysis of glutamate decarboxylase immunoreactivity (GAD-IR), GABA-like immunoreactivity (GABA-IR), and high-affinity 3H-GABA uptake at the light microscopical level. Preliminary data showed that all GAD-IR neurons were double labeled for GABA-IR. However, because the weak somatic labeling with GAD-IR, we could not determine if the converse were true. Neurons commonly labeled with GABA-IR and 3H-GABA uptake include horizontal cells, type I (outer) and type II (inner) bipolar cells, type I (inner) and type II (outer) amacrine cells, and cell bodies in the ganglion cell layer (GCL). In addition, interplexiform cells were identified with GABA-IR. The presence of GABA-IR ganglion cells was indicated by GABA-IR fibers in the optic fiber layer and optic nerve as well as by a GABA-IR cell in the GCL that included a labeled axon. The percentage of labeled somas in the inner nuclear layer (INL) compared to all cells in each layer was similar for the two methods: 30% in INL 1 (outer layer of somas), 15% in INL 2 (middle layer), 43-52% in INL 3 (inner layer), and about 21-26% in the GCL. Labeled processes were found in three bands in the inner plexiform layer, with the densest band located in the most proximal part. Postembedding labeling of 1-micron Durcupan resin sections for GABA-IR showed the same general pattern as obtained with 10-microns cryostat sections, with additional staining, however, of type II (inner) bipolar cell Landolt's clubs. Extensive colocalization of labeling was indicated, and we conclude that GABA-IR can serve as a valid and reliable marker for GABA-containing neurons in this retina and suggest that GABA serves as a transmitter for horizontal cells, several types of amacrine cell, a type of interplexiform cell, and perhaps a small percentage of type I and type II bipolar cells and ganglion cells.

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Year:  1988        PMID: 3198798     DOI: 10.1002/cne.902770107

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


  7 in total

1.  Non-linear, high-gain and sustained-to-transient signal transmission from rods to amacrine cells in dark-adapted retina of Ambystoma.

Authors:  Xiong-Li Yang; Fan Gao; Samuel M Wu
Journal:  J Physiol       Date:  2002-02-15       Impact factor: 5.182

2.  Survey on amacrine cells coupling to retrograde-identified ganglion cells in the mouse retina.

Authors:  Ji-Jie Pang; David L Paul; Samuel M Wu
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-08-01       Impact factor: 4.799

3.  Two types of glutamate receptors differentially excite amacrine cells in the tiger salamander retina.

Authors:  D B Dixon; D R Copenhagen
Journal:  J Physiol       Date:  1992-04       Impact factor: 5.182

4.  Taurine, amino acid transmitters, and related molecules in the retina of the Australian lungfish Neoceratodus forsteri: a light-microscopic immunocytochemical and electron-microscopic study.

Authors:  D V Pow
Journal:  Cell Tissue Res       Date:  1994-11       Impact factor: 5.249

Review 5.  Ionotropic GABA Receptors and Distal Retinal ON and OFF Responses.

Authors:  E Popova
Journal:  Scientifica (Cairo)       Date:  2014-07-20

Review 6.  What the salamander eye has been telling the vision scientist's brain.

Authors:  Fernando Rozenblit; Tim Gollisch
Journal:  Semin Cell Dev Biol       Date:  2020-04-29       Impact factor: 7.727

7.  Cone and rod cells have different target preferences in vitro as revealed by optical tweezers.

Authors:  Robert J Clarke; Kormákur Högnason; Michael Brimacombe; Ellen Townes-Anderson
Journal:  Mol Vis       Date:  2008-04-21       Impact factor: 2.367

  7 in total

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