Literature DB >> 1683878

Amacrine cells in the tiger salamander retina: morphology, physiology, and neurotransmitter identification.

C Y Yang1, P Lukasiewicz, G Maguire, F S Werblin, S Yazulla.   

Abstract

Amacrine cells of the vertebrate retina comprise multiple neurochemical types. Yet details of their electrophysiological and morphology properties as they relate to neurotransmitter content are limited. This issue of relating light responsiveness, dendritic projection, and neurotransmitter content has been addressed in the retinal slice preparation of the tiger salamander. Amacrine cells were whole-cell clamped and stained with Lucifer yellow (LY), then processed to determine their immunoreactivity (IR) to GABA, glycine, dopamine or tyrosine hydroxylase (TOH), and glucagon antisera. Widefield, ON-OFF amacrine cells were glycine-IR. The processes of these cells extended laterally in the inner plexiform layer (IPL) from 250-600 microns. They were either multistratified in the IPL or monostratified near the IPL midline. Three multistratified ON-OFF narrowfield glycine-IR cells also were found. Four types of ON amacrine cells were found to be GABA-IR; all types had their processes concentrated in the proximal IPL (sublamina b). Type I cells were narrowfield (approximately 100 microns) with a compact projection. Type II cells were widefield (220-300 microns) with a sparse projection. Type III cells had an asymmetrical projection and varicose processes. Type IV cells were pyriform and monostratified in sublamina b. One narrowfield ON-OFF amacrine cell, with processes broadly distributed in the middle of the IPL, was GABA-IR. This cell appeared similar to an ON-OFF cell that was glycine-IR and may comprise a type in which GABA and glycine colocalize. Another class of amacrine cell, with processes forming a major plexus along the distal border of the IPL and a lesser plexus in the proximal IPL, produced slow responses at light ON and OFF; these cells were dopamine/TOH-IR. A narrowfield class of transient ON-OFF amacrine cell, with processes ramifying throughout both sublaminae a and b of the IPL, were glucagon-IR; these cells appeared to be dye-coupled at the soma. We have shown that, with respect to GABA, glycine, dopamine, and glucagon, salamander amacrine cells fall into rather discrete groups on the basis of ramification patterns in the IPL and responses to photic stimulation. The physiological, structural, and neurochemical diversity of amacrine cells is indicative of multiple and complex roles in retinal processing.

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Year:  1991        PMID: 1683878     DOI: 10.1002/cne.903120103

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


  18 in total

1.  Spatial heterogeneity and function of voltage- and ligand-gated ion channels in retinal amacrine neurons.

Authors:  G Maguire
Journal:  Proc Biol Sci       Date:  1999-05-22       Impact factor: 5.349

2.  Three levels of lateral inhibition: A space-time study of the retina of the tiger salamander.

Authors:  B Roska; E Nemeth; L Orzo; F S Werblin
Journal:  J Neurosci       Date:  2000-03-01       Impact factor: 6.167

3.  Membrane properties of an unusual intrinsically oscillating, wide-field teleost retinal amacrine cell.

Authors:  Eduardo Solessio; Jozsef Vigh; Nicolas Cuenca; Kevin Rapp; Eric M Lasater
Journal:  J Physiol       Date:  2002-11-01       Impact factor: 5.182

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.  GABA(A), GABA(C) and glycine receptor-mediated inhibition differentially affects light-evoked signalling from mouse retinal rod bipolar cells.

Authors:  Erika D Eggers; Peter D Lukasiewicz
Journal:  J Physiol       Date:  2006-01-26       Impact factor: 5.182

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

Authors:  Xin Chen; Hain-Ann Hsueh; Kenneth Greenberg; Frank S Werblin
Journal:  J Neurophysiol       Date:  2010-03-10       Impact factor: 2.714

Review 7.  Colocalization of amino acid signal molecules in neurons and endocrine cells.

Authors:  S Davanger
Journal:  Anat Embryol (Berl)       Date:  1996-07

8.  Response to change is facilitated by a three-neuron disinhibitory pathway in the tiger salamander retina.

Authors:  B Roska; E Nemeth; F S Werblin
Journal:  J Neurosci       Date:  1998-05-01       Impact factor: 6.167

9.  Nonlinear spatial integration in the receptive field surround of retinal ganglion cells.

Authors:  Daisuke Takeshita; Tim Gollisch
Journal:  J Neurosci       Date:  2014-05-28       Impact factor: 6.167

10.  Adaptation of Inhibition Mediates Retinal Sensitization.

Authors:  David B Kastner; Yusuf Ozuysal; Georgia Panagiotakos; Stephen A Baccus
Journal:  Curr Biol       Date:  2019-08-01       Impact factor: 10.834

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