Literature DB >> 12385625

Coupling pattern of S1 and S2 amacrine cells in the rabbit retina.

Wei Li1, Jian Zhang, Stephen C Massey.   

Abstract

Previous studies have shown that indoleamine-accumulating cells (IACs) in the rabbit retina consist of two main cell types: S1 and S2 amacrine cells (Vaney, 1986; Sandell & Masland, 1986). Both cell types are wide-field GABA amacrine cells that make reciprocal synaptic contacts with rod bipolar cell terminals (Ehinger & Holmgren, 1979; Strettoi et al., 1990). We have examined the coupling pattern of S1 and S2 amacrine cells after the intracellular injection of Neurobiotin. Our results may be summarized as follows: (1) S1 amacrine cells were extensively coupled and their dendrites formed a network similar to but less dense than the matrix stained with an antibody to serotonin. (2) Morphological observations and cluster analysis, based on a scattergram, showed that the vast majority of coupled cells were S1 amacrine cells, accounting for approximately half of the total IACs. The rest of the uncoupled IACs were S2 amacrine cells. (3) Sometimes, two adjacent varicosities, one from an injected S1 and one from a coupled S1, contacted a single rod bipolar terminal. (4) S2 amacrine cells were also coupled but much less than the S1s. (5) Rarely, crossover coupling between S1 and S2 amacrine cells was observed. These results suggest that the extensive coupling between S1 amacrine cells, combined with a larger dendritic field, may contribute a wide-field component to the inhibitory surround of the rod pathway. By comparison, the smaller, weakly coupled S2 amacrine cells may provide a local component.

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Year:  2002        PMID: 12385625     DOI: 10.1017/s0952523802191115

Source DB:  PubMed          Journal:  Vis Neurosci        ISSN: 0952-5238            Impact factor:   3.241


  10 in total

1.  Differential output of the high-sensitivity rod photoreceptor: AII amacrine pathway.

Authors:  Artemis Petrides; E Brady Trexler
Journal:  J Comp Neurol       Date:  2008-04-10       Impact factor: 3.215

2.  Wide-field diffuse amacrine cells in the monkey retina contain immunoreactive Cocaine- and Amphetamine-Regulated Transcript (CART).

Authors:  Ye Long; Andrea S Bordt; Weiley S Liu; Elizabeth P Davis; Stephen J Lee; Luke Tseng; Alice Z Chuang; Christopher M Whitaker; Stephen C Massey; Michael B Sherman; David W Marshak
Journal:  Peptides       Date:  2016-08-25       Impact factor: 3.750

3.  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

4.  Parvalbumin-immunoreactive amacrine cells of macaque retina.

Authors:  Kathryn E Klump; Ai-Jun Zhang; Samuel M Wu; David W Marshak
Journal:  Vis Neurosci       Date:  2009-05-13       Impact factor: 3.241

5.  Functional NMDA receptors are expressed by both AII and A17 amacrine cells in the rod pathway of the mammalian retina.

Authors:  Yifan Zhou; Barbora Tencerová; Espen Hartveit; Margaret L Veruki
Journal:  J Neurophysiol       Date:  2015-11-11       Impact factor: 2.714

6.  Single-photon absorptions evoke synaptic depression in the retina to extend the operational range of rod vision.

Authors:  Felice A Dunn; Fred Rieke
Journal:  Neuron       Date:  2008-03-27       Impact factor: 17.173

7.  The Usher gene cadherin 23 is expressed in the zebrafish brain and a subset of retinal amacrine cells.

Authors:  Greta Glover; Kaspar P Mueller; Christian Söllner; Stephan C F Neuhauss; Teresa Nicolson
Journal:  Mol Vis       Date:  2012-09-05       Impact factor: 2.367

8.  Electrical coupling between A17 cells enhances reciprocal inhibitory feedback to rod bipolar cells.

Authors:  Claudio Elgueta; Felix Leroy; Alex H Vielma; Oliver Schmachtenberg; Adrian G Palacios
Journal:  Sci Rep       Date:  2018-02-15       Impact factor: 4.379

9.  A computational framework for ultrastructural mapping of neural circuitry.

Authors:  James R Anderson; Bryan W Jones; Jia-Hui Yang; Marguerite V Shaw; Carl B Watt; Pavel Koshevoy; Joel Spaltenstein; Elizabeth Jurrus; Kannan U V; Ross T Whitaker; David Mastronarde; Tolga Tasdizen; Robert E Marc
Journal:  PLoS Biol       Date:  2009-03-31       Impact factor: 8.029

10.  Rod-cone crossover connectome of mammalian bipolar cells.

Authors:  J Scott Lauritzen; Crystal L Sigulinsky; James R Anderson; Michael Kalloniatis; Noah T Nelson; Daniel P Emrich; Christopher Rapp; Nicholas McCarthy; Ethan Kerzner; Miriah Meyer; Bryan W Jones; Robert E Marc
Journal:  J Comp Neurol       Date:  2016-08-23       Impact factor: 3.215

  10 in total

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