Literature DB >> 3209734

Localization of glycine-containing neurons in the Macaca monkey retina.

A E Hendrickson1, M A Koontz, R G Pourcho, P V Sarthy, D J Goebel.   

Abstract

Autoradiography following 3H-glycine (Gly) uptake and immunocytochemistry with a Gly-specific antiserum were used to identify neurons in Macaca monkey retina that contain a high level of this neurotransmitter. High-affinity uptake of Gly was shown to be sodium dependent whereas release of both endogenous and accumulated Gly was calcium dependent. Neurons labeling for Gly included 40-46% of the amacrine cells and nearly 40% of the bipolars. Synaptic labeling was seen throughout the inner plexiform layer (IPL) but with a preferential distribution in the inner half. Bands of labeled puncta occurred in S2, S4, and S5. Both light and postembedding electron microscopic (EM) immunocytochemistry identified different types of amacrine and bipolar cell bodies and their synaptic terminals. The most heavily labeled Gly+ cell bodies typically were amacrine cells having a single, thick, basal dendrite extending deep into the IPL and, at the EM level, electron-dense cytoplasm and prominent nuclear infoldings. This cell type may be homologous with the Gly2 cell in human retina (Marc and Liu: J. Comp. Neurol. 232:241-260, '85) and the AII/Gly2 of cat retina (Famiglietti and Kolb: Brain Res. 84:293-300, '75; Pourcho and Goebel: J. Comp. Neurol. 233:473-480, '85a). Gly+ amacrines synapse most frequently onto Gly- amacrines and both Gly- and Gly+ bipolars. Gly+ bipolar cells appeared to be cone bipolars because their labeled dendrites could be traced only to cone pedicles. The pattern of these labeled dendritic trees indicated that both diffuse and midget types of biopolars were Gly+. The EM distribution of labeled synapses showed Gly+ amacrine synapses throughout the IPL, but these composed only 11-23% of the amacrine population. Most of the Gly+ bipolar terminals were in the inner IPL, where 70% of all bipolar terminals were labeled. These findings are consistent with previous data from cats and humans and suggest that both amacrine and bipolar cells contribute to glycine-mediated neurotransmission in the monkey retina.

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Year:  1988        PMID: 3209734     DOI: 10.1002/cne.902730404

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


  14 in total

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3.  Amino acid signatures in the primate retina.

Authors:  M Kalloniatis; R E Marc; R F Murry
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4.  Neurotransmitter coupling through gap junctions in the retina.

Authors:  D I Vaney; J C Nelson; D V Pow
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5.  GABAergic and glycinergic IPSCs in ganglion cells of rat retinal slices.

Authors:  D A Protti; H M Gerschenfeld; I Llano
Journal:  J Neurosci       Date:  1997-08-15       Impact factor: 6.167

6.  The number of unidentified amacrine cells in the mammalian retina.

Authors:  E Strettoi; R H Masland
Journal:  Proc Natl Acad Sci U S A       Date:  1996-12-10       Impact factor: 11.205

7.  Morphology and connectivity of the small bistratified A8 amacrine cell in the mouse retina.

Authors:  Sammy C S Lee; Arndt Meyer; Timm Schubert; Laura Hüser; Karin Dedek; Silke Haverkamp
Journal:  J Comp Neurol       Date:  2015-03-10       Impact factor: 3.215

8.  Amino acid receptors of midget and parasol ganglion cells in primate retina.

Authors:  Z J Zhou; D W Marshak; G L Fain
Journal:  Proc Natl Acad Sci U S A       Date:  1994-05-24       Impact factor: 11.205

9.  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

10.  Colocalization of glutamate and glycine in bipolar cell terminals of the human retina.

Authors:  S Davanger; J Storm-Mathisen; O P Ottersen
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

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