Literature DB >> 2903868

Two types of tyrosine hydroxylase-immunoreactive amacrine cell in the rhesus monkey retina.

A P Mariani1, J N Hokoc.   

Abstract

Two types of amacrine cell immunoreactive for tyrosine hydroxylase (TH), the rate-limiting enzyme in the catecholamine (CA)-synthetic pathway, are described in the rhesus monkey retina with the indirect-immunofluorescent method. These 2 types of neuron differ in soma size, plane of arborization in the inner plexiform layer, levels of the enzyme TH as quantified by microspectrofluorometry, and population density. Type 1 CA cells have comparatively large cell bodies almost exclusively in the innermost row of the inner nuclear layer; their processes arborize in the outermost stratum of the inner plexiform layer; they give rise to fine predominantly radially oriented fibers in the inner nuclear layer; and there are about 26 type 1 CA cells/mm2. Type 2 CA amacrine cells have relatively small cell bodies located in the inner nuclear layer (44.4%), the inner plexiform layer (35.6%) and the ganglion cell layer (20%), and their processes arborize in the center of the inner plexiform layer. Although type 2 CA amacrine cells are more numerous (35 cells/mm2) than type 1 CA cells, type 1 CA amacrine cells are 3.5 x brighter than type 2 CA cells and therefore likely to contain 3.5 X more TH. Thus the primate retina contains 2 distinct catecholaminergic neuronal pathways that could have different functional roles in vision.

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Year:  1988        PMID: 2903868     DOI: 10.1002/cne.902760106

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


  18 in total

1.  Immunohistochemical identification and synaptic inputs to the diffuse bipolar cell type DB1 in macaque retina.

Authors:  Theresa Puthussery; Jacqueline Gayet-Primo; W Rowland Taylor; Silke Haverkamp
Journal:  J Comp Neurol       Date:  2011-12-15       Impact factor: 3.215

2.  Amacrine cell subtypes differ in their intrinsic neurite growth capacity.

Authors:  Noelia J Kunzevitzky; Kevin T Willeford; William J Feuer; Monica V Almeida; Jeffrey L Goldberg
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-11-15       Impact factor: 4.799

3.  Spontaneous activity of solitary dopaminergic cells of the retina.

Authors:  A Feigenspan; S Gustincich; B P Bean; E Raviola
Journal:  J Neurosci       Date:  1998-09-01       Impact factor: 6.167

4.  Somatic and neuritic spines on tyrosine hydroxylase-immunopositive cells of rat retina.

Authors:  Anna Fasoli; James Dang; Jeffrey S Johnson; Aaron H Gouw; Alex Fogli Iseppe; Andrew T Ishida
Journal:  J Comp Neurol       Date:  2017-02-13       Impact factor: 3.215

5.  Molecular Classification and Comparative Taxonomics of Foveal and Peripheral Cells in Primate Retina.

Authors:  Yi-Rong Peng; Karthik Shekhar; Wenjun Yan; Dustin Herrmann; Anna Sappington; Gregory S Bryman; Tavé van Zyl; Michael Tri H Do; Aviv Regev; Joshua R Sanes
Journal:  Cell       Date:  2019-01-31       Impact factor: 41.582

Review 6.  From random to regular: Variation in the patterning of retinal mosaics.

Authors:  Patrick W Keeley; Stephen J Eglen; Benjamin E Reese
Journal:  J Comp Neurol       Date:  2020-03-03       Impact factor: 3.215

7.  Laminin deficits induce alterations in the development of dopaminergic neurons in the mouse retina.

Authors:  Viktória Dénes; Paul Witkovsky; Manuel Koch; Dale D Hunter; Germán Pinzón-Duarte; William J Brunken
Journal:  Vis Neurosci       Date:  2007-08-22       Impact factor: 3.241

8.  Light regulation of retinal dopamine that is independent of melanopsin phototransduction.

Authors:  M A Cameron; N Pozdeyev; A A Vugler; H Cooper; P M Iuvone; R J Lucas
Journal:  Eur J Neurosci       Date:  2009-02-06       Impact factor: 3.386

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.  New mouse lines for the analysis of neuronal morphology using CreER(T)/loxP-directed sparse labeling.

Authors:  Tudor C Badea; Zhong L Hua; Philip M Smallwood; John Williams; Thomas Rotolo; Xin Ye; Jeremy Nathans
Journal:  PLoS One       Date:  2009-11-16       Impact factor: 3.240

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