Evidence map›Paper›PMID 40725219›Full record

ArticleInternational journal of molecular sciences2025

Comparative Analysis of Tyrosine Hydroxylase Amacrine Cells in the Mammalian Retina: Distribution and Quantification in Mouse, Rat, Ground Squirrel and Macaque Retinas.

Kiyoharu J Miyagishima, Xiaomin Lai, Amurta Nath, William N Grimes, Xiyuan Ping, Jeffrey S Diamond, Morven A Cameron, Wei Li, Francisco M Nadal-Nicolás

Abstract readComparative Study
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Kiyoharu J MiyagishimaRetinal Neurophysiology Section, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0002-9744-3152
Xiaomin LaiSomatosensation and Pain Unit, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, USA.
Amurta NathSynaptic Physiology Section, National Institute of Neurological Disease and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0002-7009-6883
William N GrimesSynaptic Physiology Section, National Institute of Neurological Disease and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
Xiyuan PingRetinal Neurophysiology Section, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Jeffrey S DiamondSynaptic Physiology Section, National Institute of Neurological Disease and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
Morven A CameronSchool of Medicine, Western Sydney University, Sydney, NSW 2560, Australia.
Wei LiRetinal Neurophysiology Section, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Francisco M Nadal-NicolásRetinal Neurophysiology Section, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0003-4121-514X

Funding

Functions of the Synaptic Ribbon in Retinal NeuronsZIAEY000488 · NEI · NATIONAL EYE INSTITUTE · PI LI, WEI · 2009 to 2025
$22.0M
Organization and development of the S-cone systemZIAEY000502 · NEI · NATIONAL EYE INSTITUTE · PI LI, WEI · 2010 to 2025
$12.6M
Fundación Séneca, Agencia de Ciencia y Tecnología Región de Murcia 22395/SF/23Intramural NIH HHS ZIA EY000488Intramural NIH HHS ZIA EY000502NIH HHS 1ZIAEY000488-16
6 · The paper itself

Abstract

Dopaminergic amacrine cells (DACs) are a subclass of amacrine cells that modulate retinal processing and light adaptation by releasing dopamine. Although the role of dopamine is largely conserved, their retinal distribution across mammals remains incompletely characterized. In mice, rats, thirteen-lined ground squirrels (TLGSs), and macaques, we systematically compared the localization, number, and topography of DACs by their expression of tyrosine hydroxylase (TH), a crucial enzyme in the biosynthesis of dopamine. In all species examined, TH+ cells were primarily located in the inner nuclear layer; however, there was a species-dependent influence on their number and distribution. Mice exhibited the highest density of TH+cells but completely lacked displaced TH+cells (dTH+cells) in the ganglion cell layer. Despite interspecies variation in the total number of TH+cells in the retina, the overall density in rats, TLGSs, and macaques was similar. Most species displayed a higher density of DACs toward central retinal regions. However, rats exhibited a distinctive dorsal concentration, particularly among dTH+cells. Although most species examined exhibited a similar ratio of TH+cells to Brn3a+ retinal ganglion cells, TLGSs showed a marked reduction, indicating a potentially diminished dopaminergic modulatory role. Species-specific DAC topographies aligned with specialized visual regions, such as the visual streak in TLGS and the macula in macaques. These results reveal both conserved and divergent features of retinal dopamine circuitry, reflecting evolutionary adaptations to visual processing demands.

Indexed as

Amacrine CellsRetinaTyrosine 3-MonooxygenaseAnimalsDopamineMacacaMaleMiceRatsRetinal Ganglion CellsSciuridaeSpecies SpecificityDopamineTyrosine 3-Monooxygenaseamacrine cellcell densitydopaminemammalian retinamonkeyretinal ganglion cellsspatial distributiontopographytyrosine hydroxylase

Identifiers

PMID40725219
PMCPMC12295965

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.