Evidence map›Paper›PMID 21880927›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2011

Overexpression of neurotrophin-3 stimulates a second wave of dopaminergic amacrine cell genesis after birth in the mouse retina.

Miho Yoshida, Liang Feng, François Grimbert, Krsna V Rangarajan, William Buggele, David R Copenhagen, Jianhua Cang, Xiaorong Liu

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 43% of its field
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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Prolonged Light Exposure Induces Long-Lasting Retinal Wave Plasticity via Retrograde Melanopsin-Dopamine Signaling.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
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  7. Retinal Waves Modulate an Intraretinal Circuit of Intrinsically Photosensitive Retinal Ganglion Cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
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  11. Intrinsically photosensitive ganglion cells contribute to plasticity in retinal wave circuits.Proceedings of the National Academy of Sciences of the United States of America · 2013
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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

8 authors at 4 institutions in 2 countries.

Miho YoshidaDepartment of Neurobiology and Physiology, Northwestern University, Evanston, Illinois 60208, USA.
Liang Feng
François Grimbert
Krsna V Rangarajan
William Buggele
David R Copenhagen
Jianhua Cang
Xiaorong Liu
Northwestern University · USInstitute of Neurobiology · BGOphthalmology Associates (United States) · USUniversity of California, San Francisco · US

Funding

SYNAPTIC INTERACTIONS AND PROCESSES IN THE RETINAR01EY001869 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COPENHAGEN, DAVID RICHARD · 1985 to 2013
$3.9M
Topographic Maps and Visual Cortical FunctionsR01EY018621 · NEI · NORTHWESTERN UNIVERSITY · PI CANG, JIANHUA · 2008 to 2011
$1.5M
Neurotrophic Mechanisms in Retinal Ganglion Cell MaturationR01EY019034 · NEI · NORTHWESTERN UNIVERSITY · PI LIU, XIAORONG · 2008 to 2011
$1.4M
NEI NIH HHS R01 EY001869NEI NIH HHS R01EY001869NEI NIH HHS R01 EY018621NEI NIH HHS R01 EY019034
6 · The paper itself

Abstract

Dopaminergic amacrine (DA) cells play multiple and important roles in retinal function. Neurotrophins are known to modulate the number and morphology of DA cells, but the underlying regulatory mechanisms are unclear. Here, we investigate how neurotrophin-3 (NT-3) regulates DA cell density in the mouse retina. We demonstrate that overexpression of NT-3 upregulates DA cell number and leads to a consequent increase in the density of DA cell dendrites. To examine the mechanisms of DA cell density increase, we further investigate the effect of NT-3 overexpression on retinal apoptosis and mitosis during development. We find that NT-3 does not affect the well known wave of retinal cell apoptosis that normally occurs during the first 2 weeks after birth. Instead, overexpression of NT-3 promotes additional mitosis of DA cells at postnatal day 4, but does not affect cell mitosis before birth, the peak period of amacrine cell genesis in wild-type retinas. We next show that retinal explants cultured from birth to day 7 without extra NT-3 produced by lens exhibit similar number of DA cells as in wild type, further supporting the notion that postnatal overexpression of lens-derived NT-3 affects DA cell number. Moreover, the additional mitosis after birth in NT-3-overexpressing mice does not occur in calretinin-positive amacrine cells or PKC-positive rod ON bipolar cells. Thus, the NT-3-triggered wave of cell mitosis after birth is specific for the retinal DA cells.

Indexed as

Amacrine CellsAnimalsAnimals, NewbornBromodeoxyuridineCalbindin 2Cell CycleCell DeathDopamineGene Expression Regulation, DevelopmentalIn Situ Nick-End LabelingMiceMice, Inbred C57BLMice, TransgenicNeurogenesisNeurotrophin 3Protein Kinase CBromodeoxyuridineCalb2 protein, mouseCalbindin 2DopamineNeurotrophin 3Protein Kinase CS100 Calcium Binding Protein GTyrosine 3-Monooxygenase

Identifiers

PMID21880927
PMCPMC3184017
OpenAlexW2055891318

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.