Evidence map›Paper›PMID 12417648›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2002

Microglia-Müller glia cell interactions control neurotrophic factor production during light-induced retinal degeneration.

Takayuki Harada, Chikako Harada, Shinichi Kohsaka, Etsuko Wada, Kazuhiko Yoshida, Shigeaki Ohno, Hiroshi Mamada, Kohichi Tanaka, Luis F Parada, Keiji Wada

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 176 papers.

0numbers the graph read from it
0cells of the map it votes in
176citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

176 citing papers in PubMed, 388 citations in OpenAlex.

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  5. Minocycline treatment reduces the activation of mononuclear phagocytes and improves retinal function in a mouse model of Leber congenital amaurosis.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2025
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116 more citing papers are in PubMed but not listed here.

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

10 authors at 5 institutions in 3 countries.

Takayuki HaradaDepartment of Degenerative Neurological Diseases, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo 187-8502, Japan.harada.aud@mri.tmd.ac.jp
Chikako Harada
Shinichi Kohsaka
Etsuko Wada
Kazuhiko Yoshida
Shigeaki Ohno
Hiroshi Mamada
Kohichi Tanaka
Luis F Parada
Keiji Wada
Tokyo Medical and Dental University · JPGerman Center for Neurodegenerative Diseases · DEHokkaido University · JPFoundation Center · USNational Center of Neurology and Psychiatry · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Activation of microglia commonly occurs in response to a wide variety of pathological stimuli including trauma, axotomy, ischemia, and degeneration in the CNS. In the retina, prolonged or high-intensity exposure to visible light leads to photoreceptor cell apoptosis. In such a light-reared retina, we found that activated microglia invade the degenerating photoreceptor layer and alter expression of neurotrophic factors such as nerve growth factor (NGF), ciliary neurotrophic factor (CNTF), and glial cell line-derived neurotrophic factor (GDNF). Because these neurotrophic factors modulate secondary trophic factor expression in Müller glial cells, microglia-Müller glia cell interaction may contribute to protection of photoreceptors or increase photoreceptor apoptosis. In the present study, we demonstrate the possibility that such functional glia-glia interactions constitute the key mechanism by which microglia-derived NGF, brain-derived neurotrophic factor (BDNF), and CNTF indirectly influence photoreceptor survival, although the receptors for these neurotrophic factors are absent from photoreceptors, by modulating basic fibroblast growth factor (bFGF) and GDNF production and release from Müller glia. These observations suggest that microglia regulate the microglia-Müller glia-photoreceptor network that serves as a trophic factor-controlling system during retinal degeneration.

Indexed as

AnimalsBrain-Derived Neurotrophic FactorCell MovementCells, CulturedCiliary Neurotrophic FactorDisease Models, AnimalGlial Cell Line-Derived Neurotrophic FactorLightMiceMice, Inbred C57BLMice, KnockoutMicrogliaNerve Growth FactorNerve Growth FactorsNeurogliaNeurotrophin 3Brain-Derived Neurotrophic FactorCiliary Neurotrophic FactorGdnf protein, mouseGdnf protein, ratGlial Cell Line-Derived Neurotrophic FactorNerve Growth FactorNerve Growth FactorsNeurotrophin 3Receptor, Nerve Growth FactorReceptors, Nerve Growth FactorRNA, Messenger

Identifiers

PMID12417648
PMCPMC6758038
OpenAlexW1861582625

What OpenQuestion holds

Textmetadata
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.