Evidence map›Paper›PMID 24710318›Full record

ArticleScientific reports2014

Microglia trigger astrocyte-mediated neuroprotection via purinergic gliotransmission.

Youichi Shinozaki, Masatoshi Nomura, Ken Iwatsuki, Yoshinori Moriyama, Christian Gachet, Schuichi Koizumi

Abstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing 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

57 citing papers in PubMed.

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  15. Astrocyte Immune Functions and Glaucoma.International journal of molecular sciences · 2023
    Review
  16. Minocycline prevents hypoxia-induced seizures.Frontiers in neural circuits · 2023
    Article
  17. 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

6 authors.

Youichi Shinozaki1] Department of Neuropharmacology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, 1110 Shimokato, Chuo, Yamanashi 409-3898, Japan [2] Japan Science and Technology Agency, CREST, Tokyo 102-0076, Japan.
Masatoshi NomuraDepartment of Endocrine and Metabolic Diseases/Diabetes Mellitus Kyushu University Hospital, Fukuoka 812-8582, Japan.
Ken IwatsukiInstitute for Innovation, Ajinomoto Co. Inc., Kawasaki 210-8681, Japan.
Yoshinori MoriyamaAdvanced Science Research Center, Okayama University, Okayama 700-8530, Japan.
Christian GachetInstitut National de la Santé et de la Recherche Médicale (INSERM), U.311, Etablissement de Transfusion Sanguine, 10, rue Spielmann, B.P. 36, 67065 Strasbourg, France.
Schuichi Koizumi1] Department of Neuropharmacology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, 1110 Shimokato, Chuo, Yamanashi 409-3898, Japan [2] Japan Science and Technology Agency, CREST, Tokyo 102-0076, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microglia are highly sensitive to even small changes in the brain environment, such as invasion of non-hazardous toxicants or the presymptomatic state of diseases. However, the physiological or pathophysiological consequences of their responses remain unknown. Here, we report that cultured microglia sense low concentrations of the neurotoxicant methylmercury (MeHg(low)) and provide neuroprotection against MeHg, for which astrocytes are also required. When exposed to MeHg(low), microglia exocytosed ATP via p38 MAPK- and vesicular nucleotide transporter (VNUT)-dependent mechanisms. Astrocytes responded to the microglia-derived ATP via P2Y1 receptors and released interleukin-6 (IL-6), thereby protecting neurons against MeHg(low). These neuroprotective actions were also observed in organotypic hippocampal slices from wild-type mice, but not in slices prepared from VNUT knockout or P2Y1 receptor knockout mice. These findings suggest that microglia sense and respond to even non-hazardous toxicants such as MeHg(low) and change their phenotype into a neuroprotective one, for which astrocytic support is required.

Indexed as

Synaptic TransmissionAdenosine TriphosphateAnimalsAstrocytesCalcium SignalingCell CommunicationCells, CulturedExocytosisHippocampusInterleukin-6Methylmercury CompoundsMiceMice, KnockoutMicrogliaNeuronsNucleotide Transport ProteinsAdenosine TriphosphateInterleukin-6Methylmercury CompoundsNucleotide Transport Proteinsp38 Mitogen-Activated Protein KinasesReceptors, Purinergic P2Y1

Identifiers

PMID24710318
PMCPMC3948352

What OpenQuestion holds

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Registered trials

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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.