Evidence map›Paper›PMID 26631939›Full record

ArticleScientific reports2015

microRNA targeting of the P2X7 purinoceptor opposes a contralateral epileptogenic focus in the hippocampus.

Eva M Jimenez-Mateos, Marina Arribas-Blazquez, Amaya Sanz-Rodriguez, Caoimhin Concannon, Luis A Olivos-Ore, Cristina R Reschke, Claire M Mooney, Catherine Mooney, Eleonora Lugara, James Morgan and 12 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
10.1field-weighted citation impact, top 1% 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

55 citing papers in PubMed, 109 citations in OpenAlex.

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  14. The P2X7 Receptor as a Mechanistic Biomarker for Epilepsy.International journal of molecular sciences · 2023
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  20. Analyzing the Role of the P2X7 Receptor in Epilepsy.Methods in molecular biology (Clifton, N.J.) · 2022
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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

22 authors at 4 institutions in 3 countries.

Eva M Jimenez-MateosDepartment of Physiology &Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
Marina Arribas-BlazquezDepartment of Toxicology and Pharmacology, Faculty of Veterinary Medicine, Universidad Complutense de Madrid, Madrid, Spain.
Amaya Sanz-RodriguezDepartment of Physiology &Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
Caoimhin ConcannonDepartment of Physiology &Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
Luis A Olivos-OreDepartment of Toxicology and Pharmacology, Faculty of Veterinary Medicine, Universidad Complutense de Madrid, Madrid, Spain.
Cristina R ReschkeDepartment of Physiology &Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
Claire M MooneyDepartment of Physiology &Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
Catherine MooneyDepartment of Physiology &Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
Eleonora LugaraDepartment of Physiology &Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
James MorganDepartment of Physiology &Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
Elena LangaDepartment of Physiology &Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
Alba Jimenez-PachecoDepartment of Physiology &Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
Luiz Fernando Almeida SilvaDepartment of Physiology &Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
Guillaume MesuretDepartment of Physiology &Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
Detlev BoisonRobert S. Dow Neurobiology Laboratories, Legacy Research Institute, Portland, OR, USA.
M Teresa Miras-PortugalDepartment of Biochemistry, Faculty of Veterinary Medicine, Universidad Complutense de Madrid, Madrid, Spain.
Michael LetavicJanssen Research &Development, LLC, Neuroscience, 3210 Merryfield Row, San Diego, CA 92121, San Diego, USA.
Antonio R ArtalejoDepartment of Toxicology and Pharmacology, Faculty of Veterinary Medicine, Universidad Complutense de Madrid, Madrid, Spain.
Anindya BhattacharyaJanssen Research &Development, LLC, Neuroscience, 3210 Merryfield Row, San Diego, CA 92121, San Diego, USA.
Miguel Diaz-HernandezDepartment of Biochemistry, Faculty of Veterinary Medicine, Universidad Complutense de Madrid, Madrid, Spain.
David C HenshallDepartment of Physiology &Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
Tobias EngelDepartment of Physiology &Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
Royal College of Surgeons in Ireland · IEUniversidad Complutense de Madrid · ESJanssen (United States) · USLegacy Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ATP-gated ionotropic P2X7 receptor (P2X7R) modulates glial activation, cytokine production and neurotransmitter release following brain injury. Levels of the P2X7R are increased in experimental and human epilepsy but the mechanisms controlling P2X7R expression remain poorly understood. Here we investigated P2X7R responses after focal-onset status epilepticus in mice, comparing changes in the damaged, ipsilateral hippocampus to the spared, contralateral hippocampus. P2X7R-gated inward currents were suppressed in the contralateral hippocampus and P2rx7 mRNA was selectively uploaded into the RNA-induced silencing complex (RISC), suggesting microRNA targeting. Analysis of RISC-loaded microRNAs using a high-throughput platform, as well as functional assays, suggested the P2X7R is a target of microRNA-22. Inhibition of microRNA-22 increased P2X7R expression and cytokine levels in the contralateral hippocampus after status epilepticus and resulted in more frequent spontaneous seizures in mice. The major pro-inflammatory and hyperexcitability effects of microRNA-22 silencing were prevented in P2rx7(-/-) mice or by treatment with a specific P2X7R antagonist. Finally, in vivo injection of microRNA-22 mimics transiently suppressed spontaneous seizures in mice. The present study supports a role for post-transcriptional regulation of the P2X7R and suggests therapeutic targeting of microRNA-22 may prevent inflammation and development of a secondary epileptogenic focus in the brain.

Indexed as

AnimalsAstrocytesElectroencephalographyGene Expression RegulationHippocampusInflammationMaleMice, Inbred C57BLMicroRNAsReceptors, Purinergic P2X7RNA-Induced Silencing ComplexRNA InterferenceStatus EpilepticusMicroRNAsMirn22 microRNA, mouseReceptors, Purinergic P2X7RNA-Induced Silencing Complex

Identifiers

PMID26631939
PMCPMC4668358
OpenAlexW2421958998

What OpenQuestion holds

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LicenceCC BY
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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.