Evidence map›Paper›PMID 28090150›Full record

ReviewMediators of inflammation2016

M1 and M2 Functional Imprinting of Primary Microglia: Role of P2X7 Activation and miR-125b.

Chiara Parisi, Giulia Napoli, Pablo Pelegrin, Cinzia Volonté

Open access · goldAbstract readReview
In one paragraph

Review in Mediators of inflammation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
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  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
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  14. Article
  15. Review
  16. Review
  17. MicroRNAs in amyotrophic lateral sclerosis: from pathogenetic involvement to diagnostic biomarker and therapeutic agent development.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2020
    Review
  18. Dissection of P2X4 and P2X7 Receptor Current Components in BV-2 Microglia.International journal of molecular sciences · 2020
    Article
  19. Article
  20. P2X7 Receptors Amplify CNS Damage in Neurodegenerative Diseases.International journal of molecular sciences · 2020
    Review
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

4 authors at 2 institutions in 2 countries.

Chiara ParisiCNR-Institute of Cell Biology and Neurobiology, Via del Fosso di Fiorano 65, 00143 Rome, Italy; Fondazione Santa Lucia, Via del Fosso di Fiorano 65, 00143 Rome, Italy.
Giulia NapoliFondazione Santa Lucia, Via del Fosso di Fiorano 65, 00143 Rome, Italy.
Pablo PelegrinInflammation and Experimental Surgery Unit, CIBERehd, Biomedical Research Institute of Murcia (IMIB-Arrixaca), Clinical University Hospital Virgen de la Arrixaca, 30120 Murcia, Spain.ORCID 0000-0002-9688-1804
Cinzia VolontéCNR-Institute of Cell Biology and Neurobiology, Via del Fosso di Fiorano 65, 00143 Rome, Italy; Fondazione Santa Lucia, Via del Fosso di Fiorano 65, 00143 Rome, Italy.ORCID 0000-0001-7362-8307
Fondazione Santa Lucia · ITCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas · ES

Funding

European Research Council 614578
6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is a most frequently occurring and severe form of motor neuron disease, causing death within 3-5 years from diagnosis and with a worldwide incidence of about 2 per 100,000 person-years. Mutations in over twenty genes associated with familial forms of ALS have provided insights into the mechanisms leading to motor neuron death. Moreover, mutations in two RNA binding proteins, TAR DNA binding protein 43 and fused in sarcoma, have raised the intriguing possibility that perturbations of RNA metabolism, including that of the small endogenous RNA molecules that repress target genes at the posttranscriptional level, that is, microRNAs, may contribute to disease pathogenesis. At present, the mechanisms by which microglia actively participate to both toxic and neuroprotective actions in ALS constitute an important matter of research. Among the pathways involved in ALS-altered microglia responses, in previous works we have uncovered the hyperactivation of P2X7 receptor by extracellular ATP and the overexpression of miR-125b, both leading to uncontrolled toxic M1 reactions. In order to shed further light on the complexity of these processes, in this short review we will describe the M1/M2 functional imprinting of primary microglia and a role played by P2X7 and miR-125b in ALS microglia activation.

Indexed as

Amyotrophic Lateral SclerosisAnimalsBrain-Derived Neurotrophic FactorHumansInflammationMacrophagesMiceMicrogliaMicroRNAsMotor NeuronsMutationPhenotypeReceptors, Purinergic P2X7Signal TransductionSuperoxide DismutaseBDNF protein, humanBrain-Derived Neurotrophic FactorMicroRNAsMIRN125 microRNA, humanMirn125 microRNA, mouseP2RX7 protein, humanReceptors, Purinergic P2X7Superoxide Dismutase

Identifiers

PMID28090150
PMCPMC5206439
OpenAlexW2562241370

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.