Evidence map›Paper›PMID 27544384›Full record

ArticlePurinergic signalling2016

A new role for the P2Y-like GPR17 receptor in the modulation of multipotency of oligodendrocyte precursor cells in vitro.

Marta Boccazzi, Davide Lecca, Davide Marangon, Fabio Guagnini, Maria P Abbracchio, Stefania Ceruti

Open access · greenAbstract read
In one paragraph

Article in Purinergic signalling, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. NG2-glia crosstalk with microglia in health and disease.CNS neuroscience & therapeutics · 2022
    Review
  3. Article
  4. Involvement of GPR17 in Neuronal Fibre Outgrowth.International journal of molecular sciences · 2021
    Article
  5. Article
  6. Article
  7. GPR17 mediates ischemia-like neuronal injury via microglial activation.International journal of molecular medicine · 2018
    Article
  8. Review
  9. 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

6 authors at 2 institutions in 1 country.

Marta BoccazziLaboratory of Molecular and Cellular Pharmacology of Purinergic Transmission-Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, via Balzaretti, 9, 20133, Milan, Italy.
Davide LeccaLaboratory of Molecular and Cellular Pharmacology of Purinergic Transmission-Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, via Balzaretti, 9, 20133, Milan, Italy.
Davide MarangonLaboratory of Molecular and Cellular Pharmacology of Purinergic Transmission-Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, via Balzaretti, 9, 20133, Milan, Italy.
Fabio GuagniniSanofi Midy Research Center-Exploratory Unit Sanofi R&D, via G. Sbodio, 2, 20100, Milan, Italy.
Maria P AbbracchioLaboratory of Molecular and Cellular Pharmacology of Purinergic Transmission-Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, via Balzaretti, 9, 20133, Milan, Italy.
Stefania CerutiLaboratory of Molecular and Cellular Pharmacology of Purinergic Transmission-Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, via Balzaretti, 9, 20133, Milan, Italy. stefania.ceruti@unimi.it.ORCID 0000-0003-1663-4211
University of Milan · ITSanofi (Italy) · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oligodendrocyte precursor cells (OPCs, also called NG2 cells) are scattered throughout brain parenchyma, where they function as a reservoir to replace lost or damaged oligodendrocytes, the myelin-forming cells. The hypothesis that, under some circumstances, OPCs can actually behave as multipotent cells, thus generating astrocytes and neurons as well, has arisen from some in vitro and in vivo evidence, but the molecular pathways controlling this alternative fate of OPCs are not fully understood. Their identification would open new opportunities for neuronal replace strategies, by fostering the intrinsic ability of the brain to regenerate. Here, we show that the anti-epileptic epigenetic modulator valproic acid (VPA) can promote the generation of new neurons from NG2

Indexed as

AnimalsCell LineageCerebral CortexMultipotent Stem CellsNeural Stem CellsNeurogenesisNeuronsOligodendrogliaRatsRats, Sprague-DawleyReceptors, G-Protein-CoupledGPR17 protein, ratReceptors, G-Protein-CoupledGPR17NeurogenesisNG2 cellsOligodendrocyte precursor cellsValproic acid

Identifiers

PMID27544384
PMCPMC5124007
OpenAlexW2517535802

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.